<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>2nd PUC &#8211; KTBS Solutions</title>
	<atom:link href="https://ktbssolutions.com/category/2nd-puc/feed/" rel="self" type="application/rss+xml" />
	<link>https://ktbssolutions.com</link>
	<description>Karnataka State Board Textbook Solutions</description>
	<lastBuildDate>Wed, 15 Jul 2026 10:50:21 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.0.4</generator>
<site xmlns="com-wordpress:feed-additions:1">186551568</site>	<item>
		<title>2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics</title>
		<link>https://ktbssolutions.com/2nd-puc-chemistry-question-bank-chapter-4/</link>
		
		<dc:creator><![CDATA[Prasanna]]></dc:creator>
		<pubDate>Tue, 14 Jul 2026 10:10:08 +0000</pubDate>
				<category><![CDATA[2nd PUC]]></category>
		<guid isPermaLink="false">https://ktbssolutions.com/?p=10244</guid>

					<description><![CDATA[You can Download Chapter 4 Chemical Kinetics Questions and Answers, Notes, 2nd PUC Chemistry Question Bank with Answers Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations. Karnataka 2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics 2nd PUC Chemistry Chemical Kinetics NCERT Textbook Questions and Answers Question [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>You can Download Chapter 4 Chemical Kinetics Questions and Answers, Notes, <a href="https://ktbssolutions.com/2nd-puc-chemistry-question-bank/">2nd PUC Chemistry Question Bank with Answers</a> Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations.</p>
<h2>Karnataka 2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics</h2>
<div class="OD">
<div class="IL">
<div id=":ks.av" class="Up pC">
<h3 class="n291pb uaxL4e">2nd PUC Chemistry Chemical Kinetics NCERT Textbook Questions and Answers</h3>
<p>Question 1.<br />
From the rate expression for the following reactions, determine their order of reaction and the dimensions of the rate constants.<br />
(i) 3NO(g) → N<sub>2</sub>O (g) Rate = K[NO]<sup>2</sup><br />
(ii) H<sub>2</sub>O<sub>2</sub> (aq) + 3I<sup>&#8211;</sup> (aq) + 2H<sup>+</sup> → 2H<sub>2</sub>O(l) +I<sub>3</sub><sup>&#8211;</sup><br />
Rate = K[H<sub>2</sub>O<sub>2</sub>][I<sup>&#8211;</sup>]<br />
(iii) CH<sub>3</sub>CHO (g) → CH<sub>4</sub> (g) + CO(g)<br />
Rate = K [CH<sub>3</sub>CHO]<sup>3/2</sup><br />
(iv) C<sub>2</sub>H<sub>5</sub>Cl (g) → C<sub>2</sub>H<sub>4</sub> (g) + HCl (g)<br />
Rate = K [C<sub>2</sub>H<sub>5</sub>Cl]<br />
Ans:<br />
(i) 2<br />
(ii) 2<br />
(iii) 3/2<br />
(iv) 1</p>
<p>Question 2.<br />
For the reaction:<br />
2A + B → A<sub>2</sub>B<br />
the rate = k[A][B]<sup>2</sup> with k = 2.0 × 10<sup>-6</sup> mol<sup>-2</sup> L<sup>2</sup> s<sup>-1</sup>. Calculate the initial rate of the reaction when [A] = 0.1 mol L<sup>-1</sup>, [B] = 0.2 mol L<sup>-1</sup>. Calculate the rate of reaction after [A] is reduced to 0.06 mol L<sup>-1</sup>.<br />
Answer:<br />
Initial rate = K [A] [B]<sup>2</sup><br />
= 2.0 × 10<sup>-6 </sup>(mol<sup>-2</sup> L<sup>2</sup> s<sup>-1</sup> × 0.1 (mol<sup>-1</sup>) × (0.2)<sup>2</sup>mol<sup>2</sup>L<sup>-2</sup><br />
= 8 × 10<sup>-9</sup> mol L<sup>-1</sup> s<sup>-1</sup><br />
we know that<br />
<img decoding="async" class="alignnone size-full wp-image-72250" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-1.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 1" width="283" height="80" /></p>
<p>\(\frac { 1 }{ 2 }\) [rate of disappearance of A] = rate of disappearance of B<br />
∴ When [A] is reduced by 0.1 &#8211; 0.06 = 0.04 M<br />
[B] is reduced by \(\frac { 1 }{ 2 }\) × 0.04 = 0.02 M<br />
∴ [B] remaining = 0.2 -0.02 = 0.18 M<br />
Rate of reaction = K [A] [B]<sup>2</sup><br />
= 2.0 × 10<sup>-6</sup> mol <sup>-2</sup> L<sup>21</sup><br />
s <sup>-1</sup> × 0.06 × (0.18)<sup>2</sup> mol<sup>3</sup> L<sup>-3</sup><br />
= 3.89 × 10<sup>-9</sup> Ms<sup>-1</sup></p>
<p>Question 3.<br />
The decomposition of NH<sub>3</sub>on platinum surface is zero order reaction. What are the rates of production of N<sub>2</sub> and H<sub>2</sub> if k = 2.5 × 10<sup>-4</sup>(H mol<sup>-1</sup>L s<sup>-1</sup> ?<br />
Answer:<br />
For zero order reaction rate of reaction = K<br />
<img decoding="async" class="alignnone size-full wp-image-72252" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-2.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 2" width="344" height="111" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-2.png 344w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-2-300x97.png 300w" sizes="(max-width: 344px) 100vw, 344px" /><br />
∴Rate of production of N<sub>2</sub>= k = 2.5 × 10<sup>-4</sup> Ms<sup>-1</sup><br />
Rate of production of H<sub>2</sub> = 3k<br />
= 3 × 2.5 × 10<sup>-4</sup><br />
= 7.5 × 10<sup>-4</sup> Ms<sup>-1</sup></p>
<p>Question 4.<br />
The decomposition of dimethyl ether leads to the formation of CH<sub>4</sub>, H<sub>2</sub> and CO and the reaction rate is given by<br />
Rate = K [CH<sub>3</sub>OCH<sub>3</sub>]<sup>3/2</sup><br />
The rate of reaction is followed by increase in pressure in a closed vessel, so the rate can also be expressed in terms of the partial pressure of dimethyl ether, i.e.<br />
Rate = k (P<sub>CH<sub>3</sub>OCH<sub>3</sub></sub>)<sup>3/2</sup><br />
If the pressure is measured in bar and time in minutes, then what are the units of rate and rate constants?<br />
Answer:<br />
Units rate of reaction = bar min<sup>-1</sup><br />
units of rate constant<br />
<img decoding="async" class="alignnone size-full wp-image-72254" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-3.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 3" width="296" height="122" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 5.<br />
Mention the factors that affect the rate of a chemical reaction.<br />
Answer:<br />
(i) Concentration of reactants<br />
(ii) Temperature<br />
(iii) Nature of reactants and products<br />
(iv) Exposure to light (Radiation)<br />
(v) presence of catalysts.</p>
<p>Question 6.<br />
A reaction is second order with respect to a reactant. How is the rate of reaction &#8216; affected if the concentration of the reactant is (i) doubled (ii) reduced to half ?<br />
Answer:<br />
(i) Four times<br />
[-rate<sub>1</sub> = K[C<sub>A</sub>]<sup>2</sup><br />
C<sub>A2</sub> = 2C<sub>A</sub><br />
rate<sub>2</sub> = K [2C<sub>A</sub>]<sup>2</sup> = 4K [C<sub>A</sub>]<sup>2</sup>] = 4 rate<sub>1</sub>]</p>
<p>(ii) 1/4 times<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72256" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-4.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 4" width="285" height="120" /></p>
<p>Question 7.<br />
What is the effect of temperature on the rate constant of a reaction ? How can this temperature effect on rate constant be represented quantitatively.<br />
Answer:<br />
Increasing the temperature on decreasing the activation energy will result in an increase in the rate of reaction and an exponential increase in the rate constant. On increasing the temperature the fraction of molecules which collide with energy greater than Ea increases and hence the rate constant (exponentially)<br />
K = A <sup>-ea/RT</sup> , quantitative representation of temperature effect on rate constant.</p>
<p>Question 8.<br />
In a pseudo first order hydrolysis of ester in water, the following results were obtained:</p>
<table border="2">
<tbody>
<tr>
<td width="126"><strong>t/s</strong></td>
<td width="60">0</td>
<td width="54">30</td>
<td width="48">60</td>
<td width="66">90</td>
</tr>
<tr>
<td width="126"><strong>[Ester]/mol L<sup>-1</sup></strong></td>
<td width="60">0.55</td>
<td width="54">0.31</td>
<td width="48">0.17</td>
<td width="66">0.085</td>
</tr>
</tbody>
</table>
<p>(i) Calculate the average rate of reaction between the time interval 30 to 60 seconds.<br />
(ii) Calculate the pseudo first order rate constant for the hydrolysis of ester.<br />
Answer:<br />
(i)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72258" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-5.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 5" width="318" height="129" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-5.png 318w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-5-300x122.png 300w" sizes="auto, (max-width: 318px) 100vw, 318px" /></p>
<p>(ii) For pseudo first order reaction,<br />
Average rate = Rate constant × Average concentration Average rate<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72261" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-6.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 6" width="376" height="137" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-6.png 376w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-6-300x109.png 300w" sizes="auto, (max-width: 376px) 100vw, 376px" /></p>
<p>Question 9.<br />
A reaction is first order in A and second order in B.<br />
(i) Write the differential rate equation.<br />
(ii) How is the rate affected on increasing the concentration of B three times?<br />
(iii) How is the rate affected when the concentrations of both A and B are doubled?<br />
Answer:<br />
(i)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72265" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-7.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 7" width="296" height="78" /><br />
(ii) When concentration of B is tripled, rate of reaction increases by 9 times.<br />
(iii) Rate of reaction increases by 8 times.</p>
<p>Question 10.<br />
In a reaction between A and B, the initial rate reaction (r<sub>0</sub>) was measured for different initial concentrations of A and B as given below.</p>
<table border="2">
<tbody>
<tr>
<td width="96">A/ mol L<sup>-1</sup></td>
<td width="78">0.20</td>
<td width="84">0.20</td>
<td width="78">0.40</td>
</tr>
<tr>
<td width="96">B/ mol L<sup>-1</sup></td>
<td width="78">0.30</td>
<td width="84">0.10</td>
<td width="78">0.05</td>
</tr>
<tr>
<td width="96">r<sub>θ</sub>mol L<sup>-1</sup>S<sup>-5</sup></td>
<td width="78">5.07&#215;10<sup>-5</sup></td>
<td width="84">5.07&#215;10<sup>-5</sup></td>
<td width="78">1.43 x 10<sup>-5</sup></td>
</tr>
</tbody>
</table>
<p>what is the order of the reaction with respect to A and B ?<br />
Answer:<br />
Let the rate law be, r = K [A]<sup>x</sup> [B]<sup>y</sup><br />
r<sub>1</sub> = K[0.2]<sup>x</sup>[0.3]<sup>y</sup> = 5.07 × 10<sup>-5</sup> -(1) .<br />
r<sub>2</sub> = K[0.2]<sup>x</sup> [0.1]<sup>y</sup> = 5.07 ×10<sup>-5</sup> -(2)<br />
r<sub>3</sub> = K [0.4]<sup>x</sup> [0.05]<sup>y</sup> = 7.6 × 10<sup>-5</sup> -(3) ,<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72273" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-8.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 8" width="341" height="242" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-8.png 341w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-8-300x213.png 300w" sizes="auto, (max-width: 341px) 100vw, 341px" /><br />
∴ The order of reaction with respect to A is 0.585 and with respect to B is 0.<br />
∴ rate law = K[A]<sup>0.858</sup> [B]<sup>0</sup> = K [A]<sup>0.585</sup>.</p>
<p>Question 11.<br />
The following results have been obtained during the kinetic studies of the reaction 2A + B → C + D</p>
<table border="2">
<tbody>
<tr>
<td style="text-align: center;" width="89"><strong>Experiment</strong></td>
<td style="text-align: center;" width="89"><strong>[A]/mol L<sup>-1</sup></strong></td>
<td style="text-align: center;" width="100"><strong>[B]/mol L<sup>-1</sup></strong></td>
<td style="text-align: center;" width="160"><strong>Initial rate of formation of D/mol L<sup>-1</sup>min<sup>-1</sup></strong></td>
</tr>
<tr>
<td width="89">I</td>
<td width="89">0.1</td>
<td width="100">0.1</td>
<td width="160">6.0 x 10<sup>-3</sup></td>
</tr>
<tr>
<td width="89">II</td>
<td width="89">0.3</td>
<td width="100">0.2</td>
<td width="160">7.2 x 10<sup>-2</sup></td>
</tr>
<tr>
<td width="89">III</td>
<td width="89">0.3</td>
<td width="100">0.4</td>
<td width="160">2.88 x 10<sup>-1</sup></td>
</tr>
<tr>
<td width="89">IV</td>
<td width="89">0.4</td>
<td width="100">0.1</td>
<td width="160">2.40 x 10<sup>-2</sup></td>
</tr>
</tbody>
</table>
<p>Determine the rate law and the rate constant for the reaction.<br />
Answer:<br />
r = K [A]<sup>x</sup> [B]<sup>y</sup><br />
r, = K[0.1]<sup>x</sup> [0.1]<sup>y</sup> = 6.0 × 10<sup>-3</sup> -(i)<br />
r2 = K [0.3]<sup>x</sup> [0.2]<sup>y</sup> = 7.2 × 10<sup>-2</sup> -(2)<br />
r3 = K [0.3]<sup>x</sup> [0.4]<sup>y</sup> = 2.88 × 10<sup>-1</sup> -(3)<br />
r4 = K [0.4]<sup>x</sup> [Q.l]<sup>y</sup> = 2.4 × 10<sup>-2</sup> -(4)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72275" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-9.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 9" width="296" height="57" /><br />
4<sup>x</sup> = 4<br />
⇒ x =1<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72277" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-10.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 10" width="336" height="57" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-10.png 336w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-10-300x51.png 300w" sizes="auto, (max-width: 336px) 100vw, 336px" /><br />
2<sup>y</sup> = 4 ⇒ y = 2.</p>
<p>∴ Rate law, r = K [A]<sup>1</sup> [B]<sup>2</sup><br />
Rate constant,<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72279" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-11.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 11" width="262" height="48" /><br />
= 6M<sup>-2</sup>min<sup>-1</sup></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 12.<br />
The reaction between A and B is first order with respect to A and zero order with respect to B. Fill in the blanks in the following table:</p>
<table border="2">
<tbody>
<tr>
<td style="text-align: center;" width="90"><strong>Experiment</strong></td>
<td style="text-align: center;" width="88"><strong>[A]/mol L<sup>-1</sup></strong></td>
<td style="text-align: center;" width="100"><strong>[B]/mol L<sup>-1</sup></strong></td>
<td style="text-align: center;" width="167"><strong>Initial rate /mol L<sup>-1 </sup>min<sup>-1</sup></strong></td>
</tr>
<tr>
<td width="90">I</td>
<td width="88">0.1</td>
<td width="100">0.1</td>
<td width="167">2.0 x 10<sup>-2</sup></td>
</tr>
<tr>
<td width="90">II</td>
<td width="88">x</td>
<td width="100">0.2</td>
<td width="167">4.0 x 10<sup>-2</sup></td>
</tr>
<tr>
<td width="90">III</td>
<td width="88">0.4</td>
<td width="100">0.4</td>
<td width="167">y</td>
</tr>
<tr>
<td width="90">IV</td>
<td width="88">z</td>
<td width="100">0.2</td>
<td width="167">2.0 x 10<sup>-2</sup></td>
</tr>
</tbody>
</table>
<p>Answer:<br />
rate law = K [A]<br />
from I 2.0 × 10<sup>-2</sup> = K 0.1<br />
⇒ K = 2.0 × 10<sup>-1</sup>min<sup>-1</sup><br />
from II 4 .0 × 10<sup>-2</sup> = 2 .0 × 10<sup>-31</sup> x<br />
⇒ K = 2 .0 × 10<sup>-1</sup> mol L<sup>-1</sup><br />
from III y = 2.0 × 10<sup>-1</sup> × 0.4<br />
⇒ y = 8 × 10<sup>-2</sup> mol 1L<br />
from IV 2.0 × 10<sup>-2</sup> = 2.0 × 10<sup>-1</sup> × z<br />
⇒ z = 0.1 mol L<sup>-1</sup>.</p>
<p>Question 13.<br />
Calculate the half &#8211; life of a first order reaction from their rate constants given below.<br />
(i) 200 s<sup>-1</sup><br />
(ii) 2 min<sup>-1</sup><br />
(iii) 4 years<sup>-1</sup><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72282" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-12.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 12" width="288" height="210" /></p>
<p>Question 14.<br />
The half-life for radioactive decay of 14C is 5730 years. An archaeological artifact containing wood had only 80% of the 14C found in a living tree. Estimate the age of the sample.<br />
Answer:<br />
[A]<sub>0</sub> = 100<br />
[A] = 80<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72298" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-13.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 13" width="291" height="185" /><br />
= 1845 years<br />
∴The age of the sample is 1845 years.</p>
<p>Question 15.<br />
The rate constant for a first order reaction is 60 s<sup>-1</sup>. How much time will it take to reduce the initial concentration of the reactant to its 1/16 th value?<br />
Answer:<br />
K = 60 s<sup>-1</sup><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72299" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-14.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 14" width="270" height="218" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 16.<br />
During nuclear explosion, one of the products is MSr with half-life of 28.1 years. If mg of <sup>90</sup>Sr was absorbed in the bones of a newly born baby instead of calcium, how much of it will remain after 10 years and 60 years if it is not lost metabolically ?<br />
Answer:<br />
t<sup>1/2</sup> = 28.1 years<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72311" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-15.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 15" width="307" height="62" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-15.png 307w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-15-300x61.png 300w" sizes="auto, (max-width: 307px) 100vw, 307px" /><br />
[A]<sub>0</sub> = 2.47 × 1μg<br />
For 10 years<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72312" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-16.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 16" width="316" height="259" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-16.png 316w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-16-300x246.png 300w" sizes="auto, (max-width: 316px) 100vw, 316px" /><br />
[A] =0.78 × 10<sup>-6</sup>g = 0.78μg<br />
For 60 years<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72317" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-17.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 17" width="254" height="317" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-17.png 254w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-17-240x300.png 240w" sizes="auto, (max-width: 254px) 100vw, 254px" /><br />
The amount of <sup>90</sup>Sr that will remain in the child’s body after 10 years is 0.78μg and after 60 years is 0.229 μg.</p>
<p>Question 17.<br />
For a first order reaction, show that time required for 99% completion is twice the time required for the completion of 90% of reaction.<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72319" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-18.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 18" width="149" height="63" /><br />
for 99% completion,<br />
if [A]<sub>0</sub> = 100<br />
[A] = 100-99= 1<br />
for 90% completion<br />
[A] = 100-99<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72321" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-19.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 19" width="320" height="328" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-19.png 320w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-19-293x300.png 293w" sizes="auto, (max-width: 320px) 100vw, 320px" /></p>
<p>Question 18.<br />
A first order reaction takes 40 min for 30% decomposition. Calculate t<sub>1/2</sub>.<br />
Answer:<br />
[A]<sub>0</sub> = 100.<br />
[A] = 100 &#8211; 30 = 70<br />
t = 40min<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72323" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-20.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 20" width="339" height="204" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-20.png 339w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-20-300x181.png 300w" sizes="auto, (max-width: 339px) 100vw, 339px" /></p>
<p>Question 19.<br />
The rate constant for the decomposition of hydrocarbons is 2.418 × 10<sup>-5</sup>s<sup>-1</sup> at 546 K. If the energy of activation is 179.9 kJ/mol, what will be the value of pre-exponential factor ?<br />
Answer:<br />
Pre &#8211; exponential factor = A = Arrhenius<br />
factor = frequency factor<br />
K = 2.418 × 10<sup>-5</sup>s<sup>-1</sup><br />
T = 546 K.<br />
Ea= 179.9 × 10<sup>-3</sup>J mol<sup>-1</sup><br />
[By Arrhenius equation] K = \(\text { Ae }^{-\mathrm{E}} / \mathrm{kr}\)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72334" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-21.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 21" width="324" height="224" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-21.png 324w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-21-300x207.png 300w" sizes="auto, (max-width: 324px) 100vw, 324px" /></p>
<p>Question 20.<br />
onsider a certain reaction A → Products with k = 2.0 × 10<sup>-2</sup> s<sup>-1</sup>. Calculate the concentration of A remaining after 100s if the initial concentration of A is 1.0 mol Lr1. Ans: [A]0 = 1 mol L<sup>-1</sup><br />
Answer:<br />
[A]<sub>0</sub> = 1 mol L<sup>-1</sup><br />
t = 100s<br />
k = 2.0 × 10<sup>-2</sup>s<sup>-1</sup><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72336" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-22.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 22" width="256" height="131" /><br />
log [A] = -0.8684<br />
⇒ [A] = 10 <sup>-0.8684</sup> = 0.354 mol L<sup>-1</sup></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 21.<br />
Sucrose decomposes in acid solution into glucose and fructose according to the first order rate law, with t<sup>1/2</sup> = 3.00 hours. What fraction of sample of sucrose remains after 8 hours ?<br />
Answer:<br />
t<sup>1/2</sup> = 3 hrs<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72338" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-23.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 23" width="314" height="242" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-23.png 314w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-23-300x231.png 300w" sizes="auto, (max-width: 314px) 100vw, 314px" /></p>
<p>Question 22.<br />
The decomposition of hydrocarbon follows the equation K = (1.5 × 10<sup>11</sup> s<sup>-1</sup>)<br />
\(e^{\frac{-28000 K}{T}}\) Calculate E<sub>a</sub><br />
Answer:<br />
According to Arrehenius equation<br />
K = Ae<sup>-Ea/RT</sup><br />
Given K = (4.5 × 10<sup>11</sup>s<sup>-1</sup>)\(e^{\frac{-28000 K}{T}}\)<br />
comparing the two equations<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72340" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-24.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 24" width="137" height="60" /><br />
E<sub>a</sub> = 28000 × R<br />
= 28000 × 8.314 J mol<sup>-1</sup><br />
= 232.79 KJ mol<sup>-1</sup>.</p>
<p>Question 23.<br />
The rate constant for the first order decomposition of H<sub>2</sub>O<sub>2</sub> is given by the following equation:<br />
log k = 14.34 &#8211; \(\frac{1.25 \times 10^{4} K}{\mathbf{T}}\)<br />
Calculate E<sub>a</sub> for this reaction and at what temperature will Its half-period be 256 minutes?<br />
Answer:<br />
According to Arrehenius equation<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72341" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-25.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 25" width="324" height="257" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-25.png 324w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-25-300x238.png 300w" sizes="auto, (max-width: 324px) 100vw, 324px" /><br />
E<sub>a</sub> = 2.303 R × 1.25 × 10<sup>4</sup> K<br />
= 2.303 × 8.3l4 JK<sup>-1</sup> mol<sup>-1</sup> × 1.25 × 10<sup>4</sup> K<br />
= 239.34 KJ mol<sup>-1</sup><br />
What t<sup>1/2</sup> = 356 min<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72343" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-26.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 26" width="301" height="53" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-26.png 301w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-26-300x53.png 300w" sizes="auto, (max-width: 301px) 100vw, 301px" /><br />
Substituting K in given equation<br />
log(4.51 × 10<sup>-5</sup>) = 14.34 &#8211; \(\frac{1.25 \times 10^{4}}{\mathrm{T}}\)<br />
T = 669 K.</p>
<p>Question 24.<br />
The decomposition of A into product has value of k as 4.5 × 10<sup>3</sup> s<sup>-1</sup> at 10°C and energy of activation 60 kj mol<sup>-1</sup>. At what temperature would k be 1.5 × 10<sup>4</sup>s<sup>-1</sup> ?<br />
Answer:<br />
k<sub>1</sub> = 4.5 × 10<sup>3</sup> s<sup>-1</sup><br />
k<sub>2</sub> = 1.5 × 10<sup>4</sup>s<sup>-1</sup><br />
E<sub>a</sub> = 60 × 10<sup>3</sup> J mol<sup>-1</sup><br />
R = 8.314 JK<sup>-1</sup> mol<sup>-1</sup><br />
T<sub>1</sub> = 283 k<br />
T<sub>2</sub> = ?<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72344" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-27.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 27" width="360" height="183" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-27.png 360w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-27-300x153.png 300w" sizes="auto, (max-width: 360px) 100vw, 360px" /></p>
<p>Question 25.<br />
The rate of a reaction quadruples when the temperature changes from 293 K to 313 K. Calculate the energy of activation of the reaction assuming that it does not change with temperature.<br />
Answer:<br />
T<sub>1</sub> = 283 k<br />
T<sub>2</sub> = 313 k<br />
k<sub>2</sub> = 4k<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72347" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-28.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 28" width="338" height="226" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-28.png 338w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-28-300x201.png 300w" sizes="auto, (max-width: 338px) 100vw, 338px" /></p>
<h3 class="n291pb uaxL4e">2nd PUC Chemistry Chemical Kinetics Additional Questions and Answers</h3>
<p>Question 1.<br />
Name the factors on which the rate of a particular reaction depends. (H. S .B 2001)<br />
Answer:<br />
Concentration, temperature, presence of catalyst and light, surface area of reactants.</p>
<p>Question 2.<br />
Write the expression for rate of reaction in terms of each reactant and product for the reaction.<br />
N<sub>2</sub> + 3H<sub>2</sub> → 2NH<sub>3</sub> (P.S.B 2011, HSB 2000)<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72352" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-29.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 29" width="279" height="52" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 3.<br />
Give the example of a reaction having fractional order. (PSB 2000)<br />
Answer:<br />
Decomposition of acetal dehyde (order =1.5)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72354" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-30.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 30" width="230" height="33" /></p>
<p>Question 4.<br />
Give an example of a psueudo first order reaction. (AISB, DSB 2004, DSB 2006)<br />
Answer:<br />
Acid catalysed hydrolysis of ethyl acetate<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72356" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-31.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 31" width="329" height="92" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-31.png 329w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-31-300x84.png 300w" sizes="auto, (max-width: 329px) 100vw, 329px" /><br />
Rate = K [CH3COOC2H5] [H20]°</p>
<p>Question 5.<br />
For an elementary reaction,<br />
2 A + B → 3C<br />
the rate of appearance of C at time ‘t’ is 1.3 × 10<sup>4</sup> mol<sup>-1</sup> S<sup>-1</sup>. Calculate at this time<br />
(i) Rate of the reaction<br />
(ii) Rate of disappearance of A. (CBSE sample paper II 2008)<br />
Answer:<br />
Rate<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72357" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-32.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 32" width="289" height="160" /><br />
= 1/3 × 1.3 × 10<sup>-4</sup>mol L<sup>-1</sup>S<sup>-1</sup><br />
= 4.33 × 10<sup>-5</sup> mol L<sup>-1</sup>S<sup>-1</sup></p>
<p>Rate of disappearance of A<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72362" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-33.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 33" width="168" height="53" /><br />
2/3 × 1.3 × 10<sup>-4</sup> L<sup>-1</sup>S<sup>-1</sup><br />
= 8.66 × 10<sup>-5</sup> mol L<sup>-1</sup>S<sup>-1</sup></p>
<p>Question 6.<br />
The rate law for a reaction is found to be<br />
Rate = K [NO<sup>&#8211;</sup><sub>2</sub>] [I<sup>&#8211;</sup> ] [H<sup>+</sup>]<sup>2</sup> How would the rate of reaction change when<br />
(i) Concentration of H<sup>+</sup> is doubled<br />
(ii) Concentration of I<sup>&#8211;</sup> is halved<br />
(iii) Concentration of each of NO<sub>2</sub>, I<sup>&#8211;</sup> and H<sup>+</sup> are tripled ?<br />
Answer:<br />
Suppose initially the concentration are [NO<sup>&#8211;</sup><sub>2</sub>] = a mol L<sup>-1</sup>, [I<sup>&#8211;</sup> ] = b mol L<sup>&#8211;</sup> and [H<sup>+</sup>] = c mol L<sup>-1</sup><br />
∴ Rate = K abc2</p>
<p>(i) New [H<sup>+</sup>] = 2c<br />
∴ New rate = 4ab (2c)<sup>2</sup> = 4abc2<br />
= 4 times</p>
<p>(ii) New [I<sup>&#8211;</sup> ] = \(\frac { b }{ 2 }\)<br />
New Rate = Ka\(\frac { b }{ 2 }\)c<sup>2</sup>= \(\frac { 1 }{ 2 }\) Kabc<sup>2</sup><br />
ie. rate of reaction is halved</p>
<p>(iii) New [NO<sup>&#8211;</sup><sub>2</sub>] = 3a, [I<sup>&#8211;</sup> ] = 3b, [H<sup>+</sup>] = 3c<br />
New rate = K (3a) (3b) (3c)<sup>2</sup><br />
= 81K abc<sup>2</sup> = 81 times.</p>
<p>Question 7.<br />
The decomposition of NH<sub>3</sub> on platinum surface<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72365" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-34.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 34" width="276" height="30" /><br />
is zero order with k = 2.5 × 10<sup>-4</sup> mol L<sup>-1</sup> S<sup>-1</sup><br />
What are the rates of production of N<sub>2</sub> and H<sub>2</sub><br />
Answer:<br />
2NH<sub>3</sub> -&gt; N<sub>2</sub> + 3H<sub>2</sub><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72366" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-35.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 35" width="345" height="58" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-35.png 345w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-35-300x50.png 300w" sizes="auto, (max-width: 345px) 100vw, 345px" /><br />
For zero order reaction, rate = K<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72367" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-36.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 36" width="258" height="63" /><br />
= 2.5 × 10<sup>-4</sup> mol L<sup>-1</sup> S<sup>-1</sup><br />
Rate of production of H<sub>2</sub> = \(\frac{\mathrm{d}\left[\mathrm{H}_{2}\right]}{\mathrm{dt}}\)<br />
= 3 × (2.5 × 10<sup>-4</sup> mol L<sup>-1</sup> S<sup>-1</sup>)<br />
= 7.5 × 10<sup>-4</sup> mol <sup>-1</sup> S<sup>-1</sup></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 8.<br />
Why does coal not burn by itself in air, but once initiated by a flame, continues to bum ?<br />
Answer:<br />
Activation energy for the combustion reaction is very high and is not available at room temperature. Oh applying flame, to a part of the coal and air in contact with the flame absorb heat which provides the necessary activation energy and combustion starts. The heat liberated further provides activation energy for the combustion to continue.</p>
<p>Question 9.<br />
Following reaction takes place in one step:<br />
2NO(g) + O<sub>2</sub>(g) ⇌ 2NO<sub>2</sub>(g)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72368" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-37.png" alt="2nd PUC Chemistry Question Bank Chapter 4 Chemical Kinetics - 37" width="351" height="304" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-37.png 351w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-4-Chemical-Kinetics-37-300x260.png 300w" sizes="auto, (max-width: 351px) 100vw, 351px" /><br />
\(\frac{\mathbf{r}_{2}}{\mathbf{r}_{1}}\) = 27 or r<sub>2</sub> = 27r<sub>1</sub> ie rate becomes 27<br />
times<br />
There is no effect on the order of reaction.</p>
<p>Question 10.<br />
Rate constant K of a reaction varies with temperature according to the equation<br />
log K = constant . \(\frac{\mathbf{E} \mathbf{a}}{2.303 \mathbf{R}} \frac{\mathbf{1}}{\mathbf{T}}\)<br />
Answer:<br />
where E<sub>a</sub> is the energy of activation for the reaction. When a graph is plotted for<br />
log K versus\(\frac { 1 }{ T }\), a straight line with a slope 6670 K is obtained. Calculate the energy of activation for this reaction. State units (R = 8.314JK<sup>-1</sup> mol<sup>-1</sup>)<br />
Answer:<br />
Slope of the lin,e<br />
\(\frac{-E a}{2.303 R}\) =-6670K<br />
Ea = 2.303 × 8.314 (JK<sup>-1</sup> mol<sup>-1</sup>) × 6670K<br />
= 127711.4J mol<sup>-1</sup>.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
</div>
</div>
</div>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10244</post-id>	</item>
		<item>
		<title>2nd PUC Chemistry Question Bank Chapter 13 Amines</title>
		<link>https://ktbssolutions.com/2nd-puc-chemistry-question-bank-chapter-13/</link>
		
		<dc:creator><![CDATA[Prasanna]]></dc:creator>
		<pubDate>Tue, 14 Jul 2026 09:32:53 +0000</pubDate>
				<category><![CDATA[2nd PUC]]></category>
		<guid isPermaLink="false">https://ktbssolutions.com/?p=10253</guid>

					<description><![CDATA[You can Download Chapter 13 Amines Questions and Answers, Notes, 2nd PUC Chemistry Question Bank with Answers Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations. Karnataka 2nd PUC Chemistry Question Bank Chapter 13 Amines 2nd PUC Chemistry Amines NCERT Textbook Questions Question 1. Write IUPAC names [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>You can Download Chapter 13 Amines Questions and Answers, Notes, <a href="https://ktbssolutions.com/2nd-puc-chemistry-question-bank/">2nd PUC Chemistry Question Bank with Answers</a> Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations.</p>
<h2>Karnataka 2nd PUC Chemistry Question Bank Chapter 13 Amines</h2>
<h3>2nd PUC Chemistry Amines NCERT Textbook Questions</h3>
<p>Question 1.<br />
Write IUPAC names of the following compounds and classify them into primary, secondary .and tertiary amines.<br />
(i) (CH<sub>3</sub>)<sub>2</sub>CHNH<sub>2</sub><br />
(ii) CH<sub>3</sub>(CH<sub>2</sub>)<sub>2</sub>NH<br />
(iii) CH<sub>3</sub>NHCH(CH<sub>3</sub>)<sub>2</sub><br />
(iv) (CH<sub>3</sub>)<sub>3</sub>CNH<sub>2</sub><br />
(V) C<sub>6</sub>H<sub>5</sub>NHCH<sub>3</sub><br />
(vi) (CH<sub>3</sub>CH<sub>2</sub>)<sub>2</sub>NCH<sub>3</sub><br />
(vii) m-BrC<sub>6</sub>H<sub>4</sub>NH<sub>2</sub><br />
Answer:</p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72847" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-1.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 1" width="716" height="552" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-1.png 716w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-1-300x231.png 300w" sizes="auto, (max-width: 716px) 100vw, 716px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 2.<br />
Give one chemical test to distinguish between the following pairs of compounds,</p>
<ol>
<li>Methylamine and dimethylamine</li>
<li>Secondary and tertiary amines</li>
<li>Ethylamine and aniline</li>
<li>Aniline and benzylamine</li>
<li>Aniline and N-methyl aniline.</li>
</ol>
<p>Answer:<br />
1. Methylamine and dimethylamine<br />
(1) CH<sub>3</sub>NH<sub>2</sub> (Methyl amine; 1° amine) &#8211; Carbyl amine test positive<br />
(2) (CH<sub>3</sub>)<sub>2</sub> NH (Dimethyl amine; 2° amine) &#8211; Doesn’t give this test<br />
Carbylamine test:-<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72855" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-2.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 2" width="566" height="93" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-2.png 566w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-2-300x49.png 300w" sizes="auto, (max-width: 566px) 100vw, 566px" /></p>
<p>2. 2° and 3° amines:-<br />
(1) 2° amine &#8211; Libermann Nitrosomine test positive<br />
(2) 3° amine &#8211; Libermann Nitrosomine test negative.<br />
Libermann Nitrosomine test :<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72858" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-3.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 3" width="460" height="133" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-3.png 460w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-3-300x87.png 300w" sizes="auto, (max-width: 460px) 100vw, 460px" /></p>
<p>3. Ethylamine and aniline:<br />
(1) Aromatic amines gives brilliantly coloured orange dye on diazotisation and coupling with phenol.<br />
(2) Ethylamine do not give a dye on diazotisation and coupling with phenol.<br />
Diazotisation:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72861" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-4.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 4" width="473" height="255" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-4.png 473w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-4-300x162.png 300w" sizes="auto, (max-width: 473px) 100vw, 473px" /></p>
<p>4. Aniline and benzylamine:-<br />
(1) Aromatic (1 °) amine gives coloured dye on diazotisation and coupling with phenol.<br />
(2) Other non aromatic 1° amines and which are not an aromatic 1° amine, will not give a dye.<br />
Diazotisation:-<br />
(a)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72865" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-5.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 5" width="474" height="226" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-5.png 474w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-5-300x143.png 300w" sizes="auto, (max-width: 474px) 100vw, 474px" /></p>
<p>(b)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72870" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-6.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 6" width="556" height="33" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-6.png 556w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-6-300x18.png 300w" sizes="auto, (max-width: 556px) 100vw, 556px" /></p>
<p>5. Aniline and N-methylaniline:-<br />
aniline (1° amine)-Carbylamine test positive<br />
N-methylaniline (2° amine) &#8211; Negative<br />
Carbylamine test:-<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72874" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-7.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 7" width="663" height="230" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-7.png 663w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-7-300x104.png 300w" sizes="auto, (max-width: 663px) 100vw, 663px" /></p>
<p>Question 3.<br />
Account for the following:</p>
<p>1. pK<sub>b</sub> of aniline is more than that of methylamine.<br />
Answer:<br />
(i) Aniline is weaker base than methylamine<br />
K<sub>b</sub> of aniline is less than K<sub>b</sub> of methylamine.<br />
pK<sub>b</sub> of aniline is more than pK<sub>b</sub> of methylamine.<br />
PK<sub>b</sub> = -logK<sub>b</sub><br />
(a) Aniline is weaker base than methylamine because due to resonance, lone pair on N<sub>2</sub> gets delocalised over the ring, so electron pair availability is reduced.</p>
<p>(b) In methyl amine due to &#8216;+I&#8217;effect of methyl group, availability of lone pair on N<sub>2</sub> atom is increased So is strong base.</p>
<p>2. Ethylamine is soluble in water whereas aniline is not.<br />
Answer:<br />
(i) Lower aliphatic amines are soluble in water because of their ability to form hydrogen bonds with water.<br />
(ii) But in aniline due to larger hydrocarbon part, it hinders hydrogen bond formation with water.</p>
<p>3. Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.<br />
Answer:<br />
Methylamine + H<sub>2</sub>O ⇌ Methyl ammonium hydroxide<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72879" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-8.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 8" width="402" height="54" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-8.png 402w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-8-300x40.png 300w" sizes="auto, (max-width: 402px) 100vw, 402px" /><br />
OH- can precipitate out Fe, AI, Cr etc&#8230;<br />
3 [CH<sub>3</sub>NH<sub>3</sub>]<sup>+</sup> OH + FeCl<sub>3</sub> → Fe (OH)<sub>3</sub>↓+ 3CH<sub>3</sub>NH<sub>3</sub>Cl<br />
Fe (OH)<sub>3</sub> is unstable, so can be hydrated ferric oxide<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72887" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-9.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 9" width="341" height="48" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-9.png 341w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-9-300x42.png 300w" sizes="auto, (max-width: 341px) 100vw, 341px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>4. Although amino group is o- and p- directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.<br />
Answer:<br />
In aniline NH<sub>2</sub> increases e density at o- and p- positions due to +R effect. But when it is nitrated by nitrating mixture, substantial amount of m-nitro aniline is formed.<br />
But in acidic medium (Nitrating mixture &#8211; HNO<sub>3</sub> (c) + H<sub>2</sub>SO<sub>4</sub> (c)).<br />
NH<sub>2</sub> + H<sup>+</sup> ⇌ NH<sub>3</sub><sup>+</sup>, NH<sub>3</sub><sup>+</sup> is e<sup>&#8211;</sup> withdrawing group and so is m &#8211; directing. So gives larger amount of m- nitroaniline.</p>
<p>5. Aniline does not undergo Friedel-Crafts reaction.<br />
Answer:<br />
Friedel-Craft reaction:-<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72894" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-10.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 10" width="515" height="298" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-10.png 515w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-10-300x174.png 300w" sizes="auto, (max-width: 515px) 100vw, 515px" /><br />
But aniline undergoes salt formation with A1C13 (Lewis acid used as catalyst). So N acquires positive charge and hence acts as strong deactivating group for further reaction.</p>
<p>6. Diazonium salts of aromatic amines are more stable than those of aliphatic amines.<br />
Answer:<br />
In aromatic diazonium salts, due to resonance their is dispersal of positive charge on benzene ring.<br />
But in aliphatic diazonium salts, resonance is not possible, so aliphatic diazonium salts are less stable than aromatic diazonium salts.</p>
<p>7. Gabriel phthalimide synthesis is preferred for synthesising primary amines.<br />
Answer:<br />
Gabriel phthalimide synthesis<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72896" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 11" width="647" height="285" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11.png 647w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11-300x132.png 300w" sizes="auto, (max-width: 647px) 100vw, 647px" /><br />
Reaction between alkyl halide (R &#8211; X) and ammonia gives mixture, of 1°, 2° and 3° amines with tetraalkyl ammonium halide. Mixture is not separable.<br />
To get pure 1° amine, Gabriel phthalimide synthesis is preferred.</p>
<p>Question 4.<br />
Arrange the following:<br />
1. In decreasing order of the pKb values:<br />
C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>, C<sub>6</sub>H<sub>5</sub>NHCH<sub>3</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH and CH<sub>5</sub>NH<sub>2</sub><br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &gt; C<sub>6</sub>H<sub>5</sub>NHCH<sub>3</sub> &gt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &gt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> NH<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72898" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-12.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 12" width="445" height="108" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-12.png 445w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-12-300x73.png 300w" sizes="auto, (max-width: 445px) 100vw, 445px" /></p>
<p>2. In increasing order of basic strength:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, C<sub>6</sub>H<sub>5</sub>N(CH<sub>3</sub>)<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH and CH<sub>3</sub>NH<sub>2</sub><br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>6</sub>H<sub>5</sub>N(CH<sub>3</sub>)<sub>2</sub> &lt; CH<sub>3</sub>NH<sub>2</sub> &lt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> NH</p>
<p>3. In increasing order of basic strength:<br />
(a) Aniline, p-nitroaniline and p-toluidine<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72900" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-13.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 13" width="396" height="102" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-13.png 396w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-13-300x77.png 300w" sizes="auto, (max-width: 396px) 100vw, 396px" /></p>
<p>(b) C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, C<sub>6</sub>H<sub>5</sub>NHCH<sub>3</sub>, C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>.<br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>6</sub>H<sub>5</sub>NHCH<sub>3</sub> &lt; C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub></p>
<p>4. In decreasing order of basic strength in gas phase:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH, (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N and NH<sub>3</sub>,<br />
Answer:<br />
(C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N &gt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH &gt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &gt; NH<sub>3</sub><br />
Note: In GAS PHASE, 3° &gt; 2° &gt; 1° Ammonia [No Hydrogen bending and ‘+I&#8217; effect].</p>
<p>5. In increasing order of boiling point:<br />
C<sub>2</sub>H<sub>5</sub>OH, (CH<sub>3</sub>)<sub>2</sub>NH, C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub><br />
Answer:<br />
(CH<sub>3</sub>)<sub>2</sub> NH &lt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>2</sub>H<sub>5</sub>OH<br />
Note: Stronger H-bonding, more b.p more solubility<br />
Alcohol &gt; Amine In amines on H attached to N takes part in H-bond.</p>
<p>6. In increasing order of solubility in water:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH, C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>.<br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH &lt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub><br />
more H-bonding, more solubility</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 5.<br />
How will you convert:<br />
1. Ethanoic acid into methanamine<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72902" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-14.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 14" width="668" height="146" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-14.png 668w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-14-300x66.png 300w" sizes="auto, (max-width: 668px) 100vw, 668px" /></p>
<p>2. Hexanenitrile into 1-aminopentane<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72903" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-15.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 15" width="652" height="52" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-15.png 652w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-15-300x24.png 300w" sizes="auto, (max-width: 652px) 100vw, 652px" /></p>
<p>3. Methonal to ethanoic acid<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72905" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-16.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 16" width="548" height="33" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-16.png 548w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-16-300x18.png 300w" sizes="auto, (max-width: 548px) 100vw, 548px" /></p>
<p>4. Ethanamine into methanamine<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72906" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-17.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 17" width="634" height="122" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-17.png 634w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-17-300x58.png 300w" sizes="auto, (max-width: 634px) 100vw, 634px" /></p>
<p>5. Ethanoic acid into propanoic acid<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72908" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-18.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 18" width="597" height="114" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-18.png 597w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-18-300x57.png 300w" sizes="auto, (max-width: 597px) 100vw, 597px" /></p>
<p>6. Methanamine into ethanamine<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72909" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-19.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 19" width="474" height="82" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-19.png 474w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-19-300x52.png 300w" sizes="auto, (max-width: 474px) 100vw, 474px" /></p>
<p>7. Nitromethane into dimethylamine<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72911" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-20.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 20" width="596" height="65" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-20.png 596w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-20-300x33.png 300w" sizes="auto, (max-width: 596px) 100vw, 596px" /></p>
<p>8. Propanoic acid into ethanoic acid<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72913" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-21.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 21" width="519" height="116" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-21.png 519w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-21-300x67.png 300w" sizes="auto, (max-width: 519px) 100vw, 519px" /></p>
<p>Question 6.<br />
Describe a method for the identification of primary, secondary and tertiary amines. Also write chemical equations of the reactions involved.<br />
Answer:<br />
Hinsberg test:- Benzenesulphonyl chloride (C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl), which is also known as Hinsberg’s reagent, reacts with primary and secondary amines to form sulphonamides.<br />
(a) The reaction of benzenesulphonyl chloride with primary amine yields N-ethylbenzenesulphonyl amide.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72915" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-22.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 22" width="522" height="140" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-22.png 522w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-22-300x80.png 300w" sizes="auto, (max-width: 522px) 100vw, 522px" /><br />
The hydrogen attached to nitrogen in sulphonamide is strongly acidic due to the presence of strong electron withdrawing sulphonyl group. Hence, it is soluble in alkali.</p>
<p>(b) In the reaction with secondary amine, N,N-diethylbenzenesulphonamide is formed.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72917" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-23.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 23" width="524" height="127" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-23.png 524w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-23-300x73.png 300w" sizes="auto, (max-width: 524px) 100vw, 524px" /><br />
Since N, N-diethylbenzene sulphonamide does not contain any hydrogen atom attached to nitrogen atom, it is not acidic and hence insoluble in alkali.</p>
<p>(c) Tertiary amines do not react with benzenesulphonyl chloride. This property of amines reacting with benzenesulphonyl chloride, in a different manner is used for the distinction of primary, secondary and tertiary amines and also for the separation of a mixture of amines. However, these days benzenesulphonyl chloride is replaced by p-toluenesulphonyl chloride.<br />
1° amine &#8211; clear solution which on acidification gives insoluble product.<br />
2° amine &#8211; insoluble product in solution, unaffected by acid<br />
3° amine &#8211; No reaction, dissolves an acidification.</p>
<p><strong><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></strong></p>
<p>Question 7.<br />
Write short notes on the following:</p>
<ol>
<li> Carbylamine reaction</li>
<li>Diazotisation</li>
<li>Hofmann’s bromamide reaction</li>
<li>Coupling reaction</li>
<li>Ammonolysis</li>
<li>Acetylation</li>
<li>Gabriel phthalimide synthesis.</li>
</ol>
<p>Answer:<br />
1. Carbylamine reaction<br />
1° amines (aromatic/aliphatic) On heating with chloroform and alcoholic solution of KOH gives isocyanides/carbylamines producing unpleasant smell.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72918" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 24" width="548" height="80" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24.png 548w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24-300x44.png 300w" sizes="auto, (max-width: 548px) 100vw, 548px" /><br />
2° and 3° (aromatic/aliphatic) do not give this reaction.</p>
<p>2. Diazotisation .<br />
Aromatic 1° amines into diazonium salts by action of HNO<sub>2</sub> and dil HCl at ice cold temperature as HNO<sub>2</sub> and product are unstable at higher temperature.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72921" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 25" width="457" height="107" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25.png 457w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25-300x70.png 300w" sizes="auto, (max-width: 457px) 100vw, 457px" /><br />
3. Hofmann’s bromamide reaction<br />
Involves heating of an amide with bromine and caustic alkali to yield an amine with one carbon less than original amide.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72925" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 26" width="496" height="56" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26.png 496w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26-300x34.png 300w" sizes="auto, (max-width: 496px) 100vw, 496px" /><br />
4. Coupling reaction<br />
Diazonium salt acts as electrophile and brings about substitution in electron rich aromatic ring such as phenol and amines. The result is formation of dye.<br />
(i) with phenol &#8211; In basic medium (9 &#8211; 10 pH) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72926" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 27" width="649" height="119" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27.png 649w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27-300x55.png 300w" sizes="auto, (max-width: 649px) 100vw, 649px" /></p>
<p>(ii) with amines &#8211; In acidic medium (ph = 4 &#8211; 5) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72927" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 28" width="630" height="81" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28.png 630w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28-300x39.png 300w" sizes="auto, (max-width: 630px) 100vw, 630px" /></p>
<p>5. Ammonolysis &#8211; Alkyl halide (1°) react with alcoholic ammonia to form 1°, 2°, 3° amines along with 4°ammonium salts. It is carried out by heating alkyl halide with ale solution of NH3 in sealed tube at 370 K.<br />
If ammonia is used in excess, 1° amine is major product<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72928" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-29.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 29" width="279" height="53" /><br />
If alkyl halide is excess, it forms all 1°, 2°, 3°, 4° ammonium salts<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72930" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 30" width="322" height="96" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30.png 322w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30-300x89.png 300w" sizes="auto, (max-width: 322px) 100vw, 322px" /></p>
<p>6. Acetylation<br />
Aliphatic amines:<br />
Introduction of acetyl group (CH<sub>3</sub>CO-) into any molecule.<br />
1° and 2° amines react with acetyl chloride to form amides<br />
But 3° amines has NO H on N, so do not react.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72932" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 31" width="676" height="350" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31.png 676w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31-300x155.png 300w" sizes="auto, (max-width: 676px) 100vw, 676px" /><br />
7. Gabriel phthalimide synthesis<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72934" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 11(i)" width="647" height="285" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11i.png 647w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11i-300x132.png 300w" sizes="auto, (max-width: 647px) 100vw, 647px" /><br />
Reaction between alkyl halide (R &#8211; X) and ammonia gives mixture, of 1°, 2° and 3° amines with tetraalkyl ammonium halide. Mixture is not separable.<br />
To get pure 1° amine, Gabriel phthalimide synthesis is preferred.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 8.<br />
Accomplish the following conversions:</p>
<ol>
<li>Nitrobenzene to benzoic acid</li>
<li>Benzene to m-bromophenol</li>
<li>Benzoic acid to aniline</li>
<li>Aniline to 2,4,6-tribromofluorobenzene</li>
<li>Benzyl chloride to 2-phenylethanamine</li>
<li>Chlorobenzene to p-chloroaniline</li>
<li>Aniline to p-bromoaniline</li>
<li>Benzamide to toluene</li>
<li>Aniline to benzyl alcohol</li>
</ol>
<p>Answer:<br />
1. Nitrobenzene to benzoic acid<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72936" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-32.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 32" width="610" height="203" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-32.png 610w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-32-300x100.png 300w" sizes="auto, (max-width: 610px) 100vw, 610px" /></p>
<p>2. Benezene to m-bromophenol<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72938" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-33.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 33" width="635" height="257" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-33.png 635w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-33-300x121.png 300w" sizes="auto, (max-width: 635px) 100vw, 635px" /></p>
<p>3. Benzoic acid to aniline<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72940" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-34.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 34" width="357" height="105" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-34.png 357w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-34-300x88.png 300w" sizes="auto, (max-width: 357px) 100vw, 357px" /></p>
<p>4. Aniline to 2,4,6-tribromofluorobenzene<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72941" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-35.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 35" width="540" height="137" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-35.png 540w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-35-300x76.png 300w" sizes="auto, (max-width: 540px) 100vw, 540px" /></p>
<p>5. Benzyl chloride to 2-phenylethanamine<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72942" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-36.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 36" width="500" height="123" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-36.png 500w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-36-300x74.png 300w" sizes="auto, (max-width: 500px) 100vw, 500px" /></p>
<p>6. Chlorobenzene to p-choloroaniline</p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72944" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-38.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 38" width="472" height="162" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-38.png 472w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-38-300x103.png 300w" sizes="auto, (max-width: 472px) 100vw, 472px" /></p>
<p>7. Aniline to p-bromoaniline<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72946" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-39.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 39" width="508" height="300" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-39.png 508w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-39-300x177.png 300w" sizes="auto, (max-width: 508px) 100vw, 508px" /></p>
<p>8. Benzeamide to toluene</p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72948" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-40.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 40" width="665" height="132" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-40.png 665w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-40-300x60.png 300w" sizes="auto, (max-width: 665px) 100vw, 665px" /></p>
<p>9. Aniline to benzeyl alcohal<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72950" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-41.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 41" width="680" height="157" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-41.png 680w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-41-300x69.png 300w" sizes="auto, (max-width: 680px) 100vw, 680px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 9.<br />
Give the structures of A,B and C in the following reactions:</p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72953" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-89.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 89" width="447" height="31" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-89.png 447w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-89-300x21.png 300w" sizes="auto, (max-width: 447px) 100vw, 447px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72952" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-90.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 90" width="473" height="142" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-90.png 473w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-90-300x90.png 300w" sizes="auto, (max-width: 473px) 100vw, 473px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72955" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-91.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 91" width="410" height="37" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-91.png 410w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-91-300x27.png 300w" sizes="auto, (max-width: 410px) 100vw, 410px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72956" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-92.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 92" width="497" height="125" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-92.png 497w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-92-300x75.png 300w" sizes="auto, (max-width: 497px) 100vw, 497px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72959" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-93.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 93" width="435" height="37" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-93.png 435w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-93-300x26.png 300w" sizes="auto, (max-width: 435px) 100vw, 435px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72961" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-94.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 94" width="477" height="171" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-94.png 477w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-94-300x108.png 300w" sizes="auto, (max-width: 477px) 100vw, 477px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72963" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-95.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 95" width="460" height="37" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-95.png 460w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-95-300x24.png 300w" sizes="auto, (max-width: 460px) 100vw, 460px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72965" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-96.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 96" width="590" height="63" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-96.png 590w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-96-300x32.png 300w" sizes="auto, (max-width: 590px) 100vw, 590px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72967" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-97.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 97" width="433" height="36" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-97.png 433w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-97-300x25.png 300w" sizes="auto, (max-width: 433px) 100vw, 433px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72968" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-98.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 98" width="633" height="63" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-98.png 633w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-98-300x30.png 300w" sizes="auto, (max-width: 633px) 100vw, 633px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72969" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-99.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 99" width="424" height="42" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-99.png 424w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-99-300x30.png 300w" sizes="auto, (max-width: 424px) 100vw, 424px" /><br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72970" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-100.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 100" width="571" height="217" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-100.png 571w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-100-300x114.png 300w" sizes="auto, (max-width: 571px) 100vw, 571px" /><br />
Question 10.<br />
An aromatic compound ‘A’ on treatment with aqueous ammonia and heating forms compound ‘B’ which on heating with Br2 and KOH forms a compound ‘C’ of molecular formula C<sub>6</sub>H<sub>7</sub>N. Write the structures and IUPAC names of compounds A, B and C.<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72972" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-44.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 44" width="265" height="75" /><br />
As ‘C’ is expected as a 1° amine obtained by Hoffmann bromamide degradation of ‘B’ an amide obtained from ‘A’ a carboxylic acid on treatment with NH<sub>3</sub> and heat.<br />
So<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72974" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-45.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 45" width="518" height="161" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-45.png 518w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-45-300x93.png 300w" sizes="auto, (max-width: 518px) 100vw, 518px" /></p>
<p>Question 11.<br />
Complete the following reactions:<br />
1. C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + CHCI<sub>3</sub> + alc.KOH →<br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + CHCl<sub>3</sub> + alc.KOH → C<sub>6</sub>H<sub>5</sub>NC + 3 KCl + 3H<sub>2</sub>O<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72977" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-46.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 46" width="610" height="105" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-46.png 610w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-46-300x52.png 300w" sizes="auto, (max-width: 610px) 100vw, 610px" /></p>
<p>2. C<sub>6</sub>H<sub>5</sub>N<sub>2</sub>Cl + H<sub>3</sub>PO<sub>2</sub> + H<sub>2</sub>O →<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72978" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-47.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 47" width="569" height="83" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-47.png 569w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-47-300x44.png 300w" sizes="auto, (max-width: 569px) 100vw, 569px" /></p>
<p>3. C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + H<sub>2</sub>SO<sub>4</sub> (conc.) →<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72981" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-48.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 48" width="479" height="280" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-48.png 479w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-48-300x175.png 300w" sizes="auto, (max-width: 479px) 100vw, 479px" /></p>
<p>4. C<sub>6</sub>H<sub>5</sub>N<sub>2</sub>Cl + C<sub>2</sub>H<sub>5</sub>OH →<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72983" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-49.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 49" width="460" height="85" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-49.png 460w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-49-300x55.png 300w" sizes="auto, (max-width: 460px) 100vw, 460px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>5. C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + Br<sub>2</sub>(aq) →<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72985" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-50.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 50" width="489" height="138" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-50.png 489w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-50-300x85.png 300w" sizes="auto, (max-width: 489px) 100vw, 489px" /></p>
<p>6. C<sub>6</sub>H<sub>5</sub>N<sub>2</sub> + (CH<sub>3</sub>CO)<sub>2</sub> →<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72986" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-51.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 51" width="557" height="118" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-51.png 557w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-51-300x64.png 300w" sizes="auto, (max-width: 557px) 100vw, 557px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-72988" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-52.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 52" width="703" height="154" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-52.png 703w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-52-300x66.png 300w" sizes="auto, (max-width: 703px) 100vw, 703px" /></p>
<p>Question 12.<br />
Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?<br />
Answer:<br />
In this reaction, potassium phthalimide gives phthalimide anion which acts as nucleophile and attacks electrophilic carbon of alkyl halide.</p>
<p>But due to much less reactivity of aryl halide (nucleophilic substitution reaction), 1° aromatic amines can’t be prepared.</p>
<p>Question 13.<br />
Write the reactions of<br />
1. aromatic and<br />
2. aliphatic primary amines with nitrous acid.<br />
Answer:<br />
1. Aromatic amines with nitrous acid<br />
Aromatic 1° amines react with HNO<sub>2</sub> at 273 &#8211; 278 K to form diazonium compound.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72990" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-53.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 53" width="480" height="114" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-53.png 480w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-53-300x71.png 300w" sizes="auto, (max-width: 480px) 100vw, 480px" /></p>
<p>2. Aliphatic amines with HNO<sub>2</sub> at 273 &#8211; 278 K to give corresponding alcohol, N<sub>2</sub>, along with other products.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72991" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-54.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 54" width="417" height="85" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-54.png 417w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-54-300x61.png 300w" sizes="auto, (max-width: 417px) 100vw, 417px" /></p>
<p>Question 14.<br />
Give plausible explanation for each of the following:<br />
1. Why are amines less acidic than alcohols of comparable molecular masses?<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72992" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-55.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 55" width="468" height="166" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-55.png 468w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-55-300x106.png 300w" sizes="auto, (max-width: 468px) 100vw, 468px" /><br />
But as ‘O’ is more electronegative than ‘N’. So ‘O’ can accommodate more positive charge and is more stable than ‘N’. So alcohol liberates H+ easily than amines.<br />
So alcohols are more acidic than amines.</p>
<p>2. Why do primary amines have higher boiling point than tertiary amines?<br />
Answer: 1° amines (NH2) has stronger and extensive H &#8211; bonding.<br />
3° amines (&gt; N-) has no H, so no H &#8211; bonding.<br />
So 1° amines have higher b.p than 3° amines.</p>
<p>3. Why are aliphatic amines stronger bases than aromatic amines?<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72994" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-56.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 56" width="497" height="54" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-56.png 497w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-56-300x33.png 300w" sizes="auto, (max-width: 497px) 100vw, 497px" /><br />
Alkyl amines has positive I effect/electron donating effect, so high electron density on N and stable alkyl ammonium ion formation.<br />
Aromatic amines due to resonance effect and lower stability of aryl ammonium ion than aryl amine, e- density on N is less.<br />
So Alkyl amine is stronger base than aromatic amines.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<h3>2nd PUC Amines Intext Questions</h3>
<p>Question 15.<br />
Classify as primary, secondary or tertiary amines.<br />
1.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72996" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-57.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 57" width="117" height="98" /><br />
2.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72997" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-58.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 58" width="143" height="99" /></p>
<p>3. (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> CHNH<sub>2</sub><br />
4. (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> NH<br />
Answer:<br />
1.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72998" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-59.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 59" width="124" height="117" /><br />
→ Primary(As only one of H is replaced by other group, contains &#8211; NH<sub>2</sub> group)</p>
<p>2.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72999" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-60.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 60" width="141" height="115" /><br />
→ No H attached to N, so teritary ( As, &gt; N group is teritary)</p>
<p>3. (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> CHNH<sub>2</sub> —&gt; Primary (contains &#8211; NH<sub>2</sub> group)<br />
4. (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH —&gt; Secondary (contains -NH group)</p>
<p>Question 16.<br />
(i) Write a structure of different isomeric amines corresponding to C<sub>4</sub>H<sub>11</sub>N<br />
(ii) Write IUPAC names of all isomers<br />
(iii) What type of isomerism is exhibited by different pair of amines<br />
Answer:<br />
C<sub>5</sub>H<sub>11</sub>N<br />
Primary amines (-NH<sub>2</sub>)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73000" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-61.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 61" width="558" height="161" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-61.png 558w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-61-300x87.png 300w" sizes="auto, (max-width: 558px) 100vw, 558px" /><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73001" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-62.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 62" width="735" height="514" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-62.png 735w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-62-300x210.png 300w" sizes="auto, (max-width: 735px) 100vw, 735px" /></p>
<p>Question 17.<br />
Convert:<br />
(a) Benzene into aniline<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73004" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-63.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 63" width="469" height="126" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-63.png 469w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-63-300x81.png 300w" sizes="auto, (max-width: 469px) 100vw, 469px" /></p>
<p>(b) Benzene into N,N &#8211; dimethyl aniline<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73005" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-64.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 64" width="685" height="129" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-64.png 685w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-64-300x56.png 300w" sizes="auto, (max-width: 685px) 100vw, 685px" /></p>
<p>(c) Cl &#8211; [CH<sub>2</sub>]<sub>4</sub> &#8211; Cl into hexane-1,6 &#8211; diamine<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73006" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-65.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 65" width="508" height="95" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-65.png 508w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-65-300x56.png 300w" sizes="auto, (max-width: 508px) 100vw, 508px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 18.<br />
Arrange following in increasing order of their Basic character:<br />
1. C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>, C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, NH<sub>3</sub>, C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub><br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; NH<sub>3</sub> &lt; C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub> &lt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &lt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH</p>
<p>2. C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)NH, (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N, C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub><br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>2</sub>H<sub>5</sub>)<sub>3</sub><sub>N</sub> &lt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH</p>
<p>3. CH<sub>3</sub>NH<sub>2</sub>, (CH<sub>3</sub>)<sub>2</sub>NH, (CH<sub>3</sub>)<sub>3</sub>N, C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>, C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2<br />
</sub><br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> &lt; C<sub>2</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub> &lt; (CH<sub>3</sub>)<sub>3</sub>N &lt; CH<sub>3</sub>NH<sub>2</sub> &lt; (CH<sub>3</sub>)<sub>2</sub>NH<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73008" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-66.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 66" width="666" height="175" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-66.png 666w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-66-300x79.png 300w" sizes="auto, (max-width: 666px) 100vw, 666px" /></p>
<p>Question 19.<br />
Compliete following acid-base reaction and name the products:<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73011" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-67.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 67" width="547" height="111" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-67.png 547w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-67-300x61.png 300w" sizes="auto, (max-width: 547px) 100vw, 547px" /></p>
<p>Question 20.<br />
Write reactions of final alkylation product of aniline with excess of methyl iodine is presence of solution<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73014" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-68.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 68" width="645" height="683" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-68.png 645w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-68-283x300.png 283w" sizes="auto, (max-width: 645px) 100vw, 645px" /></p>
<p>Question 21.<br />
Write chemical reaction of aniline with benzoyl chloride and write product name.<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73018" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-69.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 69" width="558" height="146" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-69.png 558w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-69-300x78.png 300w" sizes="auto, (max-width: 558px) 100vw, 558px" /></p>
<p>Question 22.<br />
Write structure of isomers of C<sub>3</sub>H<sub>9</sub>N. Write IUPAC names of isomers which will liberate N<sub>2</sub> gas on treatment with nitrous acid. .<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73020" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-70.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 70" width="582" height="330" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-70.png 582w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-70-300x170.png 300w" sizes="auto, (max-width: 582px) 100vw, 582px" /></p>
<p>Question 23.<br />
Convert<br />
1. 3-methylaniline into 3-nitrotolune<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73026" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-71.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 71" width="638" height="146" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-71.png 638w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-71-300x69.png 300w" sizes="auto, (max-width: 638px) 100vw, 638px" /></p>
<p>2. Aniline into 1,3,5 &#8211; tribromobenzene<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73030" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-72.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 72" width="677" height="181" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-72.png 677w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-72-300x80.png 300w" sizes="auto, (max-width: 677px) 100vw, 677px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<h3>2nd PUC Amines Additional Questions</h3>
<p>Question 1.<br />
Complete the reaction.<br />
C<sub>6</sub>H<sub>5</sub>N<sub>2</sub>Cl + CH<sub>3</sub>CH<sub>2</sub>OH → (Benzene)<br />
Answer:<br />
C<sub>6</sub>H<sub>5</sub>N<sub>2</sub>Cl + CH<sub>3</sub>CH<sub>2</sub>OH → C<sub>6</sub>H<sub>6</sub> +CH<sub>3</sub>CHO + N<sub>2</sub> + HCl</p>
<p>Question 2.<br />
Write the IUPAC name of C<sub>6</sub>H<sub>6</sub>NHCH<sub>3</sub> .<br />
Answer:<br />
N &#8211; Methyl aniline.</p>
<p>Question 3.<br />
Which is more soluble in water, NH<sub>3</sub> or methylamine ?<br />
Answer:<br />
NH<sub>3</sub> is more soluble in water due to more H-bonding.</p>
<p>Question 4.<br />
Which of the following amines has largest value of pK<sub>b</sub>?<br />
p-Toluidine, Aniline, p- Nitroaniline.<br />
Answer:<br />
Higher the pK<sub>b</sub> value, weaker is the base<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73034" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-73.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 73" width="296" height="170" /><br />
Presence of -CH<sub>3</sub> group in the ring will increase the basic character as it is an electron releasing group. Presence of -NO<sub>2</sub> group in the ring will decrease the basic character as it an electron withdrawing group. Thus p-nitro aniline will have largest value of pK<sub>b</sub>.</p>
<p>Question 5.<br />
State two important uses of aniline. (DSB 2000)<br />
Answer:</p>
<ol>
<li>In the manufacture of dyes and drugs.</li>
<li>In the preparation of phenyl isocyanide required for the manufacture of polyurethane plastic.</li>
</ol>
<p>Question 6.<br />
Why do amines behave as nucleophiles ?<br />
Answer:<br />
Amines behave as nucleophiles. For eg: amines react with alkyl halides, acid chlorides etc.</p>
<p>Question 7.<br />
Why are aqueous solution of amines basic in nature ? (DSB 2006)<br />
Answer:<br />
Aqueous solution of amines which are freely soluble in water (like CH<sub>3</sub>NH<sub>2</sub>, C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> etc) are basic in nature. It can be explained as follows,<br />
For eg:-<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73037" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-74.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 74" width="270" height="61" /><br />
The aqueous solution of methyl amine will be basic in nature, due to the presence of <img loading="lazy" decoding="async" class="alignnone size-full wp-image-73043" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-75.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 75" width="34" height="29" /> ions.</p>
<p>Question 8.<br />
Explain why silver chloride is soluble in aqueous solution of methyl amine. (CBSE 1997, 1998,2002,2004)<br />
Answer:<br />
Due to the formation of water soluble complex<br />
AgCl + 2CH<sub>3</sub>NH<sub>2 </sub> → [Ag(CH<sub>3</sub>NH<sub>2</sub>)<sub>2</sub>]+Cl</p>
<p>Question 9.<br />
Write IUPAC name of. (Delhi CBSE 1999)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73046" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-76.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 76" width="226" height="61" /><br />
Answer:<br />
p-nitro-N, N dimethyl aniline.</p>
<p>Question 10.<br />
For an amine RNH<sub>2</sub>, write the expression for K<sub>b</sub> to indicate its base strength. (DBS 2000)<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73049" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-77.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 77" width="287" height="104" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 11.<br />
What does K<sub>b</sub> value for an amine stand for? (AISB 2000)<br />
Answer:<br />
K<sub>b</sub> value for an amine stands for its basic strength. More the K<sub>b</sub> value of an amines more is its basic strength.</p>
<p>Question 12.<br />
Give one example of anbident nucleophile. (CBSE 2001)<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73051" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-78.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 78" width="174" height="36" /><br />
acts as ambident nucleophiles.</p>
<p>Question 13.<br />
Why do amines acts as nucleophiles ? (AISB 2007)<br />
Answer:<br />
Aliphatic amines act as nucleophiles. This is due to the availability of lone pair of electrons on nitrogen<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73053" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-79.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 79" width="275" height="88" /><br />
Aromatic amines do not behave as nucleophiles. This is because the lone pair of electrons on nitrogen in aromatic amines is involved in resonance with benzene ring, and as such not available for nucleophije attack.</p>
<p>Question 14.<br />
Write IUPAC name of. (AISB 2004)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73057" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-80.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 80" width="179" height="55" /><br />
Answer:<br />
4 &#8211; Methoxy benzene amine.</p>
<p>Question 15.<br />
How is phenyl aminomethane obtained from phenyl nitrile. (AISB 2004)<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73060" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-81.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 81" width="383" height="95" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-81.png 383w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-81-300x74.png 300w" sizes="auto, (max-width: 383px) 100vw, 383px" /></p>
<p>Question 16.<br />
Why is an alkyl amine more basic than ammonia ? (CBSE Delhi 2009)<br />
Answer:<br />
This is because of the presence of electron releasing alkyl group (positive I effect) which increases the electron density on nitrogen.</p>
<p>Question 17.<br />
Give the IUPAC name of. H<sub>2</sub>N — CH<sub>3</sub>— CH<sub>2</sub> — CH = CH<sub>2</sub> (CBSE Delhi 2010)<br />
Answer:<br />
But-3-en-l-amine.</p>
<h3>2nd PUC Amines Short Answers Questions</h3>
<p>Question 1.<br />
How are the following conversions accomplished<br />
(1) Aniline to chlorobenzene<br />
(2) Nitrobenzene to phenol<br />
(3) Aniline to benzoic acid<br />
Answer:<br />
(1)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73065" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-82.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 82" width="378" height="758" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-82.png 378w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-82-150x300.png 150w" sizes="auto, (max-width: 378px) 100vw, 378px" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 2.<br />
Account for the following observation:<br />
1. Tertiary amine does not undergo acylation reaction<br />
2. Aniline readily reacts with bromine to give 2,4,6- tribromo aniline (CBSE 2002, 2004)<br />
Answer:<br />
1. Tertiary amine do not undergo acylation reaction because they do not contain a H-atom on the N-atom.<br />
2. This is due to the strong activating effect of the amino group, Halogenation of amines occur very fast and halogens enter at all the three (one P-and two o-positions) positions even in the absence of the catalyst.</p>
<p>Question 3.<br />
Give a chemical test to distinguish between aniline and N-methylaniline. (CBSE 2001, 2006)<br />
Answer:<br />
Aniline being a 1° amine gives carbylamine test i.e. on heating with CHCl<sub>3</sub>, in presence of alc. KOH, it gives offensive smell of phenyl isocyanide while N-methyl aniline being a 2° amine does not give this test.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73070" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-83.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 83" width="424" height="150" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-83.png 424w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-83-300x106.png 300w" sizes="auto, (max-width: 424px) 100vw, 424px" /></p>
<p>Question 4.<br />
Write one chemical reaction each to illustrate the following<br />
1. Hoffmann’s bromamide reaction<br />
2. Gabriel phthalimide synthesis (CBSE 2008)<br />
Answer:</p>
<p>1. Carbylamine reaction<br />
1° amines (aromatic/aliphatic) On heating with chloroform and alcoholic solution of KOH gives isocyanides/carbylamines producing unpleasant smell.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73076" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 24(i)" width="548" height="80" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24i.png 548w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24i-300x44.png 300w" sizes="auto, (max-width: 548px) 100vw, 548px" /><br />
2° and 3° (aromatic/aliphatic) do not give this reaction.</p>
<p>2. Diazotisation .<br />
Aromatic 1° amines into diazonium salts by action of HNO<sub>2</sub> and dil HCl at ice cold temperature as HNO<sub>2</sub> and product are unstable at higher temperature.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73080" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 25(i)" width="457" height="107" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25i.png 457w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-25i-300x70.png 300w" sizes="auto, (max-width: 457px) 100vw, 457px" /><br />
3. Hofmann’s bromamide reaction<br />
Involves heating of an amide with bromine and caustic alkali to yield an amine with one carbon less than original amide.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73085" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 26(i)" width="496" height="56" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26i.png 496w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26i-300x34.png 300w" sizes="auto, (max-width: 496px) 100vw, 496px" /><br />
4. Coupling reaction<br />
Diazonium salt acts as electrophile and brings about substitution in electron rich aromatic ring such as phenol and amines. The result is formation of dye.<br />
(i) with phenol &#8211; In basic medium (9 &#8211; 10 pH) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73090" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 27(i)" width="649" height="119" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27i.png 649w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27i-300x55.png 300w" sizes="auto, (max-width: 649px) 100vw, 649px" /></p>
<p>(ii) with amines &#8211; In acidic medium (ph = 4 &#8211; 5) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73091" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 28(i)" width="630" height="81" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28i.png 630w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28i-300x39.png 300w" sizes="auto, (max-width: 630px) 100vw, 630px" /></p>
<p>5. Ammonolysis &#8211; Alkyl halide (1°) react with alcoholic ammonia to form 1°, 2°, 3° amines along with 4°ammonium salts. It is carried out by heating alkyl halide with ale solution of NH3 in sealed tube at 370 K.<br />
If ammonia is used in excess, 1° amine is major product<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73096" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-29i-1.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 29(i)" width="279" height="53" /><br />
If alkyl halide is excess, it forms all 1°, 2°, 3°, 4° ammonium salts<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73100" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 30(i)" width="322" height="96" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30i.png 322w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30i-300x89.png 300w" sizes="auto, (max-width: 322px) 100vw, 322px" /></p>
<p>6. Acetylation<br />
Aliphatic amines:<br />
Introduction of acetyl group (CH<sub>3</sub>CO-) into any molecule.<br />
1° and 2° amines react with acetyl chloride to form amides<br />
But 3° amines has NO H on N, so do not react.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73104" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31i.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 31(i)" width="676" height="350" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31i.png 676w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31i-300x155.png 300w" sizes="auto, (max-width: 676px) 100vw, 676px" /><br />
7. Gabriel phthalimide synthesis<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73108" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 11(ii)" width="647" height="285" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11ii.png 647w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11ii-300x132.png 300w" sizes="auto, (max-width: 647px) 100vw, 647px" /><br />
Reaction between alkyl halide (R &#8211; X) and ammonia gives mixture, of 1°, 2° and 3° amines with tetraalkyl ammonium halide. Mixture is not separable.<br />
To get pure 1° amine, Gabriel phthalimide synthesis is preferred.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 5.<br />
(a) Arrange the following in an increasing order of basic strength in water:<br />
C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH, (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N and NH<sub>3</sub><br />
(b) Arrange the following in increasing order of basic strength in the gas phase<br />
C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>, (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH, (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N and CH<sub>3</sub>NH<sub>2</sub>. (CBSE Delhi 2008)<br />
Answer:<br />
(a) In aqueous solution, basic strength decreases in the order. .<br />
(C<sub>2</sub>H<sub>5</sub>)NH &gt; (C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N &gt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &gt; NH<sub>3</sub><br />
(b) In gaseous phase,(basic strength decreases in the order.<br />
(C<sub>2</sub>H<sub>5</sub>)<sub>3</sub>N &gt; (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub>NH &gt; C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub> &gt; NH<sub>3</sub>.</p>
<p>Question 6.<br />
Give an example for each describe the following reactions.<br />
1. Hoffmann’s bromamide reaction<br />
2. Coupling reaction<br />
3. Gattermann reaction (CBSE 2009)<br />
Answer:<br />
1.</p>
<p>1. Carbylamine reaction<br />
1° amines (aromatic/aliphatic) On heating with chloroform and alcoholic solution of KOH gives isocyanides/carbylamines producing unpleasant smell.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73110" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 24(ii)" width="548" height="80" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24ii.png 548w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-24ii-300x44.png 300w" sizes="auto, (max-width: 548px) 100vw, 548px" /><br />
2° and 3° (aromatic/aliphatic) do not give this reaction.</p>
<p>2. Diazotisation .<br />
Aromatic 1° amines into diazonium salts by action of HNO<sub>2</sub> and dil HCl at ice cold temperature as HNO<sub>2</sub> and product are unstable at higher temperature.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73113" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-259ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 259(ii)" width="457" height="107" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-259ii.png 457w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-259ii-300x70.png 300w" sizes="auto, (max-width: 457px) 100vw, 457px" /><br />
3. Hofmann’s bromamide reaction<br />
Involves heating of an amide with bromine and caustic alkali to yield an amine with one carbon less than original amide.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73115" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 26(ii)" width="496" height="56" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26ii.png 496w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-26ii-300x34.png 300w" sizes="auto, (max-width: 496px) 100vw, 496px" /><br />
4. Coupling reaction<br />
Diazonium salt acts as electrophile and brings about substitution in electron rich aromatic ring such as phenol and amines. The result is formation of dye.<br />
(i) with phenol &#8211; In basic medium (9 &#8211; 10 pH) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73117" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 27(ii)" width="649" height="119" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27ii.png 649w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-27ii-300x55.png 300w" sizes="auto, (max-width: 649px) 100vw, 649px" /></p>
<p>(ii) with amines &#8211; In acidic medium (ph = 4 &#8211; 5) at low temperature (273 &#8211; 278 K)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73119" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 28(ii)" width="630" height="81" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28ii.png 630w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-28ii-300x39.png 300w" sizes="auto, (max-width: 630px) 100vw, 630px" /></p>
<p>5. Ammonolysis &#8211; Alkyl halide (1°) react with alcoholic ammonia to form 1°, 2°, 3° amines along with 4°ammonium salts. It is carried out by heating alkyl halide with ale solution of NH3 in sealed tube at 370 K.<br />
If ammonia is used in excess, 1° amine is major product<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73121" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-29ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 29(ii)" width="279" height="53" /><br />
If alkyl halide is excess, it forms all 1°, 2°, 3°, 4° ammonium salts<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73122" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 30(ii)" width="322" height="96" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30ii.png 322w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-30ii-300x89.png 300w" sizes="auto, (max-width: 322px) 100vw, 322px" /></p>
<p>6. Acetylation<br />
Aliphatic amines:<br />
Introduction of acetyl group (CH<sub>3</sub>CO-) into any molecule.<br />
1° and 2° amines react with acetyl chloride to form amides<br />
But 3° amines has NO H on N, so do not react.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73123" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31ii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 31(ii)" width="676" height="350" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31ii.png 676w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-31ii-300x155.png 300w" sizes="auto, (max-width: 676px) 100vw, 676px" /><br />
7. Gabriel phthalimide synthesis<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73124" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11iii.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 11(iii)" width="647" height="285" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11iii.png 647w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-11iii-300x132.png 300w" sizes="auto, (max-width: 647px) 100vw, 647px" /><br />
Reaction between alkyl halide (R &#8211; X) and ammonia gives mixture, of 1°, 2° and 3° amines with tetraalkyl ammonium halide. Mixture is not separable.<br />
To get pure 1° amine, Gabriel phthalimide synthesis is preferred.</p>
<p>2. The reaction of diazonium salt with phenols and aromatic amines to form azo compounds of the general formula Ar &#8211; N = N &#8211; Ar is called coupling reaction. The coupling with phenol takes place in mildly alkaline medium while with amines it occurs under faintly acidic condition.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73126" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-84.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 84" width="499" height="122" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-84.png 499w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-84-300x73.png 300w" sizes="auto, (max-width: 499px) 100vw, 499px" /><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73127" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-85.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 85" width="466" height="372" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-85.png 466w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-85-300x239.png 300w" sizes="auto, (max-width: 466px) 100vw, 466px" /></p>
<p>3. Gattermann reaction<br />
When benzene diazonium chloride reacts with Halogen acids in presence of Cu powder, aryl halide is formed as.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73130" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-86.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 86" width="371" height="327" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-86.png 371w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-86-300x264.png 300w" sizes="auto, (max-width: 371px) 100vw, 371px" /></p>
<p>Question 7.<br />
Complete the following reaction equation ?<br />
(1)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73132" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-87.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 87" width="217" height="66" /><br />
(2) C6HSN2CI + H3PO2 + H2O →<br />
(3) C6H5NH2 + Br2 (aq) 4<br />
Answer:<br />
(1)<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-73133" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-13-Amines-88.png" alt="2nd PUC Chemistry Question Bank Chapter 13 Amines - 88" width="291" height="64" /><br />
(2) and (3) Same as NCRT text book Q.No. 11.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10253</post-id>	</item>
		<item>
		<title>2nd PUC Economics Question Bank Chapter 3 Demand Analysis</title>
		<link>https://ktbssolutions.com/2nd-puc-economics-question-bank-chapter-3/</link>
		
		<dc:creator><![CDATA[Prasanna]]></dc:creator>
		<pubDate>Tue, 14 Jul 2026 07:21:44 +0000</pubDate>
				<category><![CDATA[2nd PUC]]></category>
		<guid isPermaLink="false">https://ktbssolutions.com/?p=10133</guid>

					<description><![CDATA[You can Download Chapter 3 Demand Analysis Questions and Answers, Notes, 2nd PUC Economics Question Bank with Answers Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations. Karnataka 2nd PUC Economics Question Bank Chapter 3 Demand Analysis 2nd PUC Economics Demand Analysis One Mark Questions and Answers [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>You can Download Chapter 3 Demand Analysis Questions and Answers, Notes, <a href="https://ktbssolutions.com/2nd-puc-economics-question-bank/">2nd PUC Economics Question Bank with Answers</a> Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations.</p>
<h2>Karnataka 2nd PUC Economics Question Bank Chapter 3 Demand Analysis</h2>
<h3>2nd PUC Economics Demand Analysis One Mark Questions and Answers</h3>
<p>Question 1.<br />
What is Demand?<br />
Answer:<br />
The concept ‘demand’ refers to the quantity of a good or service that a consumer is willing and able to purchase at various prices, during a period of time. It includes desire for a commodity, ability to pay and willingness to pay.</p>
<p>Question 2.<br />
Qd = f(p) is the demand function. Identify the independent variable in it.<br />
Answer:<br />
In Qd = f(p), the independent variable is ‘p’ (price).</p>
<p>Question 3.<br />
State the Law of Demand.<br />
Answer:<br />
The law can be explained in the following manner: “Other things being equal, a fall in price leads to expansion in demand and a rise in price leads to contraction in demand”.</p>
<p>Question 4.<br />
What is the relationship between price and demand for complementary goods?<br />
Answer:<br />
There is an inverse relationship between price and demand for complementary goods. (When the price of a product becomes more, the demand for its complementary good falls).</p>
<p>Question 5.<br />
What are normal goods?<br />
Answer:<br />
Normal goods are those goods for which the demand increases with rise in income of consumers , and decreases with fall in their income.</p>
<p>Question 6.<br />
Why does the demand curve shift?<br />
Answer:<br />
The shift in demand curve occurs because of changes in all the determinants of demand except price.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 7.<br />
Name the method of adding two individual demand curves horizontally.<br />
Answer:<br />
The method of adding two individual demand curves is ‘Horizontal summation’.</p>
<p>Question 8.<br />
Give the meaning of elasticity of demand.<br />
Answer:<br />
Elasticity of demand is generally defined as the responsiveness or sensitiveness of demand to a given change in the price of commodity.</p>
<p>Question 9.<br />
Write the simplified formula of income elasticity of demand.<br />
<img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176661456_1c16da835a_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 1" width="101" height="44" /></p>
<p>Question 10.<br />
If change in price and change in expenditure are in the same direction, then what will be the price elasticity of demand?<br />
Answer:<br />
If change in price and change in expenditure are in the same direction, the price elasticity of demand is less than one, i.e., less elastic demand. (P<sub>ed</sub> &lt;1).</p>
<p>Question 11.<br />
What is Cross Elasticity of Demand?<br />
Answer:<br />
It may be defined as the proportionate change in the quantity demanded of a particular commodity in response to a change in the price of another related commodity.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 12.<br />
What is demand function?<br />
Answer;<br />
The Demand Function refers to a functional relationship between quantities demanded and its determinants. It can be expressed as follows:<br />
Qd = f(P, Pr ,Y, T,&#8230;&#8230;&#8230;&#8230;.. ).<br />
Where Qd stands for Quantity demanded, f is function, P is Price of commodity, Pr &#8211; price of related/substitutes, Y is income of consumers, T is tastes and preferences of consumers.</p>
<h3>2nd PUC Economics Demand Analysis Two Marks Questions and Answers</h3>
<p>Question 1.<br />
Mention any four determinants of demand.<br />
Answer:</p>
<ol>
<li>Price of the product</li>
<li>Price of related goods</li>
<li>Income of consumers and</li>
<li>Tastes and preferences of consumers.</li>
</ol>
<p>Question 2.<br />
In Qd = 20 &#8211; 2p, identify independent variable, dependent variable, constant and co-efficient in it.<br />
Answer:<br />
Qd is dependent variable, P is independent variable, 20 is constant, -2 is coefficient of ‘p&#8217;</p>
<p>Question 3.<br />
If Qd = 30 &#8211; 2p is the demand function. Suppose the price of onion in the market is Rs.10 per kg. Calculate the quantity demanded.<br />
Answer:<br />
Qd = 30 &#8211; 2p; If price is Rs. 10,<br />
Qd = 30 &#8211; 2(10)<br />
= 30 &#8211; 20<br />
= 10.<br />
The quantity demanded of onion is 10 kgs.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 4.<br />
Why does the demand curve slope downwards?<br />
Answer:<br />
The demand curve slopes downwards because of price effect, substitution effect, income effect and operation of law of diminishing marginal utility.</p>
<p>Question 5.<br />
Write the meaning of cross elasticity of demand and its formula.<br />
Answer:<br />
It may be defined as the proportionate change in the quantity demanded of a particular commodity in response to a change in the price of another related commodity</p>
<p><img loading="lazy" decoding="async" src="https://live.staticflickr.com/65535/49201881103_e03fba0bdd_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 2" width="497" height="129" /></p>
<p>Question 6.<br />
What are complementary goods? Give examples.<br />
Answer:<br />
Complementary goods are those goods which are consumed together or jointly to satisfy human wants. Example, Shoes and socks, vehicles and petrol, bat and ball etc.</p>
<p>Question 7.<br />
Consider the demand for onion. At Rs.10 per kg, demand for onion is 15 kgs. Suppose the price increases to Rs.20 per kg, the demand decreases to 10 kgs. Calculate the price elasticity of demand.<br />
Answer:<br />
Solution:<br />
∆q = 10 &#8211; 15 = -5; ∆p = 20 &#8211; 10 = 10; then PED is<br />
<img loading="lazy" decoding="async" src="https://live.staticflickr.com/65535/49176172548_ecc3a54f2c_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 3" width="111" height="101" /><br />
= -0.33 (the Price Elasticity is 0.33)</p>
<p>Question 8.<br />
There are only two consumers in a market X and Y. Their demand for a good is given below. Calculate the market demand for the goods and draw the market demand curve.</p>
<table border="2" width="631">
<tbody>
<tr>
<td width="158">
<p style="text-align: center;"><strong>Price</strong></p>
</td>
<td style="text-align: center;" width="158"><strong>Demand- X</strong></td>
<td style="text-align: center;" width="158"><strong>Demand-Y</strong></td>
<td width="158">
<p style="text-align: center;"><strong>Market Demand (x + y)</strong></p>
</td>
</tr>
<tr>
<td width="158">
<p style="text-align: center;">2</p>
</td>
<td style="text-align: center;" width="158">16</td>
<td style="text-align: center;" width="158">20</td>
<td style="text-align: center;" width="158">36</td>
</tr>
<tr>
<td width="158">
<p style="text-align: center;">4</p>
</td>
<td style="text-align: center;" width="158">14</td>
<td style="text-align: center;" width="158">18</td>
<td style="text-align: center;" width="158">32</td>
</tr>
<tr>
<td width="158">
<p style="text-align: center;">6</p>
</td>
<td style="text-align: center;" width="158">12</td>
<td style="text-align: center;" width="158">15</td>
<td width="158">
<p style="text-align: center;">27</p>
</td>
</tr>
<tr>
<td style="text-align: center;" width="158">8</td>
<td style="text-align: center;" width="158">10</td>
<td style="text-align: center;" width="158">12</td>
<td width="158">
<p style="text-align: center;">22</p>
</td>
</tr>
<tr>
<td style="text-align: center;" width="158">10</td>
<td style="text-align: center;" width="158">8</td>
<td style="text-align: center;" width="158">10</td>
<td width="158">
<p style="text-align: center;"><sup>18</sup></p>
</td>
</tr>
<tr>
<td width="158">
<p style="text-align: center;">12</p>
</td>
<td style="text-align: center;" width="158">6</td>
<td style="text-align: center;" width="158">8</td>
<td width="158">
<p style="text-align: center;">14</p>
</td>
</tr>
</tbody>
</table>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176661381_2ec5c063bb_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 4" width="394" height="299" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 9.<br />
If there are two consumers in a market and their individual demand functions are Qd<sub>1</sub> = 15 &#8211; 2p and Qd<sub>2</sub> = 25 &#8211; 3p. Find the Market demand function.<br />
Answer:<br />
The market demand function Qd = Qd<sub>1</sub>+ Qd<sub>2</sub><br />
Therefore,<br />
Qd = 15 &#8211; 2p + 25 &#8211; 3p<br />
Qd = 40 &#8211; 5p</p>
<p>When the price is ‘0’, quantity demanded will be<br />
Qd = 40 &#8211; 5p<br />
= 40 &#8211; 5(0)<br />
=40</p>
<p>When the quantity demanded is ‘0’, the price will be<br />
0 = 40 &#8211; 5p<br />
40 &#8211; 5p = 0<br />
40 = 5p<br />
P = 40/5<br />
P = 8<br />
So the Market demand is ‘40’ and Market price is Rs.8.</p>
<p>Question 10.<br />
How do the movements along the demand curve occur?<br />
Answer:<br />
The movements along the demand curve occur on the basis of the inverse relationship between price and quantities demanded. When the price is less, demand will be more and when the price is more, demand will be less. So, any changes in price lead to movement on the demand line.</p>
<h3>2nd PUC Economics Demand Analysis Five Marks Questions and Answers</h3>
<p>Question 1.<br />
Why does the demand curve slope downwards? Explain.<br />
Answer:<br />
In order to represent the inverse relationship between price and demand, the demand curve must slope downwards. Apart from this basic reason, there are many other factors which make the demand curve to slope downwards. They are as follows:</p>
<p>(a) Operation of the law of Diminishing Marginal Utility:<br />
The law of DMU states that as the consumer acquires larger quantities of any commodity, the additional units of        the same product will give him lower utility, and as such he gets a less value for the additional under The law of        demand states that in order to induce the consumer to buy more less price must be offered.</p>
<p>(b) Operation of the law of Equi &#8211; Marginal Utility:<br />
This law states that utility of the product must be equal to its price in general. As price falls, the equality between the two will be disturbed and in order to re-establish this equality the consumer buys more. Now utility comes to the level of reduced price. Hence, as price falls, a consumer buys more.</p>
<p>(c) Income effect:<br />
A change in demand as a result of change in income is called as Income effect. As price falls, the real income of the consumer increases. With this increased real income (gets more purchasing power with more money in his hands), he buys more.</p>
<p>(d) Substitution effect:<br />
When the price of one product falls, it becomes cheaper when compared to other products ’ for which price remains constant. Hence, a consumer will substitute low priced product to high priced product. The result is that demand for a product rises as price falls.</p>
<p>(e) Price Effect:<br />
When the change in quantities demanded is caused by the change in price, it is called as Price effect. When the price of a product falls, it becomes cheaper and consumer buys more of that and vice versa.<br />
Hence, the demand curve always slopes downwards from left to right.</p>
<p>Question 2.<br />
How does the demand curve shift? Explain with a diagram.<br />
Answer:<br />
(a) Shift in demand curve &#8211; Increase and Decrease in Demand:<br />
The increase and decrease in demand are caused by all the determinants of demand except price. When there is change in consumer’s income, tastes and preferences, price of related goods, there may be increase or decrease in demand.</p>
<p>(b) Increase in Demand:<br />
When the income of consumer increases, the demand for the product increases and there will be shift in demand line towards right. For normal goods, the demand, curve shifts to the right. In the diagram given below, D:                  represents shift in demand line towards right indicating increase in demand.</p>
<p>(c) Decrease in Demand:<br />
When the price of related goods rise, the demand for the product falls and the demand curve shifts towards left.      For example, if there is rise in price of petrol, the demand for vehicle decreases, representing backward shift of demand line. In the diagram below, D<sub>2</sub> represents shift in demand towards left indicating decrease in demand.</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176661341_5701286e22_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 5" width="258" height="228" /></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 3.<br />
What is income elasticity of demand? Calculate the income elasticity of demand when income of consumer increases from Rs.10,000 to Rs.12,000 and demand for rice increases from 30 to 40 kgs.<br />
Answer:<br />
Income elasticity of demand may be defined as the ratio or proportionate change in the quantity demanded of a commodity to a given proportionate change in the income. In short, it indicates the extent to which demand changes with a variation in consumers income.</p>
<p>The following formula helps to measure Y<sub>ed</sub></p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176661326_b6638c136e_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 6" width="269" height="122" /></p>
<p>Here, ∆q stands for change in quantity, ∆y is change in Income of consumer, ‘y’ is initial income and ‘q’ is initial quantity.</p>
<p>Solution:<br />
∆q = 40 -30 = 10;       ∆y = 12,000 &#8211; 10,000 = 2000; then Y<sub>ed</sub> is ;<br />
<img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176877057_33bfb54ede_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 7" width="220" height="112" /></p>
<p>= 1.66 Therefore the Income Elasticity of Demand is greater than one.</p>
<p>Question 4.<br />
What are the factors determining price elasticity of demand?<br />
Answer:<br />
(i) Nature of the Commodity:<br />
In case of comforts and luxuries, demand tends to be elastic because people buy those more only when their prices are low. e.g. TV sets.</p>
<p>In case of necessaries, demand is inelastic because whatever may be the price, people have to buy and use them.      e.g. Rice.</p>
<p>(ii) Existence of Substitutes:<br />
If a product has substitutes, demand tends to become elastic because people compare tho prices of substitute goods and cheaper products are purchased, eg. Blades, Soaps.</p>
<p>If a product has no substitutes, demand becomes inelastic because in that case whatever may be the price,                people have to buy them. e.g. Onion.</p>
<p>(iii) Durability of the commodity:<br />
If a product is perishable or non durable, demand tends to be inelastic, because people buy them again and again.<br />
If a product is durable, demand tends to be elastic because people buy them occasionally.</p>
<p>(iv) Number of uses of a commodity:<br />
If a product has multiple uses, demand tends to become elastic because, with a fall in price, the same product can be used for many purposes, e.g. Electricity, coal etc.</p>
<p>If a product has only one use, in that case demand becomes inelastic because people have to buy them for a            specific single purpose whatever may be the price, e.g. All eatables, seeds, fertilizers, pesticides etc.</p>
<p>(v) Possibility of postponing the use of product:<br />
If there is a possibility to postpone the use of particular product, demand tends to become elastic, e.g. Buying a          scooter, motorcycle, TV sets etc. people generally buy these articles when they are cheaper. .</p>
<p>If it is not possible to postpone, demand tends to become inelastic. In this case, whatever may be the price,                people have to buy them. e.g. Medicine.</p>
<p>(vi) Level of income of the people:<br />
Generally speaking, demand will be elastic in case of the poor people because even a small change in price will affect the demand for various products.</p>
<p>On the other hand demand will be inelastic in case of rich people because they are ready to spend any amount on buying a product.</p>
<p>(vii) Habits:<br />
If people are not habituated for the use of certain products, then demand tends to be elastic. If products are cheaper, they buy more and if they become costly, they may buy less or may not buy them at all.</p>
<p>When people are habituated for the use of a particular commodity, they do not care for price changes over a              certain range, e.g. Cigarettes,, liquor etc. In that case, demand tends to become inelastic.</p>
<p>(viii) Complementary goods:<br />
Goods which are jointly demanded are inelastic in nature, e.g., ink and pens, vehicles and petrol etc. This is because, if people buy one product, they have to buy the supplementary products also without which they cannot make use of the first item.</p>
<p>Demand tends to be elastic in case of independent products, e.g., biscuits, chocolates, ice-creams etc. In this case, consumption or use of a product is not linked to any other products. Hence, they may or may not buy a              product.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<h3>2nd PUC Economics Demand Analysis Ten Marks Questions and Answers</h3>
<p>Question 1.<br />
Explain the law of demand with the help of demand schedule and demand curve.<br />
Answer:<br />
The law can be explained in the following manner: “Other things being equal, a fall in price leads to expansion in demand and a rise in price leads to contraction in demand&#8221;.</p>
<p>According to Prof.Samuelson, the law of demand states that ‘People buy more at lower prices and buy less at higher prices, other things remaining the same’.</p>
<p>Demand schedule:<br />
Demand schedule represents the quantities demanded by an individual consumer at different levels of price.</p>
<p style="text-align: center;"><strong>        Individual Demand Schedule</strong></p>
<table border="2">
<tbody>
<tr>
<td width="138">
<p style="text-align: center;"><strong>Price P (in Rs.)</strong></p>
</td>
<td width="144">
<p style="text-align: center;"><strong>Demand (Qd) (in Kg)</strong></p>
</td>
</tr>
<tr>
<td width="138">
<p style="text-align: center;">3</p>
</td>
<td style="text-align: center;" width="144">30</td>
</tr>
<tr>
<td width="138">
<p style="text-align: center;">4</p>
</td>
<td style="text-align: center;" width="144">25</td>
</tr>
<tr>
<td width="138">
<p style="text-align: center;">5</p>
</td>
<td width="144">
<p style="text-align: center;">20</p>
</td>
</tr>
<tr>
<td style="text-align: center;" width="138"><sup>6</sup></td>
<td width="144">
<p style="text-align: center;">15</p>
</td>
</tr>
<tr>
<td style="text-align: center;" width="138">7</td>
<td width="144">
<p style="text-align: center;">10</p>
</td>
</tr>
</tbody>
</table>
<p>In the above individual demand schedule, the consumer is purchasing different quantities at different price levels. At Rs.3 he buys 30 kgs, and at Rs. 4, 25 kgs are bought and so on. As the price increases, the quantities demanded falls.</p>
<p>Demand Curve: The graphical presentation of the demand schedule is called demand curved</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176172373_c5f35b2fc4_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 8" width="268" height="235" /><br />
<img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>In the above diagram, price is measured along y axis and quantities demanded are measured along x axis. The various points on Demand line represent the respective quantities demanded. For example, point ‘c’, quantities demanded is 20 at price Rs.5.</p>
<p>The demand curve slopes downwards from left to right. It shows the rate at which demand changes with respect to change in price. As there is an inverse relationship between price and quantities demanded, the curve is negatively sloped.</p>
<p>Question 2.<br />
Classify the price elasticity of demand and explain them with diagrams.<br />
Answer:<br />
In the words of Prof. Stonier and Hague, “Price elasticity of demand is a technical term used by economists to describe the degree of responsiveness of the demand for a good to a change in its price.”<br />
It is measured by using the following formula.</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176172353_d975dcec05_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 9" width="309" height="50" /></p>
<p>The rate of change in demand may not always be proportionate to the change in price. A small change in price may lead to very great change in demand. It is called as Elastic Demand. Sometimes even a big change in price may not cause any change in demand. Such a demand is known as Inelastic Demand.</p>
<p>The following formula is used to calculate Price Elasticity of Demand (P<sub>ed</sub>):<br />
<img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176876972_32e220a4c9_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 10" width="104" height="52" /><br />
Here, ∆q stands for change in quantity, ∆p is change in price, ‘p’ is the initial price and &#8216;q&#8217; is the initial quantity.</p>
<p>Classification of Price Elasticity of Demand:<br />
On the basis of the degree of price elasticity for different goods, we classify P<sub>ed</sub> as follows:</p>
<p>1. Perfectly Elastic Demand:<br />
In this case, a very small change in price leads to an infinite change in demand. The demand curve is a horizontal curve and parallel to x axis. The numerical co-efficient of perfectly elastic demanded is infinity (ED = ∞).</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176172298_225ccf8ffb_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 11" width="189" height="156" /></p>
<p>2. Perfectly Inelastic Demand:<br />
In this case, whatever may be the change in price, quantity demanded will remain perfectly constant. The demand curve is a vertical straight line and parallel to Y axis. Quantity demanded would be 10 units, irrespective of price change from Rs. 10.00 to Rs.2.00. Hence, the numerical co-efficient of perfectly inelastic demand is zero. ED = 0.</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176661151_c69ce901d9_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 12" width="270" height="192" /></p>
<p>3.Relatively Elastic Demand: More elastic demand.<br />
In this case, a slight change in price leads to more than proportionate change in demand. One can notice here that a change in demand is more than that of change in price. Hence, the elasticity is greater than one. For e.g., price falls by 3% and demand rises by 9%. Hence, the numerical co-efficient of demand is greater than one.</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176876897_44598ca409_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 13" width="291" height="196" /></p>
<p>Here, the percentage change in quantities demanded will be more than percentage change in price,                        i.e., ∆q &gt; ∆p. M M<sub>1</sub> &gt; P P<sub>1</sub>.</p>
<p>4. Relatively Inelastic Demand: Less elastic demand. In this case, a large change in price, say 8% price fall, leads to less than proportionate change in demand: say 4% rise in demand. One can notice here that change in demand is less than that of change in price. This can be represented by a steeper demand curve. Here, elasticity is less than one. (P<sub>ed</sub> &lt;1)</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176172173_76cea2bcfd_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 14" width="273" height="206" /></p>
<p>Here, the percentage change in quantities demanded will be less than percentage change in price, i.e., ∆q &gt; ∆p, M M<sub>1 </sub>&gt; P P<sub>1</sub></p>
<p>5. Unitary Elastic Demand:<br />
In this case, proportionate change in price leads to Equal proportionate change in demand. For e.g., 5% fall in price leads to exactly 5% increase in demand. Hence, elasticity is equal to unity. It is possible to come across unitary elastic demand, but it is a rare phenomenon.</p>
<p><img loading="lazy" decoding="async" class="alignnone" src="https://live.staticflickr.com/65535/49176876812_28c447b5a4_o.png" alt="2nd PUC Economics Question Bank Chapter 3 Demand Analysis 15" width="276" height="190" /></p>
<p>Here, the percentage change in quantities demanded will be equal to percentage change in price.                            i.e., ∆q &gt; ∆p, M M <sub>1</sub> &gt; P P<sub>1.</sub></p>
<p>Out of the five different degrees, the first two are theoretical and the last one is a rare possibility. Hence, in all our general discussions, we make reference only to two terms- relatively classic demand and relatively inelastic demand.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10133</post-id>	</item>
		<item>
		<title>2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry</title>
		<link>https://ktbssolutions.com/2nd-puc-chemistry-question-bank-chapter-3/</link>
		
		<dc:creator><![CDATA[Prasanna]]></dc:creator>
		<pubDate>Tue, 14 Jul 2026 06:24:41 +0000</pubDate>
				<category><![CDATA[2nd PUC]]></category>
		<guid isPermaLink="false">https://ktbssolutions.com/?p=10172</guid>

					<description><![CDATA[You can Download Chapter 3 Electrochemistry Questions and Answers, Notes, 2nd PUC Chemistry Question Bank with Answers Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations. Karnataka 2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry 2nd PUC Chemistry Electrochemistry NCERT Textbook Questions and Answers Question 1. Arrange the [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>You can Download Chapter 3 Electrochemistry Questions and Answers, Notes, <a href="https://ktbssolutions.com/2nd-puc-chemistry-question-bank/">2nd PUC Chemistry Question Bank with Answers</a> Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations.</p>
<h2>Karnataka 2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry</h2>
<div class="OD">
<div class="IL">
<div id=":ks.av" class="Up pC">
<h3 class="n291pb uaxL4e">2nd PUC Chemistry Electrochemistry NCERT Textbook Questions and Answers</h3>
<p>Question 1.<br />
Arrange the following metals in the order in which they displace each other from the solution of their salts.<br />
Al, Cu, Fe, Mg and Zn.<br />
Answer:<br />
Mg, Al, Zn, Fe, Cu.</p>
<p>Question 2.<br />
Given the standard electrode potentials, K<sup>+</sup>/K = -2.93V, Ag<sup>+</sup>/Ag = 0.80V,<br />
Hg<sup>2+</sup>/Hg = 0.79 V<br />
Mg<sup>2+</sup>/Mg = -2,37 V, Cr<sup>3+</sup>/Cr = &#8211; 0.74V<br />
Arrange these metals in their increasing order of reducing power.<br />
Answer:<br />
The lower the reduction potential, the higher is the reducing power. Hence, the reducing power of the given metals increases inthe following order.<br />
Ag &lt; Hg &lt; Cr &lt; Mg &lt; K.</p>
<p>Question 3.<br />
Depict the galvanic cell in which the reaction Zn(s)+2Ag<sup>+</sup>(aq) —&gt; Zn<sup>2+</sup>(aq)+2Ag(s) takes place. Further show:<br />
(i) Which of the electrode is negatively charged?<br />
(ii) The carriers of the current in the cell.<br />
(iii) Individual reaction at each electrode.<br />
Answer:<br />
The galvanic cell in which the given reaction takes place is depicted as:<br />
Zn(s) | Zn<sup>2+</sup> (aq) || Ag<sup>+</sup> (aq) | Ag(s)<br />
(i) Zn electrode (anode) is negatively charged<br />
(ii) Tons are carriers of current in the cell and in the external circuit, current from silver to Zinc.<br />
(iii) The reaction taking place at the anode is given by,<br />
Zn(s) -H → Zn<sup>2+</sup>(aq) + 2e<sup>&#8211;</sup><br />
The reaction taking place at the cathode is given<br />
Ag<sup>+</sup>+ e<sup>&#8211;</sup> → Ag(s)</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 4.<br />
Calculate the standard cell potentials of galvanic cell in which the following reactions take place:<br />
(i) 2Cr(s) + 3Cd<sup>2+</sup>(aq) → 2Cr<sup>3+</sup>(aq) + 3Cd<br />
(ii) Fe<sup>2+</sup>(aq) + Ag<sup>+</sup>(aq) → Fe<sup>3+</sup>(aq) + Ag(s)<br />
Calculate the ArG9and equilibrium constant of the reactions.<br />
Answer:<br />
(i) For the given reaction, the Nemst equation can be given as:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72131" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-1.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 1" width="373" height="327" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-1.png 373w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-1-300x263.png 300w" sizes="auto, (max-width: 373px) 100vw, 373px" /><br />
∴ E<sup>θ</sup> = 1.104V<br />
We know that,<br />
Δ<sub>r</sub>G<sup>θ</sup> = -nFE<sup>θ</sup><br />
= -2 × 96487× 1.04<br />
= &#8211; 213043.296J<br />
= -213.04KJ</p>
<p>Question 5.<br />
Write the Nernst equation and em! of the<br />
following cells at 298 K:<br />
(I) Mg(s)|Mg<sup>+2</sup>(O.OO1M) ||Cu<sup>+2</sup>(0.0001M)|Cu(s) .<br />
(ii) Fe(s)|Fe<sup>+2</sup>(O.OO1 M)||H<sup>+</sup>(1M)H<sub>2</sub>(g) (1bar)|Pt(s)<br />
(iii) Sn(s) |Sn<sup>2+</sup>(O.050 M)||H<sup>+</sup>(0.020M|H2(g) (1 bar)|Pt(s)<br />
(iv) Pt(s)|Br<sub>2</sub>(l)|Br<sup>&#8211;</sup>(O.O1O M)||H<sup>+</sup>(O.030 M)| H<sub>2</sub>(g) (1 bar)|Pt(s).<br />
Answer:<br />
(i) E<sup>θ</sup>Cr<sup>3+</sup> /Cr = 0.74V<br />
E<sup>θ</sup>Cd<sup>2+</sup> / Cd = &#8211; 0.40V<br />
The galvanic cell of the reaction IC depicted as :<br />
Cr(s)|Cr<sup>3+</sup> (aq) || (Cd<sup>2+</sup> (aq) Cd(s)<br />
Now, the standard cell potential is<br />
E<sup>θ</sup><sub>cell</sub> = E<sup>θ</sup><sub>R</sub>&#8211; E<sup>θ</sup>L<br />
= -40 &#8211; (-0.74)<br />
= +0.34V<br />
∆<sub>r</sub>G<sup>θ</sup> = —nFE<sup>θ</sup><sub>cell</sub><br />
In the given equation,<br />
n = 6<br />
F = 96487 C mol<sup>-1</sup><br />
E<sup>θ</sup><sub>cell</sub> = + 0.34V<br />
Then, ∆<sub>r</sub>G<sup>θ</sup> =-6 × 96487 mol<sup>-1</sup> × 0.34V<br />
= -196833.48 CV mol<sup>-1</sup><br />
= -196833.48 J mol<sup>-1</sup><br />
= -196.83 KJ mol<sup>-1</sup><br />
Again<br />
∆<sub>r</sub>G<sup>θ</sup> = -RT In K<br />
=&gt;∆<sub>r</sub>G<sup>θ</sup> =-2.303RT log K<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72132" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-2.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 2" width="292" height="186" /></p>
<p>(ii) E<sub>θ</sub> Fe<sup>3+</sup> /Fe<sup>2+</sup> = 0.77V<br />
E<sub>θ</sub> Ag<sup>&#8211;</sup>/Ag = 0.80V<br />
(ii) For the given reaction, the Nernst equation can be given as:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72135" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-3.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 3" width="295" height="201" /></p>
<p>(iii) Far the givën reaction, the Nernst equation can be given as:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72138" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-4.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 4" width="255" height="53" /><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72140" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-5.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 5" width="286" height="51" /></p>
<p>0.14 &#8211; 0.0295 × log 125<br />
= 0.14-0.062<br />
= 0.078 V<br />
= 0.08 V (approx)</p>
<p>(iv) For the given reaction , the nernst equation can be given as:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72142" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-6.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 6" width="374" height="239" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-6.png 374w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-6-300x192.png 300w" sizes="auto, (max-width: 374px) 100vw, 374px" /><br />
= &#8211; 1.09 &#8211; 0.02955 × log ( 1.11× 10<sup>7</sup>)<br />
= &#8211; 1.09 &#8211; 0.02955(0.0453 + 7)<br />
= -1.09 &#8211; 0.208 =-1.298 V.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 6.<br />
In the button cells widely used in watches and other devices the following reaction takes place:<br />
Zn(s) + Ag<sub>2</sub>O(s) + H<sub>2</sub>O(l) → Zn<sup>2 </sup>+ (aq) + 2Ag(s) + 2OH-(aq)<br />
Determine ∆<sub>r</sub> G<sup>θ</sup> and E<sup>θ</sup> for the reaction.<br />
Answer:<br />
The galvanic cell of the reaction is depicted as:<br />
Fe<sup>2+</sup> (aq) | Fe<sup>3+</sup> (aq) || Ag<sup>+</sup> (aq) | Ag(s)<br />
Now, the standard cell potential is<br />
E<sup>θ</sup><sub>cell</sub> = E<sup>θ</sup><sub>R</sub> &#8211; El<sup>θ</sup><br />
= 0.80 &#8211; 0.77 &#8216;<br />
= 0.03 V<br />
Here, n = 1<br />
Then, ∆<sub>r</sub> G<sup>θ</sup> = &#8211; nFE<sup>θ</sup><sub>cell</sub><br />
= -1 × 96487 C mol<sup>-1</sup> × 0.03V<br />
= &#8211; 2894.61 J mol<sup>-1</sup><br />
= &#8211; 2.89 KJ mol<sup>-1</sup><br />
∆<sub>r</sub> G<sup>θ</sup> = 2.303 RT In K<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72144" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-7.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 7" width="331" height="188" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-7.png 331w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-7-300x170.png 300w" sizes="auto, (max-width: 331px) 100vw, 331px" /></p>
<p>Question 7.<br />
Define conductivity and molar conductivity for the solution of an electrolyte.<br />
Discuss their variation with concentration.<br />
Answer:<br />
Conductivity of a solution is defined as the conductance of a solution 1 cm in length and area of cross section cm2.1 is represented by K.</p>
<p>Conducti vity always decreases with a decrease in concentration both for weak and strong electrolytes. This is because the number of ions per unit volume that carry the current in a solution decreases with a decrease in concentration.</p>
<p>Molar conductivity of a solution at a given concentration is the conductance of volume V of a solution containing 1 mole of the electrolyte kept between two electrodes with the area area of cross-section A and distance of unit length.</p>
<p>Molar conductivity increases with a decrease in concentration. This is because the total volume of the solution containing one mole of the electrolyte increases on dilution.</p>
<p>Question 8.<br />
The conductivity of 0.20 M solution of KCl at 298 K is 0.0248 S cm<sup>-1</sup>. Calculate its molar conductivity.<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72147" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-8.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 8" width="341" height="55" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-8.png 341w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-8-300x48.png 300w" sizes="auto, (max-width: 341px) 100vw, 341px" /></p>
<p>Question 9.<br />
The resistance of a conductivity cell containing 0.001M KCl solution at 298 K is 1500Ω. What is the cell constant if conductivity of 0.001M KCl solution at 298 K is 0.146 × 10<sup>-3</sup> S cm<sup>-1</sup>.<br />
Answer:<br />
Cell constant = conductivity × Resistance<br />
= 0.146 × 10<sup>-3</sup>S C<sup>m-1</sup> × 1500 Ω = 0.219 cm<sup>-1</sup></p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 10.<br />
The conductivity of sodium chloride at 298 K has been determined at different concentrations and thfe results are given below:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72148" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-9.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 9" width="363" height="64" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-9.png 363w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-9-300x53.png 300w" sizes="auto, (max-width: 363px) 100vw, 363px" /></p>
<p>Calculate ∆<sub>m</sub> for all concentrations and draw a plot between ∆<sub>m</sub> and c<sup>1/2</sup>. Find the value of ∆<sup>0</sup><sub>m</sub><br />
Answer:<br />
K = 7.896 × 10<sup>-5</sup> S cm<sup>-1</sup><br />
M = 0.00241<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72149" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-10.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 10" width="355" height="187" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-10.png 355w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-10-300x158.png 300w" sizes="auto, (max-width: 355px) 100vw, 355px" /></p>
<p>Question 11.<br />
How much charge is required for the following reductions?<br />
(i) 1 mol of Al<sup>3+</sup> to Al<br />
(ii) 1 mol of Cu<sup>2+</sup> to Cu<br />
(iii) 1 mol of MnO<sup>4-</sup> to Mn<sup>2+</sup><br />
Answer:<br />
Al<sup>3+</sup> + 3e → A1<br />
charge required = 3F<br />
(ii) Cu<sup>2+</sup> + 2e → Cu<br />
charge required = 2F<br />
(iii) MnO<sup>4-</sup> + 8H<sup>+</sup> + Se<sup>&#8211;</sup> → Mn<sup>2+</sup> + H<sub>2</sub>O<br />
charge required = 5F</p>
<p>Question 12.<br />
How much electricity in terms of Faraday ¡s required to produce<br />
(j) 20.Ogat Ca from molten CaCl<sub>2</sub><br />
(ii) 40.0 g of Al from Almólten Al<sub>2</sub>O<sub>3</sub><br />
Answer:<br />
(i) Ca<sup>2+</sup>2 + 2e → Ca<br />
2F can produce I mole (=40 g) Ca<br />
∴ To produce 20 g Ca requires, \(\frac{2 \mathrm{F} \times 20}{40}\) = 1F</p>
<p>(ii) Al<sup>3+</sup> + 3e → Al<br />
3F can produce 1 mole (= 27g) Al<br />
∴ To produce 40 g A1 requires<br />
\(\frac{3 \mathrm{F} \times 40}{27}\) = 4.44F</p>
<p>Question 13.<br />
How much electricity is required in coulomb for the oxidation of<br />
(i) 1 mol of H<sub>2</sub>O to O<sub>2</sub><br />
(ii) 1 mol of FeO to Fe<sub>2</sub>O<sub>3</sub>.<br />
Answer:<br />
(i) 2H<sub>2</sub>O → 4H<sup>+</sup> + O<sub>2</sub> + 4e<br />
2F of electricity is required for oxidation of 1 mole of H<sub>2</sub>O<br />
(ii) Fe<sup>2+</sup> → Fe<sup>3+</sup> + e<br />
IF of electricity is required for oxidation of 1 mole FeO</p>
<p>Question 14.<br />
A solution of Ni(NO<sub>3</sub>)<sub>2</sub> is electrolysed between platinum electrodes using a current of 5 amperes for 20 minutes. What mass of Ni is deposited at the cathode?<br />
Answer:<br />
Ni<sup>2+</sup> + 2e<sup>&#8211;</sup> → Ni<br />
2F (2 × 96500 C) can produce 58.7 g of Ni<br />
Q = It = 5 × 20 × 60 =6000C<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72150" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-11.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 11" width="335" height="57" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-11.png 335w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-11-300x51.png 300w" sizes="auto, (max-width: 335px) 100vw, 335px" /></p>
<p>Question 15.<br />
Three electrolytic cells A,B,C containing = 0.439 g of Zn solutions of ZnSO<sub>4</sub>, AgNO<sub>3</sub> and CuSO<sub>4</sub>, respectively are connected in series. A steady current of 1.5 amperes was passed through them until 1.45 g of silver deposited at the cathode of cell B. How long did the current flow? What mass of copper and zinc were deposited?<br />
Answer:<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72151" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-12.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 12" width="175" height="57" /><br />
i.e. 108 g of Ag is deposited by 96487 C<br />
Therefore, 1 .45g of Ag is deposited by<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72153" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-13.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 13" width="251" height="55" /><br />
Given,<br />
Current = 1.5A<br />
\(\frac{1295.43}{1.5}\) S<br />
∴ Time = 863.6S<br />
= 864 S<br />
= 14.40 min<br />
Again,<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72155" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-14.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 14" width="198" height="63" /><br />
i.e. 2 × 96487 C of charge deposit = 63.5 g of Cu<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72157" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-15.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 15" width="163" height="50" /><br />
Therefore, 1295.43 C of charge will deposit = 0.426g of Cu<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72159" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-16.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 16" width="188" height="66" /><br />
i.e. 2 × 96487 C of charge deposit = 65.4 g of Zn<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72161" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-17.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 17" width="147" height="56" /><br />
Therefore, 1295.43 C of charge will deposit = 0.439 g of Zn</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 16.<br />
Predict the products of electrolysis in<br />
each of the following:<br />
(1) An aqueous solution of AgNO<sub>3</sub> with silver electrodes.<br />
(ii) An aqueous solution of AgNO<sub>3</sub> with platinum electrodes.<br />
(iii) A dilute solution of H<sub>2</sub>SO<sub>4</sub> with platinum electrodes.<br />
(iv) An aqueous solution of CuCl<sub>2</sub> with platinum electrodes.<br />
Answer:<br />
(i) At cathode:<br />
The following reduction reactions compete to take place at the cathode<br />
Ag<sup>+</sup>(aq) + e<sup>&#8211;</sup> → Ag(s); E<sup>θ</sup> = 0.80 V<br />
H<sup>+</sup> (aq) + e<sup>&#8211;</sup> → \(\frac { 1 }{ 2 }\) H<sub>2</sub> (g); E<sup>θ</sup> = 0.00V<br />
The reaction with a higher value of E<sub>θ</sub> takes place of the cathode. Therefore, deposition of silver will take place at the cathode.</p>
<p>At anode:<br />
The Ag anode is attacked by NO<sub>3</sub><sup>&#8211;</sup> ions. Therefore, the silver electrode at the anode dissolves in the solution to from Ag<sup>+</sup>.</p>
<p>(ii) At cathode: Same as above<br />
At anode: Anode is not attackable and hence OH<sup>&#8211;</sup> ions have lower discharge potential than NO<sub>3</sub><sup>&#8211;</sup> ions and OH<sup>&#8211;</sup> ions react to give O<sub>2</sub><br />
OH<sup>&#8211;</sup> → OH + e<sup>&#8211;</sup><br />
4OH → 2H<sub>2</sub>O + O<sub>2</sub> (g)<br />
(iii) H<sub>2</sub>SO<sub>4</sub> → 2H<sup>+</sup> + SO<sup>2-</sup><sub>4</sub><br />
HO<sub>2</sub> ⇌ H<sup>+</sup> + OH<sup>&#8211;</sup></p>
<p>At cathode:<br />
2H<sup>+</sup>+ 2e<sup>&#8211;</sup> → H<sub>2</sub><br />
At anode: 4OH<sup>&#8211;</sup> → 2H<sub>2</sub>O + O<sub>2</sub> + 4e<sup>&#8211;</sup><br />
i. e., H<sub>2</sub> will be liberated at cathode and O<sub>2</sub> at anode.</p>
<p>(iv) CuCl<sub>2</sub> → Cu<sup>2+</sup>+2Cl<sup>&#8211;</sup><br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72167" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-18.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 18" width="158" height="30" /><br />
At Cathode: Cu<sup>2+</sup> ions will be reduced in preference to H<sup>+</sup> ions<br />
Cu<sup>2+</sup> + 2e → Cu<br />
At anode: Cl&#8217; ions will be oxidised in preference to OH<sup>&#8211;</sup> ions.<br />
2Cl<sup>&#8211;</sup> → Cl<sub>2</sub> + 2e<sup>&#8211;</sup><br />
i.e., Cu will be deposited on the cathode and<br />
Cl<sub>2</sub> will be liherated at the anode.</p>
<h3 class="n291pb uaxL4e">2nd PUC Chemistry Electrochemistry Additional Questions and Answers</h3>
<p>Question 1.<br />
A solution of sodium chloride is a better<br />
conductor of electricity at a temperature of 50°C than at room temperature. Why?<br />
Answer:<br />
A solution of NaCl shows greater conduction of electricity at a temperature of 50°C than at room temperature because the ionic mobility of a strong electrolyte such as NaCl increases with an increase in temperature.</p>
<p>Question 2.<br />
Give the relationship between molar conductivity and specific conductivity.<br />
Answer:<br />
Molar conductivity and specific conductivity are related to each other by the given equation.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72168" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-19.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 19" width="112" height="50" /><br />
Where,<br />
Δ<sub>m</sub> = Molar conductivity<br />
K = Specific conductivity<br />
C = Molar concentration</p>
<p>Question 3.<br />
Why is it not possible to measure single electrode potential?<br />
Answer:<br />
The process of oxidation or reduction cannot take place alone. However, electrode potential is a relative tendency and can be measured with respect to a reference electrode such as standard hydrogen electrode.</p>
<p>Question 4.<br />
Why is the rusting of iron faster in saline water than in pure water?<br />
Answer:<br />
Strong electrolytes such as sodium chloride are present in saline water. The ions produced from NaCl help in the reduction of oxygen to form water. Hence, the rusting of iron is faster in saline water than in pure water.</p>
<p>Question 5.<br />
What happens Δ<sup>0</sup><sub>m</sub> for weak electrolytes obtained by using Kohlrausch law if the migration of ions is increased to three<br />
Answer:<br />
Δ<sup>0</sup><sub>m</sub> for weak electrolytes obtained by using Kohlrausch law is independent of the migration of ions.</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
<p>Question 6.<br />
Define molar conductivity of a solution.<br />
Answer:<br />
The molar conductivity of a solution at a given concentration is the conductance of volume ‘V’ of a solution containing 1 mole of _ the electrolytic kept between two electrodes with cross sectional area ‘A’ and distance of unit length.<br />
Or,<br />
Δ<sub>m</sub> = \(\frac{\Delta}{1}\) K<br />
Now,<br />
1 = 1 and Δ = V (volume containing 1 mole of the electrolyte)<br />
∴ Δ<sub>m</sub> = KV</p>
<p>Question 7.<br />
What are the factors that affect the conductivity of an ionic (electrolytic) solution?<br />
Answer:<br />
The conductivity of an ionic (electrolytic) solution depends upon the following factors.</p>
<ul>
<li>Temperature</li>
<li>Concentration of electrolyte</li>
<li>Nature of the electrolyte added</li>
<li>Nature of solvent and its viscosity</li>
<li>Size of the ions produced and their solvation.</li>
</ul>
<p>Question 8.<br />
The electrolysis of a salt solution of a metal was carried out by passing a current of 4A for 45 minutes. This resulted in the deposition of 2.977g of the metal. If the atomic mass of the metal is 106.4 g mol<sup>-1</sup>, then calculate the charge present in the metal cation.<br />
Answer:<br />
Let the charge on the metal cation be h i.e. the metal cation is M<sup>+</sup><br />
Accordingly,<br />
M<sup>h+</sup> + 4e<sup>&#8211;</sup> → M<br />
Therefore, a current of h × 96500 coulomb will deposit 106.4 g of metal quantity of charge passed = 10800 coulombs<br />
Now, 10800 coulombs will deposit<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72169" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-20.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 20" width="315" height="160" srcset="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-20.png 315w, https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-20-300x152.png 300w" sizes="auto, (max-width: 315px) 100vw, 315px" /><br />
Hence, the charge present on the metal cation is + 4.</p>
<p>Question 9.<br />
(a) At infinite dilution, the ionic conductance of Ba<sup>2+</sup> and Cl is 121 and 76 ohm1 cm respectively. What will be the equivalent<br />
conductance of BaCl<sub>2</sub> (in ohm<sup>-1</sup> cm<sup>2</sup>) at infinite dilution?<br />
(b) What effect does concentration have on the molar conductivity of a strong electrolyte?<br />
Answer:<br />
(a) The molar conductivity of barium chloride is given by the following equation:<br />
Δ<sup>0</sup><sub>m</sub>(BaCl<sub>2</sub>) = Δ<sup>0</sup>Ba<sup>2+</sup> + 2 Δ<sup>0</sup><sub>Cl-</sub><br />
= 127 + 2 × 76 = 279Ω<sup>-1</sup> cm<sup>2</sup> mol<sup>-1</sup><br />
Δ<sup>0</sup> eq = \(\frac{279}{2}\) Ω<sup>-1</sup>cm<sup>2</sup>Eq<sup>-1</sup><br />
= 139.5 Ω<sup>-1</sup>cm<sup>2</sup> Eq<sup>-1</sup><br />
[∴ Eq.wt. of BaCl2 = \(\frac{1}{2}\) × mol.wt]<br />
Hence the equivalent conductance of BaCl<sub>2</sub> at infinite dilution is 139.5 Ω<sup>-1<sup>cm<sup>2</sup> eq<sup>-1</sup></sup></sup></p>
<p>(b) The molar conductivity of a strong electrolyte decreases with the square root of concentration in linear fashion, as shown below.<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72170" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-21.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 21" width="248" height="199" /></p>
<p>Question 10.<br />
(a) The standard reduction potentials of Fe<sup>3+</sup> | Fe<sup>2+</sup> and I<sup>&#8211;</sup><sup>3</sup> | I<sup>&#8211;</sup>are 0.77 V and 0.54 V respectively for the reaction 2Fe<sup>3+</sup> + 3I<sup>&#8211;</sup> ⇌ 2Fe<sup>2+</sup> + I<sup>&#8211;</sup><sub>3</sub>. Calculate the value of equilibrium constant.<br />
(b) How much charge is required 1 mole of Cu<sup>2+</sup> to Cu<br />
Answer:<br />
(a) The cell may be represented as<br />
<img loading="lazy" decoding="async" class="alignnone size-full wp-image-72171" src="https://ktbssolutions.com/wp-content/uploads/2019/12/2nd-PUC-Chemistry-Question-Bank-Chapter-3-Electrochemistry-22.png" alt="2nd PUC Chemistry Question Bank Chapter 3 Electrochemistry - 22" width="226" height="272" /><br />
Hence, the equilibrium constant for the given cell is 6.025 × 10<sup>7</sup> (b) When copper is reduced, the following reaction takes place Cu<sup>2+</sup> + 2e<sup>&#8211; </sup>→ Cu<br />
Hence, the quantity of charge required for the reduct ion of 1 mole of Cu<sup>2+</sup>= 2F<br />
= 2 × 96500 C = 193000C</p>
<p><img loading="lazy" decoding="async" src="https://ktbssolutions.com/wp-content/uploads/2019/11/KSEEB-Solutions-300x28.png" alt="KSEEB Solutions" width="172" height="16" /></p>
</div>
</div>
</div>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10172</post-id>	</item>
		<item>
		<title>2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane</title>
		<link>https://ktbssolutions.com/2nd-puc-kannada-workbook-answers-chapter-11/</link>
		
		<dc:creator><![CDATA[Prasanna]]></dc:creator>
		<pubDate>Tue, 14 Jul 2026 05:49:18 +0000</pubDate>
				<category><![CDATA[2nd PUC]]></category>
		<guid isPermaLink="false">https://ktbssolutions.com/?p=10231</guid>

					<description><![CDATA[You can Download 2nd PUC Kannada Workbook Answers Pallava Chapter 11 Gade Mathu Vistarane, 2nd PUC Kannada Textbook Answers, Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations. Karnataka 2nd PUC Kannada Workbook Answers Pallava Chapter 11 Gade Mathu Vistarane]]></description>
										<content:encoded><![CDATA[<p>You can Download 2nd PUC Kannada Workbook Answers Pallava Chapter 11 Gade Mathu Vistarane, <a href="https://ktbssolutions.com/2nd-puc-kannada-textbook-answers/">2nd PUC Kannada Textbook Answers</a>, Karnataka State Board Solutions help you to revise complete Syllabus and score more marks in your examinations.</p>
<h2>Karnataka 2nd PUC Kannada Workbook Answers Pallava Chapter 11 Gade Mathu Vistarane</h2>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78067" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-1.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 1" width="582" height="726" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-1.png 582w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-1-240x300.png 240w" sizes="auto, (max-width: 582px) 100vw, 582px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78070" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-2.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 2" width="577" height="722" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-2.png 577w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-2-240x300.png 240w" sizes="auto, (max-width: 577px) 100vw, 577px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78072" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-3.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 3" width="586" height="821" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-3.png 586w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-3-214x300.png 214w" sizes="auto, (max-width: 586px) 100vw, 586px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78075" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-4.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 4" width="589" height="821" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-4.png 589w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-4-215x300.png 215w" sizes="auto, (max-width: 589px) 100vw, 589px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78077" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-5.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 5" width="586" height="786" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-5.png 586w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-5-224x300.png 224w" sizes="auto, (max-width: 586px) 100vw, 586px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78078" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-6.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 6" width="576" height="819" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-6.png 576w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-6-211x300.png 211w" sizes="auto, (max-width: 576px) 100vw, 576px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78090" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-7.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 7" width="581" height="824" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-7.png 581w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-7-212x300.png 212w" sizes="auto, (max-width: 581px) 100vw, 581px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78095" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-8.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 8" width="574" height="790" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-8.png 574w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-8-218x300.png 218w" sizes="auto, (max-width: 574px) 100vw, 574px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78098" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-9.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 9" width="583" height="817" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-9.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-9-214x300.png 214w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78100" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-10.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 10" width="580" height="823" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-10.png 580w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-10-211x300.png 211w" sizes="auto, (max-width: 580px) 100vw, 580px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78102" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-11.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 11" width="583" height="823" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-11.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-11-213x300.png 213w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78104" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-12.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 12" width="584" height="818" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-12.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-12-214x300.png 214w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78107" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-13.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 13" width="577" height="823" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-13.png 577w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-13-210x300.png 210w" sizes="auto, (max-width: 577px) 100vw, 577px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78109" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-14.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 14" width="584" height="759" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-14.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-14-231x300.png 231w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78112" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-15.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 15" width="578" height="824" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-15.png 578w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-15-210x300.png 210w" sizes="auto, (max-width: 578px) 100vw, 578px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78116" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-16.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 16" width="584" height="755" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-16.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-16-232x300.png 232w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78118" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-17.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 17" width="583" height="786" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-17.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-17-223x300.png 223w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78119" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-18.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 18" width="574" height="761" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-18.png 574w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-18-226x300.png 226w" sizes="auto, (max-width: 574px) 100vw, 574px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78126" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-19.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 19" width="583" height="819" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-19.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-19-214x300.png 214w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78128" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-20.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 20" width="583" height="820" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-20.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-20-213x300.png 213w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78129" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-21.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 21" width="582" height="821" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-21.png 582w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-21-213x300.png 213w" sizes="auto, (max-width: 582px) 100vw, 582px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78131" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-22.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 22" width="578" height="821" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-22.png 578w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-22-211x300.png 211w" sizes="auto, (max-width: 578px) 100vw, 578px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78132" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-24.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 24" width="584" height="816" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-24.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-24-215x300.png 215w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78133" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-25.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 25" width="584" height="813" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-25.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-25-215x300.png 215w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78134" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-26.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 26" width="583" height="823" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-26.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-26-213x300.png 213w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78135" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-27.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 27" width="584" height="817" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-27.png 584w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-27-214x300.png 214w" sizes="auto, (max-width: 584px) 100vw, 584px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78137" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-28.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 28" width="568" height="825" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-28.png 568w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-28-207x300.png 207w" sizes="auto, (max-width: 568px) 100vw, 568px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78140" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-29.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 29" width="583" height="819" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-29.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-29-214x300.png 214w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78142" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-30.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 30" width="583" height="822" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-30.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-30-213x300.png 213w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78145" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-31.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 31" width="572" height="823" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-31.png 572w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-31-209x300.png 209w" sizes="auto, (max-width: 572px) 100vw, 572px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78147" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-32.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 32" width="579" height="756" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-32.png 579w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-32-230x300.png 230w" sizes="auto, (max-width: 579px) 100vw, 579px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78150" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-33.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 33" width="579" height="818" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-33.png 579w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-33-212x300.png 212w" sizes="auto, (max-width: 579px) 100vw, 579px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78154" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-34.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 34" width="583" height="822" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-34.png 583w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-34-213x300.png 213w" sizes="auto, (max-width: 583px) 100vw, 583px" /></p>
<p><img loading="lazy" decoding="async" class="alignnone size-full wp-image-78156" src="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-35.png" alt="2nd PUC Kannada Workbook Answers Chapter 11 Gade Mathu Vistarane 35" width="585" height="257" srcset="https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-35.png 585w, https://ktbssolutions.com/wp-content/uploads/2020/11/2nd-PUC-Kannada-Workbook-Answers-Chapter-11-Gade-Mathu-Vistarane-35-300x132.png 300w" sizes="auto, (max-width: 585px) 100vw, 585px" /></p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10231</post-id>	</item>
	</channel>
</rss>

<!--
Performance optimized by W3 Total Cache. Learn more: https://www.boldgrid.com/w3-total-cache/?utm_source=w3tc&utm_medium=footer_comment&utm_campaign=free_plugin

Page Caching using Disk: Enhanced 

Served from: ktbssolutions.com @ 2026-09-11 11:43:06 by W3 Total Cache
-->