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		<title>CHM305 : ORGANIC CHEMISTRY III (2014)</title>
		<link>https://campusflava.com/blog/chm305-organic-chemistry-iii-2014/</link>
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		<dc:creator><![CDATA[Admin_Louis]]></dc:creator>
		<pubDate>Tue, 05 Jan 2021 13:01:36 +0000</pubDate>
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		<category><![CDATA[ORGANIC CHEMISTRY III]]></category>
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					<description><![CDATA[<p>NATIONAL OPEN UNIVERSITY OF NIGERIA 14/16 AHMADU BELLO WAY, VICTORIA ISLAND, LAGOS SCHOOL OF SCIENCE AND TECHNOLOGY MARCH/APRIL 2014 EXAMINATION COURSE CODE: CHM 305 COURSE TITLE: ORGANIC CHEMISTRY III TIME ALLOWED: 2 1/2 HOURS INSTRUCTION: ANSWER QUESTION 1 AND ANY OTHER FOUR QUESTIONS 1a) State the condition(s) for the following reaction i) ii) iii) iv) [&#8230;]</p>
The post <a href="https://campusflava.com/blog/chm305-organic-chemistry-iii-2014/">CHM305 : ORGANIC CHEMISTRY III (2014)</a> first appeared on <a href="https://campusflava.com">Campusflava</a>.]]></description>
										<content:encoded><![CDATA[<p><strong>NATIONAL OPEN UNIVERSITY OF NIGERIA</strong></p>
<p><strong>14/16 AHMADU BELLO WAY, VICTORIA ISLAND, LAGOS</strong></p>
<p><strong>SCHOOL OF SCIENCE AND TECHNOLOGY</strong></p>
<p><strong>MARCH/APRIL 2014 EXAMINATION</strong></p>
<p><strong>COURSE CODE: CHM 305</strong></p>
<p><strong>COURSE TITLE: ORGANIC CHEMISTRY III</strong></p>
<p><strong>TIME ALLOWED: 2 1/2 HOURS</strong></p>
<p><strong> INSTRUCTION:</strong> <strong>ANSWER QUESTION 1 AND ANY OTHER FOUR QUESTIONS</strong></p>
<p>1a) State the condition(s) for the following reaction</p>
<p>i)</p>
<p>ii)</p>
<p>iii)</p>
<p>iv)</p>
<p>State the product(s) formed from the following reactions</p>
<p>v)</p>
<p>vi)</p>
<p>vii)</p>
<p>2a) Differentiate between isomerism and metamerism.</p>
<p>2b) Discuss the general methods of preparing Esters.</p>
<p>2c) Explain transesterification.</p>
<p>3a) Explain the physical properties of aldehydes and ketones.</p>
<p>3b) Discuss the reaction that occurs when ozone is bubbled through a solution of an alkene in 1,1,1-</p>
<p>trichloromethane followed by hydrolysis in the presence of zinc and ethanoic acid.</p>
<p>4a) Discuss the formation of β-Keto esters.</p>
<p>4b) Explain 1,4-nucleophilic Addition using specific reaction.</p>
<p>5a) Classify Heterocyclic Compounds into their main categories.</p>
<p>5b) Discuss the reaction of Thiophene with Organometallic compounds.</p>
<p>5c) State the test for Thiophene.</p>
<p>6a) Discuss the preparation of Pyridine from Pentamethylenediamine hydrochloric acid.</p>
<p>6b) Highlight the physical properties of Pyridine.</p>
<p>6c) Discuss the Nucleophilic substitution of Pyridine.</p>
<p>7a) State the physical characteristics of dicarboxylic acids</p>
<p>7b) Discuss the Preparation of Malonic Esters.</p>
<p><strong>For the 2015 &#8211; <strong>till date past questions</strong> for this course <strong><a href="https://campusflava.com/past-questions/">CLICK HERE</a></strong></strong></p>
<p><strong>Contact me for your TMA, GST302 Business plan writeup, Project Writeup and also get your <a href="https://campusflava.com/blog/what-is-exam-summary/">Exam Summary</a> for this course.</strong></p>The post <a href="https://campusflava.com/blog/chm305-organic-chemistry-iii-2014/">CHM305 : ORGANIC CHEMISTRY III (2014)</a> first appeared on <a href="https://campusflava.com">Campusflava</a>.]]></content:encoded>
					
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