Organic Chemistry, Ebook And Single-course Homework Access
Organic Chemistry, Ebook And Single-course Homework Access
6th Edition
ISBN: 9781319085841
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 21, Problem 21.10P
Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the hydrolysis of the N-methylbenzamide in acidic solution is to be stated.

Concept introduction:

The hydrolysis is the reaction in which a compound is broken down using the molecule of water. The hydrolysis reactions are generally catalyzed by acids and bases. The hydrolysis of the carboxylic derivatives produces carboxylic acids.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the hydrolysis of the N-methylbenzamide in basic solution is to be stated.

Concept introduction:

The hydrolysis is the reaction in which a compound is broken down from one bond using the molecule of water. The hydrolysis reactions are generally catalyzed by acids and bases. The hydrolysis of the carboxylic derivatives produces carboxylic acids.

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Part II. two unbranched ketone have molecular formulla (C8H100). El-ms showed that both of them have a molecular ion peak at m/2 =128. However ketone (A) has a fragment peak at m/2 = 99 and 72 while ketone (B) snowed a fragment peak at m/2 = 113 and 58. 9) Propose the most plausible structures for both ketones b) Explain how you arrived at your conclusion by drawing the Structures of the distinguishing fragments for each ketone, including their fragmentation mechanisms.
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