Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 20.7, Problem 11P
Interpretation Introduction

(a)

Interpretation: The products formed from the treatment of benzoyl chloride (C6H5COCl) with H2O, pyridine are to be drawn.

Concept introduction: The nucleophilic acyl substitution of acid chlorides involves two steps; that is the addition of nucleophile to carbonyl group, followed by the elimination of leaving group to give nucleophilic substitution product.

Interpretation Introduction

(b)

Interpretation: The products formed from the treatment of benzoyl chloride (C6H5COCl) with CH3COO are to be drawn.

Concept introduction: The nucleophilic acyl substitution of acid chlorides involves two steps; that is the addition of nucleophile to carbonyl group, followed by the elimination of leaving group to give nucleophilic substitution product.

Interpretation Introduction

(c)

Interpretation: The products formed from the treatment of benzoyl chloride (C6H5COCl) with NH3 (excess) are to be drawn.

Concept introduction: The nucleophilic acyl substitution of acid chlorides involves two steps; that is the addition of nucleophile to carbonyl group, followed by the elimination of leaving group to give nucleophilic substitution product.

Interpretation Introduction

(d)

Interpretation: The products formed from the treatment of benzoyl chloride (C6H5COCl) with (CH3)2NH (excess) are to be drawn.

Concept introduction: The nucleophilic acyl substitution of acid chlorides involves two steps; that is the addition of nucleophile to carbonyl group, followed by the elimination of leaving group to give nucleophilic substitution product.

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