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 20.8, Problem 13P
Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

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