ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
6th Edition
ISBN: 9781264382545
Author: SMITH
Publisher: MCG CUSTOM
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Chapter 22, Problem 33P
Interpretation Introduction

(a)

Interpretation: The product that is formed by the intramolecular aldol reaction of the given dicarbonyl compound followed by dehydration is to be drawn.

Concept introduction: The aldol reaction that takes place within the same molecule in the presence of strong base is known as intramolecular aldol reactions. This reaction generally takes place within the dicarbonyl compounds in which one carbonyl group forms the enolate ion that acts as a nucleophile and the carbonyl carbon of the second carbonyl group acts as an electrophile.

Interpretation Introduction

(b)

Interpretation: The product that is formed by the intramolecular aldol reaction of the given dicarbonyl compound followed by dehydration is to be drawn.

Concept introduction: The aldol reaction that takes place within the same molecule in the presence of strong base is known as intramolecular aldol reactions. This reaction generally takes place within the dicarbonyl compounds in which one carbonyl group forms the enolate ion that acts as a nucleophile and the carbonyl carbon of the second carbonyl group acts as an electrophile.

Interpretation Introduction

(c)

Interpretation: The product that is formed by the intramolecular aldol reaction of the given dicarbonyl compound followed by dehydration is to be drawn.

Concept introduction: The aldol reaction that takes place within the same molecule in the presence of strong base is known as intramolecular aldol reactions. This reaction generally takes place within the dicarbonyl compounds in which one carbonyl group forms the enolate ion that acts as a nucleophile and the carbonyl carbon of the second carbonyl group acts as an electrophile.

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Chapter 22 Solutions

ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS

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