ORGANIC CHEMISTRY (LOOSELEAF)
ORGANIC CHEMISTRY (LOOSELEAF)
6th Edition
ISBN: 9781260475630
Author: SMITH
Publisher: MCG
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Chapter 21.9, Problem 24P
Interpretation Introduction

(a)

Interpretation: The alkyl halide needed to prepare carboxylic acid by the malonic ester synthesis is to be predicted.

Concept introduction: The α hydrogen attached to the diester is acidic in nature and on heating diester followed by hydrolysis gives β- diacid which loses CO2 to give carboxylic acid. The formed acid has components of both alkyl halide and malonic ester.

Interpretation Introduction

(b)

Interpretation: The alkyl halides needed to prepare carboxylic acid by the malonic ester syntheses are to be predicted.

Concept introduction: The α hydrogen attached to the diester is acidic in nature and on heating diester followed by hydrolysis gives β- diacid which loses CO2 to give carboxylic acid. The formed acid has components of both alkyl halide and malonic ester.

Interpretation Introduction

(c)

Interpretation: The alkyl halides needed to prepare carboxylic acid by the malonic ester syntheses are to be predicted.

Concept introduction: The α hydrogen attached to the diester is acidic in nature and on heating diester followed by hydrolysis gives β- diacid which loses CO2 to give carboxylic acid. The formed acid has components of both alkyl halide and malonic ester.

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Chapter 21 Solutions

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