ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
9th Edition
ISBN: 9780134645704
Author: WADE AND SIMEK
Publisher: PEARSON
Question
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Chapter 21, Problem 21.47SP

(a)

Interpretation Introduction

Interpretation:

The product of saponification of the given ester has to be predicted.

Concept introduction:

The formation of ester molecule from carboxylic acid and alcohol is known as esterification. The reverse of esterification is known as hydrolysis or saponification.

(b)

Interpretation Introduction

Interpretation:

The product of saponification of the given ester is to be predicted.

Concept introduction:

The formation of ester molecule from carboxylic acid and alcohol is known as esterification. The reverse of esterification is known as hydrolysis or saponification.

(c)

Interpretation Introduction

Interpretation:

The product of saponification of the given ester is to be predicted.

Concept introduction:

The formation of ester molecule from carboxylic acid and alcohol is known as esterification. The reverse of esterification is known as hydrolysis or saponification.

(d)

Interpretation Introduction

Interpretation:

The product of saponification of the given ester is to be predicted.

Concept introduction:

The formation of ester molecule from carboxylic acid and alcohol is known as esterification. The reverse of esterification is known as hydrolysis or saponification.

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Students have asked these similar questions
What are steps in acid-catalyzed ester hydrolysis ?
CH,CH,COOH Carboxylic Acid SOCI₂ H₂O Acid anhydride CH₂CH₂COO-Na Acid chloride CH,OH Ester CH,CH,NH, Amide
Why are carbonyl compounds considered weakly acidic? Would you expect carbonyl compounds to be more acidic than alkanes? Explain.

Chapter 21 Solutions

ORGANIC CHEMISTRY

Ch. 21.7C - Prob. 21.20PCh. 21.7C - Prob. 21.21PCh. 21.7D - Prob. 21.22PCh. 21.7D - The mechanism for acidic hydrolysis of a nitrile...Ch. 21.8A - Prob. 21.24PCh. 21.8C - Prob. 21.25PCh. 21.9 - Prob. 21.26PCh. 21.9 - Prob. 21.27PCh. 21.9 - Prob. 21.28PCh. 21.10 - Draw a mechanism for the acylation of anisole by...Ch. 21.10 - Prob. 21.30PCh. 21.11 - Prob. 21.31PCh. 21.11 - Prob. 21.32PCh. 21.12 - Problem 21-33 Propose a mechanism for the...Ch. 21.12 - Suggest the most appropriate reagent for each...Ch. 21.12 - Show how you would synthesize each compound,...Ch. 21.13 - Prob. 21.36PCh. 21.13 - Prob. 21.37PCh. 21.14 - Prob. 21.38PCh. 21.14 - Prob. 21.39PCh. 21.16 - Prob. 21.40PCh. 21.16 - Prob. 21.41PCh. 21 - Prob. 21.42SPCh. 21 - Give appropriate names for the following...Ch. 21 - Predict the major products formed when benzoyl...Ch. 21 - Predict the products of the following reactions....Ch. 21 - Prob. 21.46SPCh. 21 - Prob. 21.47SPCh. 21 - Prob. 21.48SPCh. 21 - Propose mechanisms for the following reactions.Ch. 21 - Prob. 21.51SPCh. 21 - An ether extraction of nutmeg gives large...Ch. 21 - Prob. 21.53SPCh. 21 - Show how you would accomplish the following...Ch. 21 - Prob. 21.55SPCh. 21 - Prob. 21.56SPCh. 21 - Prob. 21.57SPCh. 21 - Prob. 21.58SPCh. 21 - Prob. 21.59SPCh. 21 - Explain this curious result. What does this...Ch. 21 - Prob. 21.61SPCh. 21 - Prob. 21.62SPCh. 21 - Prob. 21.63SPCh. 21 - A chemist was called to an abandoned aspirin...Ch. 21 - Prob. 21.67SPCh. 21 - The IR spectrum, 13ONTVTR spectrum, and 1HNMR...Ch. 21 - Prob. 21.69SPCh. 21 - Prob. 21.70SPCh. 21 - Prob. 21.71SP
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