Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 17, Problem 17.37P

(a)

Interpretation Introduction

Interpretation: The name of carboxylic acid and alcohol has to be determined, from which the given eseter is derived.

Concept introduction:

Esters encompass a large family of organic compound with broad application in various fields of science and technology.

In Fischer esterification, a carboxylic acid is reacted with an alcohol in the presence of an acid catalyst, such as concentrated sulfuroc acid.

Esters can be simply represented as,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  1

Fischer esterification can be represented as follows,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  2

The splitting of an ester into the component acid and alcohol is known as ester hydrolysis.

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  3

(b)

Interpretation Introduction

Interpretation: The name of carboxylic acid and alcohol has to be determined, from which the given eseter is derived.

Concept introduction:

Esters encompass a large family of organic compound with broad application in various fields of science and technology.

In Fischer esterification, a carboxylic acid is reacted with an alcohol in the presence of an acid catalyst, such as concentrated sulfuroc acid.

Esters can be simply represented as,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  4

Fischer esterification can be represented as follows,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  5

The splitting of an ester into the component acid and alcohol is known as ester hydrolysis.

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  6

(c)

Interpretation Introduction

Interpretation: The name of carboxylic acid and alcohol has to be determined, from which the given eseter is derived.

Concept introduction:

Esters encompass a large family of organic compound with broad application in various fields of science and technology.

In Fischer esterification, a carboxylic acid is reacted with an alcohol in the presence of an acid catalyst, such as concentrated sulfuroc acid.

Esters can be simply represented as,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  7

Fischer esterification can be represented as follows,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  8

The splitting of an ester into the component acid and alcohol is known as ester hydrolysis.

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  9

(d)

Interpretation Introduction

Interpretation: The name of carboxylic acid and alcohol has to be determined, from which the given eseter is derived.

Concept introduction:

Esters encompass a large family of organic compound with broad application in various fields of science and technology.

In Fischer esterification, a carboxylic acid is reacted with an alcohol in the presence of an acid catalyst, such as concentrated sulfuroc acid.

Esters can be simply represented as,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  10

Fischer esterification can be represented as follows,

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  11

The splitting of an ester into the component acid and alcohol is known as ester hydrolysis.

Organic Chemistry, Chapter 17, Problem 17.37P , additional homework tip  12

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Convert the structure below to a skeletal drawing. H C 010 H. I C 010 C=O C H C. H

Chapter 17 Solutions

Organic Chemistry

Ch. 17 - Write the IUPAC name of each compound, showing...Ch. 17 - Prob. 17.8PCh. 17 - Prob. 17.9PCh. 17 - Prob. 17.10PCh. 17 - Prob. 17.11PCh. 17 - Prob. 17.12PCh. 17 - Prob. 17.13PCh. 17 - On a cyclohexane ring, an axial carboxyl group has...Ch. 17 - Prob. 17.15PCh. 17 - Prob. 17.16PCh. 17 - Prob. 17.17PCh. 17 - Complete each reaction.Ch. 17 - Prob. 17.19PCh. 17 - Prob. 17.20PCh. 17 - Prob. 17.21PCh. 17 - Show the reagents and experimental conditions...Ch. 17 - Prob. 17.23PCh. 17 - Prob. 17.24PCh. 17 - Prob. 17.25PCh. 17 - In each set, assign the acid its appropriate pKa.Ch. 17 - Low-molecular-weight dicarboxylic acids normally...Ch. 17 - Complete the following acid-base reactions. (a)...Ch. 17 - Prob. 17.29PCh. 17 - Prob. 17.30PCh. 17 - Excess ascorbic acid is excreted in the urine, the...Ch. 17 - Give the expected organic product when...Ch. 17 - Show how to convert trans-3-phenyl-2-propenoic...Ch. 17 - Show how to convert 3-oxobutanoic acid...Ch. 17 - Prob. 17.35PCh. 17 - Prob. 17.36PCh. 17 - Prob. 17.37PCh. 17 - When 4-hydroxybutanoic acid is treated with an...Ch. 17 - Fischer esterification cannot be used to prepare...Ch. 17 - Draw the product formed on thermal decarboxylation...Ch. 17 - Prob. 17.41PCh. 17 - Show how cyclohexanecarboxylic acid could be...Ch. 17 - Prob. 17.43PCh. 17 - Prob. 17.44PCh. 17 - Prob. 17.45PCh. 17 - Write the products of the following sequences of...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Using your reaction roadmaps as a guide, show how...Ch. 17 - Prob. 17.51PCh. 17 - Complete the following Fischer esterification...Ch. 17 - Prob. 17.53P
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