Organic Chemistry, Loose-leaf Version
Organic Chemistry, Loose-leaf Version
8th Edition
ISBN: 9781305865549
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
Question
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Chapter 17, Problem 17.51P

(a)

Interpretation Introduction

Interpretation:

The product has to be written for the reaction involving excess CH2N2 and methanol.

Concept Introduction:

Esters can be simply represented as,

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  1

Carboxylic acids can be converted to their methyl esters by adding an ether/alcoholic solution of diazomethane.

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  2

(b)

Interpretation Introduction

Interpretation:

The product has to be written for the reaction involving excess CH2N2 and methanol.

Concept Introduction:

Esters can be simply represented as,

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  3

Carboxylic acids can be converted to their methyl esters by adding an ether/alcoholic solution of diazomethane.

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  4

(c)

Interpretation Introduction

Interpretation:

The product has to be written for the reaction involving excess CH2N2 and methanol.

Concept Introduction:

Esters can be simply represented as,

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  5

Carboxylic acids can be converted to their methyl esters by adding an ether/alcoholic solution of diazomethane.

Organic Chemistry, Loose-leaf Version, Chapter 17, Problem 17.51P , additional homework tip  6

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Chapter 17 Solutions

Organic Chemistry, Loose-leaf Version

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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