A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated. Concept introduction: The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Question

Want to see the full answer?

Answer 1

Question

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Please help me with number 1-3. Thank you so much.

Draw the major product of this reaction ingnore the inorganic byproducts. 1. NaOCH2CH3 at 25 C 2. PhCH2Br (1 eq)

At 90ºC the vapor pressure of ortho-xylene is 20 kPa and that of meta-xylene is 18 kPa. What is the composition of the vapor in equilibrium with a mixture in which the mole fraction of o-xylene is 0.60?

Answer 2

Question

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Answer 6

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Answer 7

Chapter 21.7D, Problem 21.22P

Interpretation Introduction

Interpretation:

A mechanism corresponding to the basic hydrolysis of benzonitrile to the benzoate ion and ammonia is to be stated.

Concept introduction:

The basic hydrolysis of benzonitrile to the benzoate ion and ammonia comprises three steps. The first step is the addition of hydroxide ion to the carbon of cyano group. The second step is formation of enol tautomer of amide. The third step is the tautomerism (removal and displacement of a proton).

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 11

Ch. 21.2F - Name the following carboxylic acid derivatives,...Ch. 21.4A - Prob. 21.2P Ch. 21.4A - Prob. 21.3P Ch. 21.4A - Prob. 21.4P Ch. 21.5C - Prob. 21.7P Ch. 21.6 - When ethyl 4-hydroxybutyrate is heated in the...Ch. 21.6 - Propose a mechanism for the following ring-opening...Ch. 21.6 - Prob. 21.15P Ch. 21.7B - Prob. 21.16P Ch. 21.7C - Prob. 21.19P

Want to see the full answer?

Chapter 21 Solutions