a) Interpretation: To describe how the amines to be prepared using reductive amination reactions.

Question

Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. p-bromoaniline

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

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Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. p-bromoaniline

Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. c) m-bromoaniline

Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. (c) m-bromoaniline (d) m-aminobenzoic acid

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

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Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

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Answer 5

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Answer 6

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Answer 7

Chapter 24.6, Problem 11P

Interpretation Introduction

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Answer 8

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Answer 9

Interpretation Introduction

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

Answer 10

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Answer 11

Interpretation Introduction

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Answer 12

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Answer 13

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Answer 23

Ch. 24.1 - Name the following compounds:Ch. 24.1 - Prob. 2P Ch. 24.1 - Prob. 3P Ch. 24.3 - Prob. 4P Ch. 24.3 - The benzylammonium ion (C6H5CH2NH3+) has pKa =...Ch. 24.4 - Prob. 6P Ch. 24.5 - Prob. 7P Ch. 24.6 - Prob. 8P Ch. 24.6 - Prob. 9P Ch. 24.6 - Show two methods for the synthesis of dopamine, a...

a) Interpretation: To describe how the amines to be prepared using reductive amination reactions.

Solution Summary: The author explains how a retrosynthetic strategy looks at the target molecule and works backwards to arrive at starting materials.

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

Chapter 24 Solutions

a) Interpretation: To describe how the amines to be prepared using reductive amination reactions.

Solution Summary: The author explains how a retrosynthetic strategy looks at the target molecule and works backwards to arrive at starting materials.

a) Interpretation: To describe how the amines to be prepared using reductive amination reactions.

b) Interpretation: To describe how the amines to be prepared using reductive amination reactions

c) Interpretation: To describe how the amines to be prepared using reductive amination reactions.

Chapter 24 Solutions

a)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.

b)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions

c)

Interpretation:

To describe how the amines to be prepared using reductive amination reactions.