The given synthesis is to be carried out. Concept introduction: Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH - 2 group; therefore further undo the substitution and diazotisation to get the NH - 2 group at the place of Br . The synthesis is then carried out with necessary reagents.

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Question

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

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Answer 2

Question

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

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Answer 3

Question

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

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Answer 4

Question

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

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Answer 5

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

Answer 6

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

Answer 7

Chapter 23, Problem 23.84P

Interpretation Introduction

Interpretation:

The given synthesis is to be carried out.

Concept introduction:

Retro synthesis is carried out. If we see the target compound, it is a bromination product. So we undo the bromination. Starting molecule has NH-2 group; therefore further undo the substitution and diazotisation to get the NH-2 group at the place of Br. The synthesis is then carried out with necessary reagents.

Answer 8

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Answer 11

Ch. 23 - Prob. 23.1P Ch. 23 - Prob. 23.2P Ch. 23 - Prob. 23.3P Ch. 23 - Prob. 23.4P Ch. 23 - Prob. 23.5P Ch. 23 - Prob. 23.6P Ch. 23 - Prob. 23.7P Ch. 23 - Prob. 23.8P Ch. 23 - Prob. 23.9P Ch. 23 - Prob. 23.10P

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Chapter 23 Solutions