The product of the sequence of reactions shown is to be predicted. Concept introduction: This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp 3 - Carbon of the CH 2 -Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

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Answer 1

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Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

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Answer 2

Question

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

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Answer 3

Question

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

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Answer 4

Question

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

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Answer 5

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

Answer 6

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

Answer 7

Chapter 20, Problem 20.6P

Interpretation Introduction

Interpretation:

The product of the sequence of reactions shown is to be predicted.

Concept introduction:

This is a Gabriel synthesis, which yields a primary amine from an alkyl halide and gives phthalate as a by-product. The aromatic C-Br is inert to these reaction conditions. The sp³- Carbon of the CH2-Br bond is the electrophilic C atom susceptible to nucleophilic attack. The Gabriel synthesis produces only the intended primary amine.

Answer 8

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Answer 11

Ch. 20 - Prob. 20.1P Ch. 20 - Prob. 20.2P Ch. 20 - Prob. 20.3P Ch. 20 - Prob. 20.4P Ch. 20 - Prob. 20.5P Ch. 20 - Prob. 20.6P Ch. 20 - Prob. 20.7P Ch. 20 - Prob. 20.8P Ch. 20 - Prob. 20.9P Ch. 20 - Prob. 20.10P

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