The given allyl disulfide is to be synthesised from allyl bromide. Concept introduction: Thiols and disulphides undergo oxidation-reduction reaction during their interconversion. This can be depicted as: Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

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Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

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Answer 2

Question

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

Expert Solution & Answer

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Answer 3

Question

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

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Answer 4

Question

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

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Answer 5

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

Answer 6

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

Answer 7

Chapter F, Problem 3PP

Interpretation Introduction

Interpretation:

The given allyl disulfide is to be synthesised from allyl bromide.

Concept introduction:

Thiols and disulphides undergo oxidation-reduction reaction during their interconversion.

This can be depicted as:

Sulphur ylide acts as a nucleophile and attacks the carbonyl carbon of aldehydes and ketones. In case of reactions with halide compounds it forms an ionic salt.

Answer 8

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Answer 11

Ch. F - Practice Problem F.1 Show how you might use a...Ch. F - Prob. 2PP Ch. F - Prob. 3PP Ch. F - Prob. 4PP

Solution Summary: The author explains that allyl disulfide is synthesized from allyl bromide, which is a nucleophile and attacks aldehydes and ketones.

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Chapter F Solutions