Chapter 16, Problem 73P

a.

Interpretation Introduction

Interpretation:

To write the products of the given reactions.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature, therefore it undergoes nucleophilic addition reactions.

For example carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group. Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

b.

Interpretation Introduction

Interpretation:

To write the products of the given reactions.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature, therefore it undergoes nucleophilic addition reactions.

For example carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group. Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

c.

Interpretation Introduction

Interpretation:

To write the products of the given reactions.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature, therefore it undergoes nucleophilic addition reactions.

For example carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group. Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.

d.

Interpretation Introduction

Interpretation:

To write the products of the given reactions.

Concept introduction:

So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature, therefore it undergoes nucleophilic addition reactions.

For example carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group. Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.