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.

Question

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Answer 1

Question

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.

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Answer 2

Question

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.

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Answer 3

Question

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.

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Answer 4

Question

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.

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Answer 5

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.

Answer 6

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.

Answer 7

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.

Answer 8

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.

Answer 9

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.

Answer 10

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.

Answer 11

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.

Answer 12

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.

Answer 13

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.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. 16.1 - Give two names for each of the following:Ch. 16.1 - Prob. 2P Ch. 16.1 - Name the following:Ch. 16.2 - Prob. 4P Ch. 16.4 - What products are formed when the following...Ch. 16.4 - We saw on the previous page that...Ch. 16.4 - a. How many stereoisomers are obtained from the...Ch. 16.4 - Prob. 9P Ch. 16.4 - Write the mechanism for the reaction of acetyl...Ch. 16.4 - Prob. 11P

Solution Summary: The author explains that the carbonyl group is electrophilic and undergoes nucleophilic addition reactions.

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Chapter 16 Solutions