(a) Interpretation: The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated. Concept introduction: Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α , β − unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

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Answer 1

Question

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

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Answer 2

Question

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

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Answer 3

Question

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

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Answer 4

Question

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

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Answer 5

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 6

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 7

Chapter 22, Problem 22.47P

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the reaction of a methyl amine with methyl arcylate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the reaction of phenyl thiolate with α,β− unsaturated carbonyl compound is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the reaction of a dimethyl amine with diethyl maleate is to be stated.

Concept introduction:

Conjugate addition reactions are those reactions in which a nucleophile attacks at the double bond of an α,β− unsaturated carbonyl compound. This reaction is thermodynamically stable. The nucleophile attacks at the double bond because the intermediate formed is resonance stabilized.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 22 - Prob. 22.1P Ch. 22 - Prob. 22.2P Ch. 22 - Prob. 22.3P Ch. 22 - Prob. 22.4P Ch. 22 - Prob. 22.5P Ch. 22 - Prob. 22.6P Ch. 22 - Prob. 22.7P Ch. 22 - Prob. 22.8P Ch. 22 - Prob. 22.9P Ch. 22 - Prob. 22.10P

Solution Summary: The author explains the curved-arrow mechanism for the reaction of a methyl amine with an unsaturated carbonyl compound.

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