The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated. Concept Introduction: The general steps involved in the Gabriel synthesis are as follows. The first step is the reaction of a base with phthalimide to form a salt. The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide . The last step is the hydrolysis to form the desired product or primary amine .

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Answer 1

Question

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

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Answer 2

Question

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

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Answer 3

Question

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

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Answer 4

Question

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

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Answer 5

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

Answer 6

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

Answer 7

Chapter 22, Problem 43P

Interpretation Introduction

Interpretation:

The structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of the potassium salt of phthalimide has to be stated.

Concept Introduction:

The general steps involved in the Gabriel synthesis are as follows.

The first step is the reaction of a base with phthalimide to form a salt.

The next step is the nucleophilic substitution reaction that involves the reaction of a salt of phthalimide ion and the primary alkyl halide.

The last step is the hydrolysis to form the desired product or primary amine.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 22.1 - Prob. 1P Ch. 22.1 - Prob. 2P Ch. 22.1 - Prob. 3P Ch. 22.2 - Prob. 4P Ch. 22.4 - Prob. 5P Ch. 22.4 - Prob. 6P Ch. 22.4 - Prob. 7P Ch. 22.4 - Prob. 8P Ch. 22.4 - Prob. 9P Ch. 22.7 - Prob. 10P

Solution Summary: The author explains the structure of the phthalimide derivative formed by the reaction of given dihaloalkanes with one equivalent of potassium salt.

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Chapter 22 Solutions