The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained. Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows: Tertiary > > secondary > primary

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Answer 1

Question

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

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Answer 2

Question

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

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Answer 3

Question

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

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Answer 4

Question

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

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Answer 5

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

Answer 6

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

Answer 7

Chapter 7.1, Problem 7.1E

Interpretation Introduction

Interpretation: The reason behind compound A completely stable in ethanol while B converted into another compound rapidly should be explained.

Concept introduction: The haloalkanes react with various solvents such as water, ethanol to give substituted products that have halide replaced by nucleophilic part of solvent. Such reactions are termed solvolysis. The experimental order of reactive for three types of halides towards solvolysis is as follows:

Tertiary>> secondary>primary

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 7.1 - Prob. 7.1E Ch. 7.2 - Prob. 7.2E Ch. 7.3 - Prob. 7.3E Ch. 7.3 - Prob. 7.5TIY Ch. 7.4 - Prob. 7.7TIY Ch. 7.5 - Prob. 7.9TIY Ch. 7.6 - Prob. 7.10E Ch. 7.7 - Prob. 7.11E Ch. 7.7 - Prob. 7.12E Ch. 7.7 - Prob. 7.13E

Solution Summary: The author explains the reason behind compound A completely stable in ethanol while B converted into another compound rapidly. The experimental order of reactive for three types of halides is dependent upon the structure of the substrates.

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