The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated. Concept Introduction: An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage ( N = N ) . The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

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Answer 1

Question

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

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Answer 2

Question

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

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Answer 3

Question

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

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Answer 4

Question

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

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Answer 5

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

Answer 6

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

Answer 7

Chapter 18.20, Problem 36P

Interpretation Introduction

Interpretation:

The explanation for the formation of nitrosamine from secondary amine rather than a diazonium ion when it reacts with nitrosonium ion is to be stated.

Concept Introduction:

An electrophilic substitution reaction between highly activated aromatic ring and arene-diazonium ion electrophile leads to the formation of azo linkage (N=N). The reaction is highly favorable when electron withdrawing group is present on arene-diazonium ion and electron donating group on aromatic ring.

Answer 8

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Answer 11

Ch. 18.1 - Draw the structure for each of the following: a....Ch. 18.3 - Why does hydration inactivate FeBr3?Ch. 18.6 - Prob. 4P Ch. 18.7 - What is the major product of a Friedel-Crafts...Ch. 18.9 - Describe two ways to prepare each of the following...Ch. 18.10 - Prob. 7P Ch. 18.11 - Name the following:Ch. 18.11 - Draw a structure for each of the following: a....Ch. 18.11 - Draw the structure for each of the following: a....Ch. 18.11 - Correct the following incorrect names: a....

Solution Summary: The author explains the mechanism of formation of nitrosamine from secondary amine rather than a diazonium ion.

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