Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119338352
Author: Klein
Publisher: WILEY
Question
Book Icon
Chapter 22.10, Problem 25CC

 (a)

Interpretation Introduction

 Interpretation: The formation of the products has to be found via an azo coupling reaction by treating with NaNO2 and HCl.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

Organic Chemistry, Chapter 22.10, Problem 25CC , additional homework tip  1

To find: Get the product via an azo coupling reaction by treating the compound (a) with NaNO2 and HCl

Find the nature of the given amine (a)

(b)

Interpretation Introduction

Interpretation: The formation of the products has to be found via an azo coupling reaction by treating with NaNO2 and HCl.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

Organic Chemistry, Chapter 22.10, Problem 25CC , additional homework tip  2

To find: Get the product via an azo coupling reaction by treating the compound (b) with NaNO2 and HCl

Find the nature of the given amine (b)

(c)

Interpretation Introduction

Interpretation: The formation of the products has to be found via an azo coupling reaction by treating with NaNO2 and HCl.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

Organic Chemistry, Chapter 22.10, Problem 25CC , additional homework tip  3

To find: Get the product via an azo coupling reaction by treating the compound (c) with NaNO2 and HCl

Find the nature of the given amine (c)

(d)

Interpretation Introduction

Interpretation: The formation of the products has to be found via an azo coupling reaction by treating with NaNO2 and HCl.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

Organic Chemistry, Chapter 22.10, Problem 25CC , additional homework tip  4

To find: Get the product via an azo coupling reaction by treating the compound (d) with NaNO2 and HCl

Find the nature of the given amine (d)

Blurred answer
Students have asked these similar questions
6 D 2. (1 pt) Limonene can be isolated by performing steam distillation of orange peel. Could you have performed this experiment using hexane instead of water? Explain. 3. (2 pts) Using GCMS results, analyze and discuss the purity of the Limonene obtained from the steam distillation of orange peel.
Part III. Arrange the following carbons (in blue) in order of increasing chemical shift. HO B NH 2 A CI
6. Choose the compound that will produce the spectrum below and assign the signals as carbonyl, aryl, or alkyl. 100 ō (ppm) 50 0 7. 200 150 Assign all of the protons on the spectrum below. 8. A B 4 E C 3 ō (ppm) 2 1 0 Choose the compound that will produce the spectrum below and assign the signals to the corresponding protons. OH 6 OH 3 2 1 0 4 ō (ppm)

Chapter 22 Solutions

Organic Chemistry

Ch. 22.4 - Prob. 10CCCh. 22.4 - Prob. 11CCCh. 22.5 - Prob. 2LTSCh. 22.5 - Prob. 12PTSCh. 22.5 - Prob. 13ATSCh. 22.6 - Prob. 3LTSCh. 22.6 - Prob. 14PTSCh. 22.6 - Prob. 15ATSCh. 22.7 - Prob. 4LTSCh. 22.7 - Prob. 16PTSCh. 22.7 - Prob. 17PTSCh. 22.7 - Prob. 18PTSCh. 22.7 - Prob. 19ATSCh. 22.8 - Prob. 20CCCh. 22.8 - Prob. 21CCCh. 22.8 - Prob. 22CCCh. 22.9 - Prob. 5LTSCh. 22.9 - Prob. 23PTSCh. 22.9 - Prob. 24ATSCh. 22.10 - Prob. 25CCCh. 22.11 - Prob. 26CCCh. 22.11 - Prob. 6LTSCh. 22.11 - Prob. 27PTSCh. 22.11 - Prob. 28ATSCh. 22.12 - Prob. 29CCCh. 22.12 - Prob. 30CCCh. 22.13 - Prob. 31CCCh. 22.13 - Prob. 32CCCh. 22 - Prob. 33PPCh. 22 - Prob. 34PPCh. 22 - Prob. 35PPCh. 22 - Prob. 36PPCh. 22 - Prob. 37PPCh. 22 - Prob. 38PPCh. 22 - Prob. 39PPCh. 22 - Prob. 40PPCh. 22 - Prob. 41PPCh. 22 - Prob. 42PPCh. 22 - Prob. 43PPCh. 22 - Prob. 44PPCh. 22 - Prob. 45PPCh. 22 - Prob. 46PPCh. 22 - Prob. 47PPCh. 22 - Prob. 48PPCh. 22 - Prob. 49PPCh. 22 - Prob. 50PPCh. 22 - Prob. 51PPCh. 22 - Prob. 52PPCh. 22 - Prob. 53PPCh. 22 - Prob. 54PPCh. 22 - Prob. 55PPCh. 22 - Prob. 56PPCh. 22 - Prob. 57PPCh. 22 - Prob. 58PPCh. 22 - Prob. 59PPCh. 22 - Prob. 60PPCh. 22 - Prob. 61PPCh. 22 - Prob. 62PPCh. 22 - Prob. 63PPCh. 22 - Prob. 64PPCh. 22 - Prob. 65PPCh. 22 - Prob. 66PPCh. 22 - Prob. 67PPCh. 22 - Prob. 68PPCh. 22 - Prob. 69PPCh. 22 - Prob. 70PPCh. 22 - Prob. 71PPCh. 22 - Prob. 72PPCh. 22 - Prob. 73IPCh. 22 - Prob. 74IPCh. 22 - Prob. 75IPCh. 22 - Prob. 76IPCh. 22 - Prob. 77IPCh. 22 - Prob. 78IPCh. 22 - Prob. 79IPCh. 22 - Prob. 80IPCh. 22 - Prob. 81IPCh. 22 - Prob. 82IPCh. 22 - Prob. 83IPCh. 22 - Prob. 84IPCh. 22 - Prob. 85IPCh. 22 - Prob. 86IPCh. 22 - Prob. 87IPCh. 22 - Prob. 88IPCh. 22 - Prob. 89IPCh. 22 - Prob. 90IPCh. 22 - Prob. 91IPCh. 22 - Prob. 92IPCh. 22 - Prob. 93IPCh. 22 - Prob. 94IPCh. 22 - Prob. 95IPCh. 22 - Prob. 96CPCh. 22 - Prob. 97CPCh. 22 - Prob. 98CPCh. 22 - Prob. 99CP
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY