ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259977596
Author: SMITH
Publisher: MCG
Question
Book Icon
Chapter 25, Problem 25.29P
Interpretation Introduction

(a)

Interpretation: The product formed by the treatment of given compound with NaNO2 and HCl is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

Expert Solution
Check Mark

Answer to Problem 25.29P

The product formed by the treatment of given compound with NaNO2 and HCl is shown below.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  1

Explanation of Solution

Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

In the given compound, nitrogen atom is substituted by two hydrogen atoms and one phenyl group. Hence, it is a primary amine. Therefore, the product formed by the reaction of given compound with NaNO2 and HCl is aryl diazonium salt as shown in Figure 1.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  2

Figure 1

Conclusion

The product formed by the treatment of given compound with NaNO2 and HCl is shown in Figure 1.

Interpretation Introduction

(b)

Interpretation: The product formed by the treatment of given compound with NaNO2 and HCl is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

Expert Solution
Check Mark

Answer to Problem 25.29P

The product formed by the treatment of given compound with NaNO2 and HCl is shown below.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  3

Explanation of Solution

Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

In the given compound, nitrogen atom is substituted by one hydrogen atom and two alkyl groups. Hence, it is a secondary amine. Therefore, the product formed by the reaction of given compound with NaNO2 and HCl is N-nitrosamine as shown in Figure 2.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  4

Figure 2

Conclusion

The product formed by the treatment of given compound with NaNO2 and HCl is shown in Figure 2.

Interpretation Introduction

(c)

Interpretation: The product formed by the treatment of given compound with NaNO2 and HCl is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

Expert Solution
Check Mark

Answer to Problem 25.29P

The product formed by the treatment of given compound with NaNO2 and HCl is shown below.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  5

Explanation of Solution

Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

In the given compound, nitrogen atom is substituted by one hydrogen atom and two alkyl groups. Hence, it is a secondary amine. Therefore, the product formed by the reaction of given compound with NaNO2 and HCl is N-nitrosamine as shown in Figure 3.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  6

Figure 3

Conclusion

The product formed by the treatment of given compound with NaNO2 and HCl is shown in Figure 3.

Interpretation Introduction

(d)

Interpretation: The product formed by the treatment of given compound with NaNO2 and HCl is to be drawn.

Concept introduction: Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

Expert Solution
Check Mark

Answer to Problem 25.29P

The product formed by the treatment of given compound with NaNO2 and HCl is shown below.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  7

Explanation of Solution

Primary and secondary amines on reaction with NaNO2 in the presence of HCl yield different products. Diazonium salt is formed by the reaction of primary amine with NaNO2+HCl whereas N-nitrosamine is formed by the reaction of secondary amine with NaNO2+HCl.

In the given compound, nitrogen atom is substituted by two hydrogen atoms and one alkyl group. Hence, it is a primary amine. Therefore, the product formed by the reaction of given compound with NaNO2 and HCl is alkyl diazonium salt as shown in Figure 4.

ORGANIC CHEMISTRY, Chapter 25, Problem 25.29P , additional homework tip  8

Figure 4

Conclusion

The product formed by the treatment of given compound with NaNO2 and HCl is shown in Figure 4.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Draw the products formed when each compound is treated with HNO3 and H2SO4.
Draw the products formed when each ether is treated with two equivalents of HBr.
Compound that is most easily hydrolyzed by acid in water `NH A. В. F C. D.

Chapter 25 Solutions

ORGANIC CHEMISTRY

Ch. 25 - Prob. 25.11PCh. 25 - Prob. 25.12PCh. 25 - Prob. 25.13PCh. 25 - Prob. 25.14PCh. 25 - Prob. 25.15PCh. 25 - Prob. 25.16PCh. 25 - Prob. 25.17PCh. 25 - Problem 25.18 Write out steps to show how each of...Ch. 25 - Prob. 25.19PCh. 25 - Prob. 25.20PCh. 25 - Prob. 25.21PCh. 25 - Problem 25.22 Which nitrogen atom in each compound...Ch. 25 - Prob. 25.23PCh. 25 - Prob. 25.24PCh. 25 - Prob. 25.25PCh. 25 - Prob. 25.26PCh. 25 - Prob. 25.27PCh. 25 - Problem 25.28 Draw the major product formed in...Ch. 25 - Prob. 25.29PCh. 25 - Prob. 25.30PCh. 25 - Problem 25.31 Devise a synthesis of each compound...Ch. 25 - Prob. 25.32PCh. 25 - Problem 25.33 What starting materials are needed...Ch. 25 - Problem 25.34 (a) What two components are needed...Ch. 25 - Prob. 25.35PCh. 25 - Prob. 25.36PCh. 25 - 25.37 Varenicline (trade name Chantix) is a drug...Ch. 25 - Give a systematic or common name for each...Ch. 25 - Prob. 25.39PCh. 25 - 25.40 How many stereogenic centers are present in...Ch. 25 - 25.41 Rank the compounds in each group in order of...Ch. 25 - 25.42 Decide which atom in each molecule is most...Ch. 25 - 25.43 Explain why pyrimidine is less basic than...Ch. 25 - 25.44 Rank the nitrogen atoms in each compound in...Ch. 25 - 25.45 Explain why nitroaniline is a stronger base...Ch. 25 - 25.46 Explain the observed difference in the...Ch. 25 - 25.47 Why is pyrrole more acidic than...Ch. 25 - Prob. 25.48PCh. 25 - Prob. 25.49PCh. 25 - Prob. 25.50PCh. 25 - 25.51 How would you separate toluene , benzoic...Ch. 25 - 25.52 Draw the products formed when methylaniline ...Ch. 25 - Prob. 25.53PCh. 25 - Prob. 25.54PCh. 25 - 25.55 Draw the organic products formed in each...Ch. 25 - Prob. 25.56PCh. 25 - 25.57 Identify A, B, and C, three intermediates in...Ch. 25 - Prob. 25.58PCh. 25 - Prob. 25.59PCh. 25 - 25.60 A chiral amine A having the configuration...Ch. 25 - 25.61 Draw a stepwise mechanism for each...Ch. 25 - 25.62 Draw a stepwise mechanism for the following...Ch. 25 - Prob. 25.63PCh. 25 - 25.64 Tertiary aromatic amines react with and ...Ch. 25 - 25.65 Devise a synthesis of each compound from...Ch. 25 - Prob. 25.66PCh. 25 - Prob. 25.67PCh. 25 - Prob. 25.68PCh. 25 - Prob. 25.69PCh. 25 - 25.70 Devise a synthesis of each biologically...Ch. 25 - 25.71 Devise a synthesis of each compound from...Ch. 25 - 25.72 Three isomeric compounds A, B, and C, all...Ch. 25 - 25.73 Treatment of compound D with LiAlH4 followed...Ch. 25 - Prob. 25.74PCh. 25 - 25.75 Rank the following compounds in order of...Ch. 25 - Prob. 25.76PCh. 25 - Prob. 25.77PCh. 25 - Prob. 25.78P
Knowledge Booster
Background pattern image
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