BuyFindarrow_forward

Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079

Solutions

Chapter
Section
BuyFindarrow_forward

Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079
Textbook Problem

Draw the structure of the nitrogen-containing compound produced when each of the amides in Problem 17-140 is hydrolyzed with NaOH present (basic conditions).

Chapter 6, Problem 6.146EP, Draw the structure of the nitrogen-containing compound produced when each of the amides in Problem , example  1

Chapter 6, Problem 6.146EP, Draw the structure of the nitrogen-containing compound produced when each of the amides in Problem , example  2

Chapter 6, Problem 6.146EP, Draw the structure of the nitrogen-containing compound produced when each of the amides in Problem , example  3

Chapter 6, Problem 6.146EP, Draw the structure of the nitrogen-containing compound produced when each of the amides in Problem , example  4

(a)

Interpretation Introduction

Interpretation:

The structure of nitrogen-containing compound that is obtained when the given amide undergoes basic hydrolysis has to be drawn.

Concept Introduction:

Amides are derivatives of carboxylic acid.  Amides are not much reactive as of carboxylic acids.  They are also stable relatively in aqueous solution.  But under strenuous conditions amides undergo hydrolysis.  The conditions are presence of acid, base or enzymes.

Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt.  Amine salt is obtained because in acidic conditions the amine is converted into amine salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  1

Basic hydrolysis of amides gives the product as carboxylic acid salt and amine.  Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  2

Explanation

Basic hydrolysis of amides gives the product as carboxylic acid salt and amine.  Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.

Given compound structure is,

This amide on basic hydrolysis gives carboxylic acid salt and amine as the product...

(b)

Interpretation Introduction

Interpretation:

The structure of nitrogen-containing compound that is obtained when the given amide undergoes basic hydrolysis has to be drawn.

Concept Introduction:

Amides are derivatives of carboxylic acid.  Amides are not much reactive as of carboxylic acids.  They are also stable relatively in aqueous solution.  But under strenuous conditions amides undergo hydrolysis.  The conditions are presence of acid, base or enzymes.

Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt.  Amine salt is obtained because in acidic conditions the amine is converted into amine salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  3

Basic hydrolysis of amides gives the product as carboxylic acid salt and amine.  Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  4

(c)

Interpretation Introduction

Interpretation:

The structure of nitrogen-containing compound that is obtained when the given amide undergoes basic hydrolysis has to be drawn.

Concept Introduction:

Amides are derivatives of carboxylic acid.  Amides are not much reactive as of carboxylic acids.  They are also stable relatively in aqueous solution.  But under strenuous conditions amides undergo hydrolysis.  The conditions are presence of acid, base or enzymes.

Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt.  Amine salt is obtained because in acidic conditions the amine is converted into amine salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  5

Basic hydrolysis of amides gives the product as carboxylic acid salt and amine.  Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  6

(d)

Interpretation Introduction

Interpretation:

The structure of nitrogen-containing compound that is obtained when the given amide undergoes basic hydrolysis has to be drawn.

Concept Introduction:

Amides are derivatives of carboxylic acid.  Amides are not much reactive as of carboxylic acids.  They are also stable relatively in aqueous solution.  But under strenuous conditions amides undergo hydrolysis.  The conditions are presence of acid, base or enzymes.

Acidic hydrolysis of amides gives the product as carboxylic acid and amine salt.  Amine salt is obtained because in acidic conditions the amine is converted into amine salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  7

Basic hydrolysis of amides gives the product as carboxylic acid salt and amine.  Carboxylic acid salt is obtained because in basic conditions the carboxylic acid is converted into carboxylic acid salt.

Organic And Biological Chemistry, Chapter 6, Problem 6.146EP , additional homework tip  8

Still sussing out bartleby?

Check out a sample textbook solution.

See a sample solution

The Solution to Your Study Problems

Bartleby provides explanations to thousands of textbook problems written by our experts, many with advanced degrees!

Get Started
Sect-6.4 P-1QQSect-6.4 P-2QQSect-6.5 P-1QQSect-6.5 P-2QQSect-6.5 P-3QQSect-6.6 P-1QQSect-6.6 P-2QQSect-6.6 P-3QQSect-6.7 P-1QQSect-6.7 P-2QQSect-6.7 P-3QQSect-6.8 P-1QQSect-6.8 P-2QQSect-6.8 P-3QQSect-6.8 P-4QQSect-6.9 P-1QQSect-6.9 P-2QQSect-6.10 P-1QQSect-6.10 P-2QQSect-6.10 P-3QQSect-6.10 P-4QQSect-6.11 P-1QQSect-6.11 P-2QQSect-6.11 P-3QQSect-6.12 P-1QQSect-6.12 P-2QQSect-6.12 P-3QQSect-6.12 P-4QQSect-6.13 P-1QQSect-6.13 P-2QQSect-6.13 P-3QQSect-6.13 P-4QQSect-6.14 P-1QQSect-6.14 P-2QQSect-6.14 P-3QQSect-6.15 P-1QQSect-6.15 P-2QQSect-6.16 P-1QQSect-6.16 P-2QQSect-6.16 P-3QQSect-6.17 P-1QQSect-6.17 P-2QQSect-6.17 P-3QQSect-6.18 P-1QQSect-6.18 P-2QQSect-6.18 P-3QQSect-6.19 P-1QQSect-6.19 P-2QQSect-6.19 P-3QQSect-6.19 P-4QQCh-6 P-6.1EPCh-6 P-6.2EPCh-6 P-6.3EPCh-6 P-6.4EPCh-6 P-6.5EPCh-6 P-6.6EPCh-6 P-6.7EPCh-6 P-6.8EPCh-6 P-6.9EPCh-6 P-6.10EPCh-6 P-6.11EPCh-6 P-6.12EPCh-6 P-6.13EPCh-6 P-6.14EPCh-6 P-6.15EPCh-6 P-6.16EPCh-6 P-6.17EPCh-6 P-6.18EPCh-6 P-6.19EPCh-6 P-6.20EPCh-6 P-6.21EPCh-6 P-6.22EPCh-6 P-6.23EPCh-6 P-6.24EPCh-6 P-6.25EPCh-6 P-6.26EPCh-6 P-6.27EPCh-6 P-6.28EPCh-6 P-6.29EPCh-6 P-6.30EPCh-6 P-6.31EPCh-6 P-6.32EPCh-6 P-6.33EPCh-6 P-6.34EPCh-6 P-6.35EPCh-6 P-6.36EPCh-6 P-6.37EPCh-6 P-6.38EPCh-6 P-6.39EPCh-6 P-6.40EPCh-6 P-6.41EPCh-6 P-6.42EPCh-6 P-6.43EPCh-6 P-6.44EPCh-6 P-6.45EPCh-6 P-6.46EPCh-6 P-6.47EPCh-6 P-6.48EPCh-6 P-6.49EPCh-6 P-6.50EPCh-6 P-6.51EPCh-6 P-6.52EPCh-6 P-6.53EPCh-6 P-6.54EPCh-6 P-6.55EPCh-6 P-6.56EPCh-6 P-6.57EPCh-6 P-6.58EPCh-6 P-6.59EPCh-6 P-6.60EPCh-6 P-6.61EPCh-6 P-6.62EPCh-6 P-6.63EPCh-6 P-6.64EPCh-6 P-6.65EPCh-6 P-6.66EPCh-6 P-6.67EPCh-6 P-6.68EPCh-6 P-6.69EPCh-6 P-6.70EPCh-6 P-6.71EPCh-6 P-6.72EPCh-6 P-6.73EPCh-6 P-6.74EPCh-6 P-6.75EPCh-6 P-6.76EPCh-6 P-6.77EPCh-6 P-6.78EPCh-6 P-6.79EPCh-6 P-6.80EPCh-6 P-6.81EPCh-6 P-6.82EPCh-6 P-6.83EPCh-6 P-6.84EPCh-6 P-6.85EPCh-6 P-6.86EPCh-6 P-6.87EPCh-6 P-6.88EPCh-6 P-6.89EPCh-6 P-6.90EPCh-6 P-6.91EPCh-6 P-6.92EPCh-6 P-6.93EPCh-6 P-6.94EPCh-6 P-6.95EPCh-6 P-6.96EPCh-6 P-6.97EPCh-6 P-6.98EPCh-6 P-6.99EPCh-6 P-6.100EPCh-6 P-6.101EPCh-6 P-6.102EPCh-6 P-6.103EPCh-6 P-6.104EPCh-6 P-6.105EPCh-6 P-6.106EPCh-6 P-6.107EPCh-6 P-6.108EPCh-6 P-6.109EPCh-6 P-6.110EPCh-6 P-6.111EPCh-6 P-6.112EPCh-6 P-6.113EPCh-6 P-6.114EPCh-6 P-6.115EPCh-6 P-6.116EPCh-6 P-6.117EPCh-6 P-6.118EPCh-6 P-6.119EPCh-6 P-6.120EPCh-6 P-6.121EPCh-6 P-6.122EPCh-6 P-6.123EPCh-6 P-6.124EPCh-6 P-6.125EPCh-6 P-6.126EPCh-6 P-6.127EPCh-6 P-6.128EPCh-6 P-6.129EPCh-6 P-6.130EPCh-6 P-6.131EPCh-6 P-6.132EPCh-6 P-6.133EPCh-6 P-6.134EPCh-6 P-6.135EPCh-6 P-6.136EPCh-6 P-6.137EPCh-6 P-6.138EPCh-6 P-6.139EPCh-6 P-6.140EPCh-6 P-6.141EPCh-6 P-6.142EPCh-6 P-6.143EPCh-6 P-6.144EPCh-6 P-6.145EPCh-6 P-6.146EPCh-6 P-6.147EPCh-6 P-6.148EPCh-6 P-6.149EPCh-6 P-6.150EPCh-6 P-6.151EPCh-6 P-6.152EPCh-6 P-6.153EPCh-6 P-6.154EP

Additional Science Solutions

Find more solutions based on key concepts

Show solutions add

Why do you think a dye is added to antifreeze before it is sold in stores?

Chemistry for Today: General, Organic, and Biochemistry

4. The normal arterial range is

Cardiopulmonary Anatomy & Physiology

Why do biologists often use model organisms in their research?

Biology: The Dynamic Science (MindTap Course List)

In the following diagram, designate each daughter cell as diploid (2n) or haploid (n).

Human Heredity: Principles and Issues (MindTap Course List)

A daily regimen of supplements and vitamin D-enriched foods increases the risk of vitamin D toxicity. T F

Nutrition: Concepts and Controversies - Standalone book (MindTap Course List)

A child is practicing for a BMX race. His speed remains constant as he goes counterclockwise around a level tra...

Physics for Scientists and Engineers, Technology Update (No access codes included)