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Organic And Biological Chemistry

7th Edition
STOKER + 1 other
ISBN: 9781305081079

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Chapter
Section
BuyFindarrow_forward

Organic And Biological Chemistry

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

Assign an IUPAC name to each of the following amides.

Chapter 6, Problem 6.112EP, Assign an IUPAC name to each of the following amides. , example  1

Chapter 6, Problem 6.112EP, Assign an IUPAC name to each of the following amides. , example  2

Chapter 6, Problem 6.112EP, Assign an IUPAC name to each of the following amides. , example  3

Chapter 6, Problem 6.112EP, Assign an IUPAC name to each of the following amides. , example  4

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid.  This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

  • The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
  • The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Explanation

Given structure of compound is,

The IUPAC name of parent carboxylic acid is found to be butanoic acid...

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid.  This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

  • The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
  • The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid.  This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

  • The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
  • The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid.  This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

  • The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.
  • The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

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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

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