(a) Interpretation: For the given molecule, the IUPAC is to be written. Concept introduction: The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

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Answer 1

Question

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

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Students have asked these similar questions

Draw the structure of the product that will be formed when each of the following amines reacts with sodium nitrite and hydrochloric acid, followed by cuprous chloride. (a) propylamine

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Which of the following compounds contains an amide?

Answer 2

Question

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

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Answer 3

Question

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

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Answer 4

Question

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

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Answer 5

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 6

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 7

Chapter F, Problem F.18P

Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 8

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 9

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 10

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 11

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. F - Prob. F.1P Ch. F - Prob. F.2P Ch. F - Prob. F.3P Ch. F - Prob. F.4P Ch. F - Prob. F.5P Ch. F - Prob. F.6P Ch. F - Prob. F.7P Ch. F - Prob. F.8P Ch. F - Prob. F.9P Ch. F - Prob. F.10P

Solution Summary: The author explains that the IUPAC name of an amide is made of two parts: the first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid

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