(a) Interpretation: The IUPAC name of the ter-butyl ethyl ether is to be written. Concept introduction: The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

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Answer 1

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Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

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Provide the IUPAC name of the molecule shown below. NH

Indicate whether each statement is true or false. (a) Alkanesdo not contain any carbon–carbon multiple bonds.(b) Cyclobutane contains a four-membered ring. (c) Alkenescontain carbon–carbon triple bonds. (d) Alkynes containcarbon–carbon double bonds. (e) Pentane is a saturatedhydrocarbon but 1-pentene is an unsaturated hydrocarbon.(f) Cyclohexane is an aromatic hydrocarbon. (g) The methylgroup contains one less hydrogen atom than methane.

Draw the structure for the following compound. (R)-3-methylhexane

Answer 2

Question

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

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Answer 3

Question

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

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Answer 4

Question

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

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Answer 5

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 6

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 7

Chapter A, Problem A.17P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the ter-butyl ethyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The IUPAC name of the cyclohexyl methyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The IUPAC name of sec-butyl propyl ether is to be written.

Concept introduction:

The IUPAC name of an ether is written in the form of alkoxyalkane. Out of the two alkyl groups attached to the oxygen atom, the longest carbon chain is considered as the root. The other alkyl group is written as an alkoxy substituent. The name of the alkoxy substituent is obtained by replacing the suffix –yl from the name of the alkyl group by the suffix –oxy.

Answer 12

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Answer 13

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Answer 14

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Answer 15

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

Solution Summary: The author explains that the IUPAC name of ter-butyl ether is written in the form of alkoxyalkane.

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