a) Interpretation: The name of the cycloalkane shown is to be given. Concept introduction: The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C 1 & C 2 and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C 1 & C 2 . In dienes and trienes, however the position of double bonds is shown. To name: The cycloalkane shown.

Question

Which of the following compounds is (S)-4-chloro-1-methylcyclohexene? CH3 CH3 CH3 CH3 A C D

Answer 1

Question

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

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Answer 2

Question

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

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Answer 3

Question

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

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Answer 4

Question

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

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Answer 5

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 6

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 7

Chapter 7.SE, Problem 39AP

Interpretation Introduction

a)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 8

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 9

Interpretation Introduction

b)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 10

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 11

Interpretation Introduction

c)

Interpretation:

The name of the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 12

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 13

Interpretation Introduction

d)

Interpretation:

The name the cycloalkane shown to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 14

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Answer 15

Interpretation Introduction

e)

Interpretation:

The name the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkaneâ€“the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown

Answer 16

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 17

Interpretation Introduction

f)

Interpretation:

The name of the cycloalkane shown is to be given.

Concept introduction:

The maximum number of carbons in the ring is counted. Based on the name of the parent cycloalkane–the cycloalkene is named with the suffix–ene. The cycloalkane is numbered such that the double bond is in between C₁ & C₂ and the first substituent has the lowest number possible. Usually the position of a double bond is not shown in the name because it is always between C₁ & C₂. In dienes and trienes, however the position of double bonds is shown.

To name:

The cycloalkane shown.

Answer 18

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Answer 19

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Answer 29

Ch. 7.2 - Calculate the degree of unsaturation in each of...Ch. 7.2 - Prob. 2P Ch. 7.2 - Diazepam, marketed as an antianxiety medication...Ch. 7.3 - Give IUPAC names for the following compounds:Ch. 7.3 - Prob. 5P Ch. 7.3 - Prob. 6P Ch. 7.3 - Prob. 7P Ch. 7.4 - Prob. 8P Ch. 7.4 - Prob. 9P Ch. 7.4 - Prob. 10P

Solution Summary: The author explains that the IUPAC name of the compound is 3-methylcyclohexene.

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Chapter 7 Solutions