(a) Interpretation: The three distinct chair conformations for cyclohexylcyclohexane is to be drawn. Concept introduction: Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

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Answer 1

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Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

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Answer 2

Question

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

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Answer 3

Question

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

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Answer 4

Question

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

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Answer 5

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

Answer 6

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Answer 7

Chapter 4, Problem 4.38P

Interpretation Introduction

(a)

Interpretation:

The three distinct chair conformations for cyclohexylcyclohexane is to be drawn.

Concept introduction:

Chair conformations have three sets of parallel lines drawn together at a time. Equatorial bonds are drawn parallel to the line representing the C-C bonds in the ring while axial bonds are drawn up or down to the ring. On the chair conformations, axial bonds alternate up and down around the ring, whereas, equatorial bonds alternate slightly up and down around the ring. The structure of cyclohexane in the chair form is shown as:

Answer 8

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The most stable conformation of cyclohexylcyclohexane is to be determined.

Concept introduction:

When each substituent is attached to a cyclohexane ring in an equatorial position, the chair conformation is most stable than in an axial position. In the monosubstituted cyclohexane, the substituents that are attached to equatorial positions of each other are most stable. If two or more substituents are attached to cyclohexane, then the conformation in which maximum substituents are in equatorial position is more stable than the axial position.

Answer 10

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Answer 12

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Answer 13

Ch. 4 - Prob. 4.1P Ch. 4 - Prob. 4.2P Ch. 4 - Prob. 4.3P Ch. 4 - Prob. 4.4P Ch. 4 - Prob. 4.5P Ch. 4 - Prob. 4.6P Ch. 4 - Prob. 4.7P Ch. 4 - Prob. 4.8P Ch. 4 - Prob. 4.9P Ch. 4 - Prob. 4.10P

Solution Summary: The author explains how the three distinct chair conformations of cyclohexylcyclexane are to be drawn.

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