(a) Interpretation: The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected. Concept introduction: when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa. When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

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Answer 1

Question

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

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Answer 2

Question

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

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Answer 3

Question

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

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Answer 4

Question

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

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Answer 5

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

Answer 6

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Answer 7

Chapter 26, Problem 47E

Interpretation Introduction

(a)

Interpretation:

The two possible chair conformations for the cyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexanering converts from one chair conformation to another, the equatorial hydrogen atoms areconverted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial and most stable conformer should be selected.

Concept introduction:

when the cyclohexane ring converts from one chair conformation to another, the equatorial hydrogen atoms are converted into axial hydrogen atoms and vice versa.

When the cyclohexane has one substituent then the conformation which contain the substituent in equatorial position is more stable due to less steric strain with axial hydrogen atoms.

When two substituents are present in the structure, in order to find the more stable conformation can be determined by looking at the groups in the axial position.

When a bulkier group present in the axial position, that conformation get less stable.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 26 - Prob. 1E Ch. 26 - Draw a structural formula for each of the...Ch. 26 - Prob. 3E Ch. 26 - Write structural formulas corresponding to these...Ch. 26 - Prob. 5E Ch. 26 - Prob. 6E Ch. 26 - Prob. 7E Ch. 26 - Prob. 8E Ch. 26 - What is the relationship, if any, between the...Ch. 26 - Prob. 10E

Solution Summary: The author explains that the two possible chair conformations for the trans-3-methylcyclohexanol should be drawn and named every substituent as axial or equatorial.

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