The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn. Concept introduction: Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

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Answer 1

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Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

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Answer 2

Question

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

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Answer 3

Question

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

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Answer 4

Question

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

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Answer 5

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

Answer 6

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

Answer 7

Chapter 4, Problem 4.14P

Interpretation Introduction

Interpretation:

The most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

Concept introduction:

Each substituent attached to a cyclohexane ring in an equatorial position, the chair conformation, is most stable than in an axial position. In the disubstituted cyclohexane, the substituents which are on the same side of the ring are cis to each other. Substituents that are cis to each other in one chair conformation remain cis after the chair flip. If there are more than one substituent attached to cyclohexane, the conformation in which maximum substituents are in the equatorial position is more stable than the axial position.

Answer 8

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Answer 11

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 that the most stable conformation of cis-1-methyl-4-trichloromethylcyclohexane is to be drawn.

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