The most stable isomer among the cis and trans isomers of the given compound is to be determined. Concept introduction: When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Question

Want to see the full answer?

Answer 1

Question

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

6. For each of the following, determine whether the cis or trans isomer is more stable. You actually did this in the above question. LEt Et Et more stable? cis or trans? number of axial H-atoms: number of equatorial H-atoms:

Both cis and trans isomers exist for this molecule. Which one is more stable?

Consider 1,2-dimethylcyclohexane.Q: Which isomer, cis or trans, is more stable and why?

Answer 2

Question

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Answer 6

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Answer 7

Chapter 4, Problem 4.45P

Interpretation Introduction

Interpretation:

The most stable isomer among the cis and trans isomers of the given compound is to be determined.

Concept introduction:

When the bulkier substituent attached to a cyclohexane ring is in the equatorial position, the chair conformation is more favored. In the disubstituted cyclohexane, the substituents which are on the opposite side of the ring are trans to each other. If there are more than one substituent attached, then the conformation in which maximum substituents are in the equatorial position is favored and is more stable.

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

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 isomer of a given compound is the trans one, which has all equatorial bonds and no crowding of hydrogen atoms.

Concept explainers

Want to see the full answer?

Chapter 4 Solutions