(a) Interpretation: The chair form of trans -and cis -decalin for the cyclohexane rings are to be drawn. Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds. The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position. The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Question

Want to see the full answer?

Answer 1

Question

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Don't used hand raiting and don't used Ai solution

Determine the number of protons (p), neutrons (n), or electrons (e) in each of thefollowing:

using dimensional analysis convert 15.28 lb/gallon to mg/mL

Answer 2

Question

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Answer 6

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Answer 7

Chapter 4, Problem 74P

Interpretation Introduction

(a)

Interpretation: The chair form of trans-and cis-decalin for the cyclohexane rings are to be drawn.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. The chair conformation of cyclohexane consists of six axial and six equatorial bonds.

The six axial bonds present one on each carbon atom, are parallel and alternate to each other and are in up-down position.

The six equatorial bonds present one on each carbon atom, are present in three sets of two parallel ring bonds. They are in alternate position between the sides around the ring.

Answer 8

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Answer 9

Interpretation Introduction

(b)

Interpretation: An explanation corresponding to the fact that the trans isomer is more stable is to be stated.

Concept introduction: The different spatial arrangements of atoms that results from the rotation about single bonds are called conformational isomers. When two substituents in a conformation are in up or down direction then it is known as cis conformation. But if one substituent is in upward direction and the other is facing down direction, then the conformation is known as trans.

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 13

Ch. 4.1 - Prob. 1P Ch. 4.1 - Problem 4.2 Which of the following is not another...Ch. 4.1 - Problem 4.3 Draw the five constitutional isomers...Ch. 4.1 - Prob. 4P Ch. 4.1 - Prob. 5P Ch. 4.2 - Draw the five constitutional isomers that have...Ch. 4.4 - Problem 4.7 Give the IUPAC name for each...Ch. 4.4 - Give the IUPAC name for each compound. a....Ch. 4.4 - Problem 4.9 Give the structure corresponding to...Ch. 4.4 - Prob. 10P

Solution Summary: The author explains the different spatial arrangements of atoms that result from the rotation about single bonds are called conformational isomers.

Concept explainers

Want to see the full answer?

Chapter 4 Solutions