The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained. Concept Introduction: Haworth projection: The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection . Conformational isomers: The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers. The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position. The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position . The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Question

Want to see the full answer?

Answer 1

Question

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

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 and correct answer

Predict the product formed when the compound shown below undergoes a reaction with MCPBA in CH2Cl2. MCPBA is meta-chloroperoxybenzoic acid.

Answer 2

Question

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Answer 6

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

Answer 7

Chapter 4.14, Problem 34CC

Interpretation Introduction

Interpretation:

The Haworth projections of cis and trans-1-4-dimethylcyclohexane are drawn and its stability should be comparatively explained.

Concept Introduction:

Haworth projection:

The representation of cyclic chemical compounds by normal ring structure and the substituents can either pointing up or down on this ring is called Haworth projection.

Conformational isomers:

The two or more compounds have same molecular formula and different structural formulas from the result of C-C single bond rotations are called conformational isomers.

The atom or group is occupy at similar to a vertical axis passing through the chair conformation of Cyclohexane ring is called axial position.

The atom or group is occupy at similar to horizontal axis passing through the chair conformation of ring is called equatorial position.

The substituents are occupy in equatorial position is more stable than axial because of the 1,3-diaxial interactions are less in equatorial position.

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. 4.2 - Prob. 1LTS Ch. 4.2 - Prob. 1PTS Ch. 4.2 - Prob. 2PTS Ch. 4.2 - Prob. 3ATS Ch. 4.2 - Prob. 2LTS Ch. 4.2 - Prob. 4PTS Ch. 4.2 - Prob. 5ATS Ch. 4.2 - Prob. 3LTS Ch. 4.2 - Prob. 6PTS Ch. 4.2 - Prob. 7ATS

Want to see the full answer?

Chapter 4 Solutions