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.

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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.

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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.

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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.

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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.

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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

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Answer 9

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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

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