The most stable pyranose conformation of the given carbohydrate is to be identified. Concept introduction: In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form. The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form. The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Question

Want to see the full answer?

Answer 1

Question

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

The number of noncyclic isomers that have the composition C4H8Owith the O as part of an OH group, counting a pair of stereoisomers as1, is A. 8; B. 6; C. 9; D. 5; E. None of the other answers is correct.

None

The number of carbon skeletons that have 8 carbons, one of which istertiary is A. 7; B. More than 7; C. 6; D. 5; E. 4

Answer 2

Question

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Answer 6

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Answer 7

Chapter 3, Problem 52DSP

Interpretation Introduction

Interpretation:

The most stable pyranose conformation of the given carbohydrate is to be identified.

Concept introduction:

In the structure of planar cyclohexane, the substituents that are on the wedge bonds must be above the plane of the ring in the chair form.

The substituents that are on the dash bond in the planar cyclohexane must be below the plane of the ring in the chair form.

The most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

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. 3.1 - Identify the alkanes corresponding to each of the...Ch. 3.1 - Find the conformations in Figure 3.4 in which the...Ch. 3.2 - Sketch a potential energy diagram for rotation...Ch. 3.2 - Acetylcholine is a neurotransmitter in the central...Ch. 3.2 - Prob. 5P Ch. 3.5 - The heats of combustion of ethylcyclopropane and...Ch. 3.8 - Prob. 7P Ch. 3.10 - The following questions relate to a cyclohexane...Ch. 3.10 - Draw the most stable conformation of...Ch. 3.11 - Prob. 10P

Solution Summary: The author explains that the most stable conformation of a cycloalkane is the one in which most of the substituents occupy equatorial orientation.

Concept explainers

Want to see the full answer?

Chapter 3 Solutions