Organic Chemistry: Structure and Function
Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Chapter 5, Problem 36P

(a)

Interpretation Introduction

Interpretation: Whether the indicated cyclohexane derivative is chiral or not should be identified.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 36P , additional homework tip  1

Concept introduction: Four kinds of symmetry elements that may be present are tabulated as follows:

  S.NoSymmetry elementNotation1.Axis of symmetryCn2.Plane of symmetryσ3. Alternating axis of  symmetrySn4.Center of symmetryi

The enantiomers are identical chemical compounds that have a mirror-image relationship to each other while diastereomers do not hold mirror image relationships. The former are chiral and optically active while the latter can be chiral or achiral.

Any organic compound must have no plane of symmetry in order to be optically active. The compounds with any plane of symmetry are achiral and optically inactive.

(b)

Interpretation Introduction

Interpretation: Whether the indicated cyclohexane derivative is chiral or not should be identified.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 36P , additional homework tip  2

Concept introduction: Four kinds of symmetry elements that may be present are tabulated as follows:

  S.NoSymmetry elementNotation1.Axis of symmetryCn2.Plane of symmetryσ3. Alternating axis of  symmetrySn4.Center of symmetryi

The enantiomers are identical chemical compounds that have a mirror-image relationship to each other while diastereomers do not hold mirror image relationships. The former are chiral and optically active while the latter can be chiral or achiral.

Any organic compound must have no plane of symmetry in order to be optically active. The compounds with any plane of symmetry are achiral and optically inactive.

(c)

Interpretation Introduction

Interpretation: Whether the indicated cyclohexane derivative is chiral or not should be identified.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 36P , additional homework tip  3

Concept introduction: Four kinds of symmetry elements that may be present are tabulated as follows:

  S.NoSymmetry elementNotation1.Axis of symmetryCn2.Plane of symmetryσ3. Alternating axis of  symmetrySn4.Center of symmetryi

The enantiomers are identical chemical compounds that have a mirror-image relationship to each other while diastereomers do not hold mirror image relationships. The former are chiral and optically active while the latter can be chiral or achiral.

Any organic compound must have no plane of symmetry in order to be optically active. The compounds with any plane of symmetry are achiral and optically inactive.

(d)

Interpretation Introduction

Interpretation: Whether the indicated cyclohexane derivative is chiral or not should be identified.

  Organic Chemistry: Structure and Function, Chapter 5, Problem 36P , additional homework tip  4

Concept introduction: Four kinds of symmetry elements that may be present are tabulated as follows:

  S.NoSymmetry elementNotation1.Axis of symmetryCn2.Plane of symmetryσ3. Alternating axis of  symmetrySn4.Center of symmetryi

The enantiomers are identical chemical compounds that have a mirror-image relationship to each other while diastereomers do not hold mirror image relationships. The former are chiral and optically active while the latter can be chiral or achiral.

Any organic compound must have no plane of symmetry in order to be optically active. The compounds with any plane of symmetry are achiral and optically inactive.

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Students have asked these similar questions
assign the stereochemical configuration of the selected tetrahedral carbon chiral centers (R, S or N (not a chiral center)) and the alkene (E, Z or N (not a stereocenter)) that are indicated by the arrows (note that you do not have to assign the configuration of every chiral center in the molecule). If the atom in question is not a chiral center or is not a stereocenter circle N for neither.
Is there a difference in the stability of the two cyclohexane conformations?
calculate the amount of steric strain in each of the chair conformers of 1,1,3-trimethylcyclohexane. Which conformer predominates at equilibrium?
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