Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 7, Problem 7.9P
Interpretation Introduction

(a)

Interpretation:

The planar-ring structure that results from the given rotation of the structure is to be drawn.

Concept introduction:

The conformation of cyclohexane is a type of 3D shape of cyclohexane molecule. There are total four types of significant conformations of cyclohexane exists which are chair conformation, half-chair conformation, boat conformation and twist-boat conformation. In trans- configuration the two groups remains at the opposite side to each other.

Interpretation Introduction

(b)

Interpretation:

The planar-ring structure that results from the given rotation of the structure is to be drawn.

Concept introduction:

The conformation of cyclohexane is a type of 3D shape of cyclohexane molecule. There are total four types of significant conformations of cyclohexane exists which are chair conformation, half-chair conformation, boat conformation and twist-boat conformation. In trans- configuration the two groups remains at the opposite side to each other.

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Although we learned in Section 5.4 that uncharged nitrogen atoms generally cannot be chiral centers (due to nitrogen inversion), an exception is Tröger's base. Tröger's base has two enantiomers that can be separated from each other. They are different in their configurations at the N atoms. One enantiomer is shown on the right, viewed from two different perspectives. (a) Draw the second enantiomer of Tröger's base. (b) Explain why the two enantiomers do not interconvert. Tröger's base
6. Draw in the curved arrows to convert the left structure to the right structure (3 points) (a) (b) (+ H₂C OCH3 CH3 H₂C 0 OCH3 CH3
(A) Indicate the positions (axial or equatorial) of the two substituents (a, b) in the most stable chair conformation. (B) Indicate the positions (axial or equatorial) of the two substituents (a, b) of Enantiomer in the most stable chair conformation. b

Chapter 7 Solutions

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