ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
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Chapter 7, Problem 7.56AP
Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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2. Name the following hydrocarbons. (9 marks) a) HHHHHHHH H-C-C- H-O-S b) HCEC-CH3 H H H H H d) c) H C=C- H H H e) CH3 CH3 CH2CH=CH-CH=CHCH3 HHHH H-C-C-C-C-H H HH H f) large CH2CH3 pola H3C section lovels tower, able ocart firs g) Tower H3C-CH2 then in H3C-CH-CH-CH3 enblbano bne noitsidab Copyright © 2008. Durham Continuing Education CH3

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