Study Guide with Student Solutions Manual for McMurry's Organic Chemistry, 9th
Study Guide with Student Solutions Manual for McMurry's Organic Chemistry, 9th
9th Edition
ISBN: 9781305082144
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 25.SE, Problem 44AP
Interpretation Introduction

Interpretation:

From the cyclic structure of allose given, whether it is i) a furanose or pyranose form ii) α- or β- anomer iii) D or L sugar are to be stated.

Concept introduction:

The pyranose form is a cyclic hemiacetal form with a six membered ring formed by the nucleophilic addition of the –OH group on C5 to the C1 carbonyl group. The furanose form is a cyclic hemiacetal form with a five membered ring formed by the nucleophilic addition of the –OH group on C5 to the C2 carbonyl group.

The orientation of –OH group differs in α- and β- anomers. In α- anomer the OH on C1 is cis to the –OH at the lowest chirality center in Fischer projection, while in β- anomer the –OH on C1 is trans to the –OH at the lowest chirality center in Fischer projection.

D sugars have the –O- at C5 on the right in the uncoiled form while L sugars have -O- at C5 on the left.

To state:

From the cyclic structure of allose given, whether it is i) a furanose or pyranose form ii) α- or β- anomer iii) D or L sugar.

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Study Guide with Student Solutions Manual for McMurry's Organic Chemistry, 9th

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