ORGANIC CHEMISTRY BOOK& SG/SM
ORGANIC CHEMISTRY BOOK& SG/SM
6th Edition
ISBN: 9781264094493
Author: SMITH
Publisher: MCG
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Chapter 26, Problem 64P
Interpretation Introduction

Interpretation: The D-aldopentose which on oxidation produces optically active aldaric acid and that undergoes Wohl Degradation to yield D-aldotetrose which on oxidation produces optically active aldaric acid is to be predicted.

Concept introduction: Carbohydrates containing aldehydes are known as aldoses. Wohl Degradation is a method of shortening the aldose by one carbon atom by cleavage of C1C2 bond.

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Which D-aldopentose is oxidized to an optically active aldaric acid and undergoes the Wohl degradation to yield a D-aldotetrose that is oxidized to an optically active aldaric acid?
D-Aldopentose A is oxidized to an optically inactive aldaric acid. On Wohl degradation, A forms an aldotetrose B that is oxidized to an optically active aldaric acid. What are the structures of A and B?
Identify compounds A–D. A D-aldopentose A is oxidized with HNO3 to an optically inactive aldaric acid B. A undergoes the Kiliani–Fischer synthesis to yield C and D. C is oxidized to an optically active aldaric acid. D is oxidized to an optically inactive aldaric acid

Chapter 26 Solutions

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