Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 24, Problem 24.47AP
Interpretation Introduction

Interpretation:

The structure of compound A which is a monomethyl ether of D-glucose is to be stated.

Concept introduction:

Ruff degradation is a process in which an aldose is converted into another aldose containing one carbon less than the starting aldose. In this process, an aldose is converted into aldonic acid by oxidation with Br2/H2O and Ca(OH)2. The decarboxylation of calcium salt of aldonic acid occurs when it is treated with Fe and H2O2 and results in the formation of an aldose containg a carbon atom less than the starting aldose.

Killani Fischer synthesis is the three step process: conversion of aldose into cyanohydrins; hydrolysis; and reduction. The overall use of Killani Fischer synthesis is to synthesize two diastereomeric aldoses with an increased asymmetric carbon from an aldose.

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A D-aldopentose A is oxidized to an optically inactive aldaric acid with HNO3. A is formed by the Kiliani–Fischer synthesis of a D-aldotetrose B, which is also oxidized to an optically inactive aldaric acid with HNO3. What are the structures of A and B?
An aldose A, is reduced by sodium borohydride to an optically inactive alditol B. The Ruff degredation of A forms C. Oxidation of C by nitric acid generates the optically inactive diacid D. The ruff degreation of C forms D-glyceraldehyde. draw the structures for compounds A through D and discuss a mechanism for the reduction step using sodium borohydride
(a) Which of the d-aldopentoses will give optically active aldaric acids on oxidation with HNO3 ?(b) Which of the d-aldotetroses will give optically active aldaric acids on oxidation with HNO3 ?(c) Sugar X is known to be a d-aldohexose. On oxidation with HNO3, X gives an optically inactive aldaric acid. WhenX is degraded to an aldopentose, oxidation of the aldopentose gives an optically active aldaric acid. Determine thestructure of X.(d) Even though sugar X gives an optically inactive aldaric acid, the pentose formed by degradation gives an opticallyactive aldaric acid. Does this finding contradict the principle that optically inactive reagents cannot form opticallyactive products?(e) Show what product results if the aldopentose formed from degradation of X is further degraded to an aldotetrose.Does HNO3 oxidize this aldotetrose to an optically active aldaric acid?
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