Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 20, Problem 37P
Interpretation Introduction

Interpretation:

The structures of D-xylose and D-lyxose are to be drawn.

Concept Introduction:

Carbohydrates are naturally occurring organic compounds.  As the name implies carbohydrates are hydrates of carbon and have general formula of CX(H2O)Y.  Basically, carbohydrates are polyhydroxy aldehyde and ketones, for examples, glucose and fructose.

Sugars are classified by the number of carbon atoms and functional group they contains.  The monosaccharide glucose is called an Aldohexose as it contains six carbon atoms as well as an aldehyde functional group and fructose is known as ketohexose as it contains six carbons with a ketone functional group.  Similarly, D-threose contain four carbon atom in a chain.

In Killiani-Fisher synthesis, hydrogen cyanide attacks the carbonyl group.  The carbonyl carbon is converted to an asymmetric center.  The CN bond is reduced to an imine which is partially deactivated by palladium catalyst to prevent the reduction of imine to an amine. The two imines are hydrolyzed to two aldoses.

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d-Xylose and d-lyxose are formed when d-threose undergoes a Kiliani–Fischer synthesis. d-Xylose is oxidized to an optically inactive aldaric acid,whereas d-lyxose forms an optically active aldaric acid. What are the structures of d-xylose and d-lyxose?
A D-aldohexose A is formed from an aldopentose B by the Kiliani-Fischer synthesis. Reduction of A with NABH4 forms an optically inactive alditol. Oxidation of B forms an optically active aldaric acid. What are the structures of A and B?
Draw the structure of: (a) a polysaccharide formed by joining D-mannose units in 1→4-β- glycosidic linkages; (b) a polysaccharide formed by joining D-glucose units in 1→6-α- glycosidic linkages. The polysaccharide in (b) is dextran, a component of dental plaque.

Chapter 20 Solutions

Organic Chemistry (8th Edition)

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