EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
8th Edition
ISBN: 8220102744127
Author: 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-aldopentose A is reduced to an optically active alditol. Upon Kiliani–Fischer synthesis, A is converted to two D-aldohexoses, B and C. B is oxidized to an optically inactive aldaric acid. C is oxidized to an optically active aldaric acid. What are the structures of A–C?
a) The D-aldopentose A, C5H1005, reacts with HNO3 to yield an optically active aldaric acid B. Kiliani-Fischer chain extension of A produces a pair of D-aldohexoses C and D. C is converted by HNO3 to an optically active aldaric acid, but D is converted by HNO3 to an optically inactive aldaric acid. Write acyclic Fischer projections for A, B, C, D. b) Disaccharide E is a reducing sugar. It is hydrolyzed by an α-glycosidase enzyme, which means it contains an α- glycoside link. Treatment of E with Ag2O and excess Mel gives an octamethyl derivative F. Hydrolysis of F in dilute aqueous acid gives the pair of molecules shown below. Write the structures of E and F. (If the stereochemistry at a particular carbon is not determined by the above data, indicate this with a wavy line as shown below.) HO OMe OMe MeO MeO MOH OMe mOH OMe OMe

Chapter 20 Solutions

EBK ORGANIC CHEMISTRY

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