Organic Chemistry&mod Mstg Etx Vp Ac Pkg
Organic Chemistry&mod Mstg Etx Vp Ac Pkg
1st Edition
ISBN: 9780134466729
Author: Bruice
Publisher: Pearson Education
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Chapter 20, Problem 46P
Interpretation Introduction

Interpretation:

The hexose obtained after three successive Killiani-Fisher synthesis of (+)-glyceraldehyde is to be predicted on the basis of given information.

Concept Introduction:

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?
Which D-aldopentose is oxidized to an optically active aldaric acid and undergoes the Wohl degradation to yield a Daldotetrose that is oxidized to an optically active aldaric acid?
An unknown β-d-aldohexose has only one axial substituent. A Wohl degradation forms a compound which, when treated with sodium borohydride, forms an optically active alditol. This information allows you to arrive at two possible structures for the β-d-aldohexose. What experiment can you carry out to distinguish between the two possibilities?

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Organic Chemistry&mod Mstg Etx Vp Ac Pkg

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