Chapter 28: Question 28.40 (page 1147)
Convert each compound to a Fischer projection and label each stereogenic center as R or S.
(a.)
(b.)
(c.)
(d.)
(e.)
(f.)
Short Answer
Answer
(a.)
(b.)
(c.)
(d.)
(e.)
(f.)
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Chapter 28: Question 28.40 (page 1147)
Convert each compound to a Fischer projection and label each stereogenic center as R or S.
(a.)
(b.)
(c.)
(d.)
(e.)
(f.)
Answer
(a.)
(b.)
(c.)
(d.)
(e.)
(f.)
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What two aldoses yield D-xylose on Wohl degradation?
a. Identify the glycosidic linkage in disaccharide C, classify the glycosidic bond as , and use numbers to designate its location.
b. Identify the lettered compounds in the following reaction.

Draw a Haworth projection for each compound using the structures in Figures 28.4 and 28.5.

Draw the products formed when D-arabinose is treated with each reagent. (a) ; (b) ; (c) ,
A D-aldohexose A is formed from an aldopentose B by the Kiliani-Fischer synthesis. Reduction of A with forms an optically inactive alditol. Oxidation of B forms an optically active aldaric acid. What are the structures of A and B?
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