The Fischer projection of the branched-chain carbohydrate D-apiose has been presented in Section 25.12 (a) How many
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(a) How many stereogenic centers are in the open-chain form of D-apiose?
(b) Does D-apiose form an optically active alditol on reduction?
(c) How many stereogenic centers are in the furanose forms of D-apiose?
(d) How many stereoisomeric furanose forms of D-apiose are possible? Write their Haworth formulas.
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a Carbon2 is the only stereogenic center in Dapiose Carbon3 is not a stereogenic center it bears two ...View the full answer
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