
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Complete the following reactions of the compound shown by drawing the correct products with correct steriochemistry if important


Transcribed Image Text:1.OsO
NaHSO3
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- Please don't provide handwritten solution ....arrow_forwardRibose, a carbohydrate with the formula shown, forms a cyclic hemiacetal, which, in principle, could contain either a four-membered, five-membered, or six-membered ring. When D-ribose is treated with methanol in the presence of an acid catalyst, two cyclic acetals, A and B, are formed, both with molecular formula C,H,0, These are separated, and each is treated with sodium periodate (Section 10.8C) followed by dilute aqueous acid. Both A and B yield the same three products in the same ratios. он о CHO СНО H+ CH,OH A +B ÕH 1. NalO, 2. H,0* НО CHO + CHOH + CH,OH ÕH CH,OH Isomeric cyclic acetals with molecular formula CH12O, D-Ribose (C;H1605) From this information, deduce whether the cyclic hemiacetal formed by D-ribose is four- membered, five-membered, or six-membered.arrow_forwardDraw all stereoisomers for ethyl 2,4-diphenyl-3-oxobutanoatearrow_forward
- (1) what reagent is used to convert p-amino phenol to quinone (2) Draw two different kekule's structures for pyrene and under line the more stablearrow_forwardDraw the condensation product of (R)-2-(2-oxopropyl)cyclopentanonearrow_forwardgive the IUPAC names for the following compound: specify stereochemistry if relevantarrow_forward
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