rwy’:4 :77“, CH M235lN — ln-class, Ch 5 Stereoisomers Due 10/09/17 4. Convert each perspective drawing and Newman projection below into a Fischer (bowtie) projection, (5 pts) 5. Convert each Fischer projection below into a perspective drawing. (4 pts) OH H +Br CH3 CHZOH el—l—H CH3 6. For (a) through (0) below, which of the following terms best describes the pair of compounds shown: same or different stereoisomer? (2 pts) (8) CH3 COOH H/R’WCOOH H2N+H NH2 CH3 (b) Br CH3 H c/kWH H+Br 3 CHZCHa CH2CH3 ‘ / 11

rwy’:4 :77“, CH M235lN — ln-class, Ch 5 Stereoisomers Due 10/09/17 4. Convert each perspective drawing and Newman projection below into a Fischer (bowtie)
projection, (5 pts) 5. Convert each Fischer projection below into a perspective drawing. (4 pts) OH H +Br CH3 CHZOH el—l—H CH3 6. For (a) through (0) below, which of the following terms best describes the pair of compounds
shown: same or different stereoisomer? (2 pts) (8)
CH3 COOH
H/R’WCOOH H2N+H
NH2 CH3
(b)
Br CH3 H c/kWH H+Br
3 CHZCHa CH2CH3
‘ / 11

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