1. Assign R or S configuration to each stereocenter. H OH (a) H₂C H₂C (b) H CH₂ CH₂CH₂ C-OH CHO (c) H➡C OH CH₂OH

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Organic Chemistry, Ch.4, WS #2, Stereochemistry - Review of R&S configuration, Fischer Projections, Enantiomers,
Diastereomers, Meso Compounds.
1. Assign R or S configuration to each stereocenter.
(a) H₂C
H₂C
a H-
H OH
CH₂CH₂
- Br
CH,
(b)
2. For each Fischer Projection, assign R or S configuration.
CH₂
CH₂CH₂
b. H₂N-
H
COOH
+
-H
CH₂
C-OH (c) HTC OH
CH₂OH
C. Br-
CH₂OH
CI
CHO
CH
Transcribed Image Text:Organic Chemistry, Ch.4, WS #2, Stereochemistry - Review of R&S configuration, Fischer Projections, Enantiomers, Diastereomers, Meso Compounds. 1. Assign R or S configuration to each stereocenter. (a) H₂C H₂C a H- H OH CH₂CH₂ - Br CH, (b) 2. For each Fischer Projection, assign R or S configuration. CH₂ CH₂CH₂ b. H₂N- H COOH + -H CH₂ C-OH (c) HTC OH CH₂OH C. Br- CH₂OH CI CHO CH
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