18. What reagent(s) are suitable to carry out the conversion shown? OH OH A. 1. OsO4, NMO; NaBH4, CH3OH B. 1. 03; 2. (CH3)2S; 3. NaBH4, CH3OH C. 1.03; 2. (CH3)2S. D. Both A and B E. Both B and C

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18. What reagent(s) are suitable to carry out the conversion shown?
OH
OH
A.
1. OsO4, NMO; NaBH4, CH3OH
B. 1. 03; 2. (CH3)2S; 3. NaBH4, CH3OH
C.
1.03; 2. (CH3)2S.
D.
Both A and B
E.
Both B and C
Transcribed Image Text:18. What reagent(s) are suitable to carry out the conversion shown? OH OH A. 1. OsO4, NMO; NaBH4, CH3OH B. 1. 03; 2. (CH3)2S; 3. NaBH4, CH3OH C. 1.03; 2. (CH3)2S. D. Both A and B E. Both B and C
16. Which reaction below gives a single enantiomer of an optically active chiral product?
O
H CH3
||
CH3COOH
A)
HBr
peroxides
1) BH3-THF
2) H,O2, NaOH
HBr
B)
6
H CH3
CH3
CH3
D)
E) None of these
Transcribed Image Text:16. Which reaction below gives a single enantiomer of an optically active chiral product? O H CH3 || CH3COOH A) HBr peroxides 1) BH3-THF 2) H,O2, NaOH HBr B) 6 H CH3 CH3 CH3 D) E) None of these
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