Either enantiomer of the SULFOXIDE below may be prepared from (S)-2-butanol. Propose an efficient synthesis of each enantiomer from (S)-2-butanol using any additional reagents of your choice. SCH,CH3 OH SCH,CH3

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter9: Nucleophilic Substitution And Β-elimination
Section: Chapter Questions
Problem 9.41P: Elimination of HBr from 2-bromonorbornane gives only 2-norbornene and no 1-norbornene. How do you...
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Either enantiomer of the SULFOXIDE below may be prepared from (S)-2-butanol. Propose an
efficient synthesis of each enantiomer from (S)-2-butanol using any additional reagents of your choice.
SCH,CH3
OSCH,CH3
Transcribed Image Text:Either enantiomer of the SULFOXIDE below may be prepared from (S)-2-butanol. Propose an efficient synthesis of each enantiomer from (S)-2-butanol using any additional reagents of your choice. SCH,CH3 OSCH,CH3
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