1-Hexyne is treated with sodium hydride, followed by bromoethane. Lindlar hydrogenation of the resulting product afforas final product? 1) NaH H2 2) CH3CH2Br Lindlar's catalyst C (E)-3-octene C (E)-2-octene (Z)-3-octene C (Z)-2-octene

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 9.60P: Another important pattern in organic synthesis is the construction of CC bonds. Using your reaction...
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1-Hexyne is treated with sodium hydride, followed by bromoethane. Lindlar hydrogenation of the resulting product affords what
fınal product?
1) NaH
H2
?
2) CH3CH2B1
Lindlar's catalyst
C (E)-3-octene
(E)-2-octene
C (Z)-3-octene
C (Z)-2-octene
Transcribed Image Text:1-Hexyne is treated with sodium hydride, followed by bromoethane. Lindlar hydrogenation of the resulting product affords what fınal product? 1) NaH H2 ? 2) CH3CH2B1 Lindlar's catalyst C (E)-3-octene (E)-2-octene C (Z)-3-octene C (Z)-2-octene
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