What was the starting alkyne and the corresponding reagents for the formation of (this is acetylide formation): CH;CH2CH2C=c-H A H-C=C-H and NaNH2, NH3, CH;CH2B H-C=C-H and NaNH2, NH3, CH;CH2CH2CH2B H-C=C-H and NaNH2, NH3 , CH;CH2CH,Br Н—СС—H and NaNH2, NH3, CH CH2CH2CH-CH-Br
What was the starting alkyne and the corresponding reagents for the formation of (this is acetylide formation): CH;CH2CH2C=c-H A H-C=C-H and NaNH2, NH3, CH;CH2B H-C=C-H and NaNH2, NH3, CH;CH2CH2CH2B H-C=C-H and NaNH2, NH3 , CH;CH2CH,Br Н—СС—H and NaNH2, NH3, CH CH2CH2CH-CH-Br
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 9.39P: Following are diastereomers (A) and (B) of 3-bromo-3,4-dimethylhexane. On treatment with sodium...
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![What was the starting alkyne and the corresponding reagents for the formation of (this is acetylide formation):
CH;CH2CH2C=C-H
H-C=C–H and NaNH2, NH3 , CH3CH2Br
B
H-C=C–H and NaNH2, NH3 , CH;CH2CH2CH2B.
H-C=C-H and NaNH2, NH3, CH3CH2CH,Br
D
Н—СЕС—H and NaNH2, NH3, CH;CH2CH2CH,CH,Br](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3cebbc4c-7d5a-45fc-9bec-fe7b8f7c2124%2F810a389d-1e3d-4157-93f2-365e6958642a%2Fwe4ounh_processed.png&w=3840&q=75)
Transcribed Image Text:What was the starting alkyne and the corresponding reagents for the formation of (this is acetylide formation):
CH;CH2CH2C=C-H
H-C=C–H and NaNH2, NH3 , CH3CH2Br
B
H-C=C–H and NaNH2, NH3 , CH;CH2CH2CH2B.
H-C=C-H and NaNH2, NH3, CH3CH2CH,Br
D
Н—СЕС—H and NaNH2, NH3, CH;CH2CH2CH,CH,Br
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