Study the reaction scheme shown below and answer all sections (i) – (v) relating to it. ? Na* EC ? Br H F Reaction of alkyne D with a strong base gave an intermediate E, which reacted with compound F to give product G. Suggest a base that could be used in this reaction, and explain why the hydrogen that is removed is unusually acidic compared to other H atoms bonded to carbon. Propose a reagent and catalyst to accomplish the conversion of compound G into alkane H.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter9: Addition Via Cyclic Intermediate
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Study the reaction scheme shown below and answer all sections (i) – (v) relating to it.
?
EC Na*
?
E
Br
H
F
Reaction of alkyne D with a strong base gave an intermediate E, which reacted with compound
F to give product G. Suggest a base that could be used in this reaction, and explain why the
hydrogen that is removed is unusually acidic compared to other H atoms bonded to carbon.
Propose a reagent and catalyst to accomplish the conversion of compound G into alkane H.
Transcribed Image Text:Study the reaction scheme shown below and answer all sections (i) – (v) relating to it. ? EC Na* ? E Br H F Reaction of alkyne D with a strong base gave an intermediate E, which reacted with compound F to give product G. Suggest a base that could be used in this reaction, and explain why the hydrogen that is removed is unusually acidic compared to other H atoms bonded to carbon. Propose a reagent and catalyst to accomplish the conversion of compound G into alkane H.
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