How would you prepare the following compound using either an acetoacetic ester synthesis or a malonic ester synthesis? Show the reagents, enolate formation, and the flow of electrons. 0 || H₂C=CHCH₂CH₂CCH3
How would you prepare the following compound using either an acetoacetic ester synthesis or a malonic ester synthesis? Show the reagents, enolate formation, and the flow of electrons. 0 || H₂C=CHCH₂CH₂CCH3
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 43AP
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![How would you prepare the following compound
using either an acetoacetic ester synthesis or a
malonic ester synthesis?
Show the reagents, enolate formation, and the flow of
electrons.
O
||
H₂C=CHCH₂CH₂CCH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F67215678-a4aa-4382-ab08-a9c9e76e14df%2F4b13dc3a-364c-490f-8ce5-657291d9feae%2Fwjll8w9_processed.jpeg&w=3840&q=75)
Transcribed Image Text:How would you prepare the following compound
using either an acetoacetic ester synthesis or a
malonic ester synthesis?
Show the reagents, enolate formation, and the flow of
electrons.
O
||
H₂C=CHCH₂CH₂CCH3
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