pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)

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Chapter9: Ionic And Covalent Bonding
Section: Chapter Questions
Problem 9.112QP
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Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)
e
:0:
TÖ:
H
H* transfer
d P-8²8²-
H₂O* +
- &
H
H₂O
HÖ: N
11
H₂O:
H-OAc
Transcribed Image Text:e :0: TÖ: H H* transfer d P-8²8²- H₂O* + - & H H₂O HÖ: N 11 H₂O: H-OAc
8.8= 8.-
'N
+ H₂O
H
HOAc
Transcribed Image Text:8.8= 8.- 'N + H₂O H HOAc
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