a. Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. On the structures provided below, formation of an enamine from cyclopentanone and piperidine. draw the curved arrows for the reaction mechanism for the acetic acid-catalyzed H H H H O O N H H H3C- isan (PT) 000 H 19184 Proton Transfer H- —0: HY : :O-H PHO food to shufourte sitt allarW m H H 828-- H H 12.H H HO: Ni

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a.
Enamines formed from the cyclic secondary amine pyrrolidine are important
intermediates in the synthesis of 1,5-diketones. On the structures provided below,
formation of an enamine from cyclopentanone and piperidine.
draw the curved arrows for the reaction mechanism for the acetic acid-catalyzed
H
H
H
H
eo N
H
H
H3C-
isod
1916w
Proton Transfer
(PT)
000
'H
HO
:01H
SHO
6:
HO
H
H
8²8--
H
H
12.H
food to shujounte sitt allarWm
H
OH M
HO N
Transcribed Image Text:a. Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. On the structures provided below, formation of an enamine from cyclopentanone and piperidine. draw the curved arrows for the reaction mechanism for the acetic acid-catalyzed H H H H eo N H H H3C- isod 1916w Proton Transfer (PT) 000 'H HO :01H SHO 6: HO H H 8²8-- H H 12.H food to shujounte sitt allarWm H OH M HO N
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