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OpenStudy (abhisar):
(Tautomerism Help!) What will be the enol form of following keto compound?
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OpenStudy (abhisar):
This is the given compound|dw:1451915422586:dw|
OpenStudy (abhisar):
I have done it like this |dw:1451915454421:dw|
OpenStudy (abhisar):
Can I do it like this too? |dw:1451915483065:dw|
OpenStudy (abhisar):
@Kainui ?
OpenStudy (kainui):
It can happen that second way but not the major one for sure. it's less stable for I guess at least three reasons or so. It's a terminal alkene, it's not conjugated, and the other spot is just more acidic since it's essentially doubly allylic.
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OpenStudy (abhisar):
Yessss!!! In the first one enol form has H-bonding + Resonance stability. Right?
OpenStudy (kainui):
Yeah I think so
OpenStudy (abhisar):
Thank you <3
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