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why does a shift occur from keto to enol form in tautomerism even though keto form is more stable than enol form?
Reasons are: Aromaticity –> with -OH group attached to benzene enables the phenol to attain the stability. Hydrogen Bonding-> OH group has tendency to make H-Bonding with water. Type of solvent → with polar protic solvent lone pairs would be available for H- Bonding.
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