The process whereby a hydrogen atom attached to the alpha-carbon carbonyl compound moves to the cabonyl oxygen atom is nown as enolization or keto-enol tautomerism. Isomeric carbonyll and enol structures are tautomers. Normally, the carbonyll form is favoured but structural factor market affect K_(T). Which of the following does not exits in enol forms?

The process whereby a hydrogen atom attached to the alpha-carbon carbo

1.	The process whereby a hydrogen atom attached to the alpha-carbon carbonyl compound moves to the cabonyl oxygen atom is nown as enolization or keto-enol tautomerism. Isomeric carbonyll and enol structures are tautomers. Normally, the carbonyll form is favoured but structural factor market affect K_(T). Which of the following does not exits in enol forms?
Answer» `CH_(3)-overset(O)overset(\|\|)(C)-C-UNDERSET(O)underset(\|\|)(C)-CH_(3)` `CH_(3)-overset(O)overset(\|\|)(C)-CH_(2)-overset(O)overset(\|\|)(C)-CH_(3)` SOLUTION :Transitoid form is stable Can't for INTERMOLECULAR its bond