Nonconjugated β,γ-unsaturated ketones are in base-catalyzed equilibrium with their conjugated α,β-unsaturated isomers. The mecha
nism of interconversion involves the formation of a resonance-stabilized intermediate with three resonance contributors. Draw the structures of these three resonance contributors.
1 answer:
Answer:
Explanation:
The equilibrium mechanism for the reversible acid is catalyzed by the isomerization of non conjugated β, γ- unsaturated ketones, like 3-cyclohexanone to their conjugated α, I²- unsaturated isomers.
Oxygen of the Carbonyl group in the ketone is protonated by the acid and this is followed by the abstraction of an α- hydrogen from the protonated 3-cyclo hexanone to yield ethanol
2-cyclo hexanone can be obtained by acid catalyzation of 3-cyclohexanone isomers through the formation of it's "enol".
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Answer:
use the formula above it's easy
