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:
It traveled 4 centimeters.
Explanation:
In a speed versus time graph, the distance travelled is given by the area under the graph.
In this graph we have the following:
- The speed of the object is v = 1 cm/s between time t = 0 s and t = 4 s
- The speed of the object is v = 0 cm/s between time t = 4 s and t = 8 s
Since the speed in the second part is zero, the distance travelled in the second part is zero. So, the only distance travelled by the object is the distance travelled during the first part, which is equal to the area of the first rectangle: