Non-conjugated β, γ-unsaturated ketones, such as 3-cyclohexenone, as in base-catalyzed equilibrium with their α,β-unsaturated is
omers. An interesting consequence of this isomerization of unsaturated ketones is that 2-substituted cyclopentenones, such as 2-methyl-2-cyclopentenone, can be interconverted with 5-substituted 2-cyclopentenones. The first intermediate in this reaction has three resonance structures.
Draw all resonance structures for the first intermediate in the conversion of 2-methyl-2-cyclopentenone to 5-methyl-2-cyclopentenone.
Draw all resonance structures for the first intermediate in the conversion of 2-methyl-2-cyclopentenone to 5-methyl-2-cyclopentenone.
1 answer:
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825.5mL
To find this, use the equation =
Make sure to convert all temperatures in Celsius to Kelvin by adding 273. Once you do that, multiply and divide accordingly to get the final answer of 825.5mL
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