Why is the overacylation of benzene not a problem when subjecting benzene to a Friedel-Crafts acylation reaction? The product is higher in energy than the reactant, making it stable and unable to react further There is not enough catalyst to allow another acylation The product is too sterically hindered to undergo another acylation reaction The product of the reaction is deactivated compared to the starting material

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter19: Enolate Anions And Enamines
Section: Chapter Questions
Problem 19.82P: The following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium...
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Why is the overacylation of benzene not a problem when subjecting
benzene to a Friedel-Crafts acylation reaction?
The product is higher in energy than the reactant, making it stable and unable to
react further
There is not enough catalyst to allow another acylation
The product is too sterically hindered to undergo another acylation reaction
The product of the reaction is deactivated compared to the starting material
Transcribed Image Text:Why is the overacylation of benzene not a problem when subjecting benzene to a Friedel-Crafts acylation reaction? The product is higher in energy than the reactant, making it stable and unable to react further There is not enough catalyst to allow another acylation The product is too sterically hindered to undergo another acylation reaction The product of the reaction is deactivated compared to the starting material
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