Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation. Most reactive = 1; if a compound will not react, rank it as "non" rather than assigning a numerical value. Compound A: fluorobenzene Compound B: anisole Compound C: iodobenzene Compound D: bromobenzene

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Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation.
Most reactive
1; if a compound will not react, rank it as "non" rather than assigning a numerical value.
Compound A: fluorobenzene
Compound B: anisole
Compound C: iodobenzene
Compound D: bromobenzene
Transcribed Image Text:Rank each of the following compounds in decreasing order of reactivity towards Friedel-Crafts alkylation. Most reactive 1; if a compound will not react, rank it as "non" rather than assigning a numerical value. Compound A: fluorobenzene Compound B: anisole Compound C: iodobenzene Compound D: bromobenzene
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Friedel Crafts alkylation is the replacement of an aromatic proton with an alkyl group. This happens through electrophilic attack on the aromatic ring with the help of a carbocation. The aromatic ring must be highly nucleophilic i.e. having high electron density to attack the electrophile.

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