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Questions and Answers
Which step in the halogenation of benzene is considered the rate-determining step?
Which step in the halogenation of benzene is considered the rate-determining step?
What is the role of the catalyst in the Friedel-Crafts Alkylation reaction?
What is the role of the catalyst in the Friedel-Crafts Alkylation reaction?
Which species acts as a Lewis acid in the halogenation mechanism?
Which species acts as a Lewis acid in the halogenation mechanism?
What is the product of nitration of nitrobenzene?
What is the product of nitration of nitrobenzene?
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What is the purpose of H2SO4 in the sulphonation of benzene?
What is the purpose of H2SO4 in the sulphonation of benzene?
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What is the major disadvantage of Friedel-Crafts alkylation with respect to polyalkylation?
What is the major disadvantage of Friedel-Crafts alkylation with respect to polyalkylation?
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Which step involves the formation of a σ Complex during SE aromatic substitution?
Which step involves the formation of a σ Complex during SE aromatic substitution?
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Why do benzene rings with strong deactivating groups like NO2, SO3H, CHO, or COOH not undergo Friedel-Crafts alkylation?
Why do benzene rings with strong deactivating groups like NO2, SO3H, CHO, or COOH not undergo Friedel-Crafts alkylation?
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In Friedel-Crafts alkylation, what leads to the rearrangement of the alkyl group?
In Friedel-Crafts alkylation, what leads to the rearrangement of the alkyl group?
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One advantage of Friedel-Crafts acylation over alkylation is:
One advantage of Friedel-Crafts acylation over alkylation is:
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What is a common drawback of Friedel-Crafts alkylation when dealing with NH2, NHR, or NR2 substituted benzene rings?
What is a common drawback of Friedel-Crafts alkylation when dealing with NH2, NHR, or NR2 substituted benzene rings?
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What effect does the +I effect of CH3 group have in Friedel-Crafts alkylation?
What effect does the +I effect of CH3 group have in Friedel-Crafts alkylation?
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