Asked by atilola akeem on May 10, 2024

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The nitration of anisole ________.

A) proceeds more rapidly than the nitration of benzene and yields predominantly the meta product
B) proceeds more rapidly than the nitration of benzene and yields predominantly the ortho, para products
C) proceeds more slowly than the nitration of benzene and yields predominantly the meta product
D) proceeds more slowly than the nitration of benzene and yields predominantly the ortho, para products
E) proceeds at the same rate as the nitration of benzene and yields predominantly the meta product

Nitration

A chemical reaction that introduces a nitro group (NO2) into an organic compound, usually involving the substitution of an H atom, often used to synthesize explosives or other nitro compounds.

Anisole

An organic compound consisting of a methoxybenzene group, used as a precursor in the synthesis of other chemicals.

Ortho

In chemistry, a designation used in nomenclature to indicate adjacent or 1,2- substitution in the structure of benzene ring compounds.

  • Explore the effects of activating and deactivating groups on the kinetics and orientation of electrophilic aromatic substitution reactions.
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ZK
Zybrea KnightMay 15, 2024
Final Answer :
B
Explanation :
Anisole has electron-donating -OCH3 group which activates the benzene ring towards electrophilic substitution. This makes nitration occur more rapidly than benzene. Additionally, the -OCH3 group is ortho, para directing, leading to the formation of predominantly ortho and para products.