Some meta-directing substituents in aromatic substitution are given. Which one is most deactivating?
- $-NO_2$
- $-C = N$
- $-SO_3 H$
- $ -COOH$
The Correct Option is A
Solution and Explanation
${ - NO_2 > -C \equiv N > - SO_3 H > COOH}$
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Concepts Used:
Aromatic hydrocarbon
Aromatic hydrocarbons, sometimes known as arenes, are aromatic organic molecules made up entirely of carbon and hydrogen. In aromatic compounds a benzene ring which is named after the simple aromatic chemical benzene, or a phenyl group when part of a larger structure, is the configuration of six carbon atoms.
Read More: Aromaticity
Reactions of Aromatic Hydrocarbons:
1. Aromatic Substitution Reactions
This reaction involves the replacement of one substituent on the ring of an aromatic hydrocarbon, commonly a hydrogen atom, by a different substituent group.
The common types of aromatic substitution reactions are:
- Nucleophilic aromatic substitution reactions
- Electrophilic aromatic substitution reactions
- Radical nucleophilic aromatic substitution reactions
2. Coupling Reactions
In these types of reactions, the coupling of two fragments that have a radical nature is achieved with the help of a metal catalyst