Nitration of benzene is a type of electrophilic aromatic substitution reaction in which a nitro group (–NO₂) replaces a hydrogen atom on the benzene ring.
Here’s a simple explanation without equations:
- A mixture of concentrated nitric acid and concentrated sulfuric acid is used to generate the reactive species called the nitronium ion, which acts as the electrophile.
- This nitronium ion attacks the benzene ring, temporarily disrupting its stable electron cloud.
- A hydrogen atom is then removed from the ring, restoring the aromaticity, and the nitro group is attached to the benzene.
Key points:
- The reaction requires strong acids to generate the reactive species.
- The benzene ring remains aromatic after the reaction.
- The product is called nitrobenzene, which is an important intermediate in making dyes, explosives, and pharmaceuticals.