Toluene reacts as a normal aromatic hydrocarbon in electrophilic aromatic substitution.Because the methyl group has greater electron-releasing properties than a hydrogen atom in the same position, toluene is more reactive than benzene toward electrophiles. It undergoes sulfonation to give p-toluenesulfonic acid, and chlorination by Cl2 in the presence of FeCl3 to give ortho and para isomers of chlorotoluene.
Property Value | |
Chemical Name | Toluene |
InChI | 1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3 |
Smile String | Cc1ccccc1 |
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