Can Cl2 react with benzene without a catalyst?

Started by Jay0689
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Jay0689

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In destroyer #227, benzene with one amino and one bromine para to each other reacts with Cl2 and H20. The product has one Cl on each side of the NH2 group.

Maybe I'm forgeting my basic reactions, but I thought you needed a catalyst like AlCl3 or UV light to substitute a halogen into a benzene ring.

Can anybody remind me of what I'm missing? thanks!
 
In destroyer #227, benzene with one amino and one bromine para to each other reacts with Cl2 and H20. The product has one Cl on each side of the NH2 group.

Maybe I'm forgeting my basic reactions, but I thought you needed a catalyst like AlCl3 or UV light to substitute a halogen into a benzene ring.

Can anybody remind me of what I'm missing? thanks!

Generally, yes, you need the catalyst. However, amino groups are such powerful activators that a catalyst is not required.