Can Cl2 react with benzene without a catalyst?

This forum made possible through the generous support of SDN members, donors, and sponsors. Thank you.

Jay0689

Full Member
10+ Year Member
Joined
Apr 16, 2011
Messages
35
Reaction score
0
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.
 
Thanks for the help! I'll add that to my growing list of reactions I never knew about until doing destroyer.
 
Top