Destroyer Roadmap question plz....

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

whawha

Full Member
10+ Year Member
Advertisement - Members don't see this ad
If ethylbenzene is treated with Br2/uv, we get a bromine on the benzylic carbon, right?

If it is treated with NBS, ROOR and heat, aren't we supposed to have the bromine on the second carbon (btw, what is that carbon called?)

I remember a question where it was saying, NBS,ROOR would attach bromine to allylic position, say if you have a cyclohexene.

Am i missing something?
 
If ethylbenzene is treated with Br2/uv, we get a bromine on the benzylic carbon, right?

If it is treated with NBS, ROOR and heat, aren't we supposed to have the bromine on the second carbon (btw, what is that carbon called?)

I remember a question where it was saying, NBS,ROOR would attach bromine to allylic position, say if you have a cyclohexene.

Am i missing something?

As I recall, NBS/ROOR will attach Br to the benzyllic carbon just like Br2/hv.
 
But, if you have peroxide, doesn't it normally follow Anti-markovnikov rule? So, bromine attached on less stable carbocation, which is C2 in the compound above?

I think the peroxides are just added as initiators for free radical bromination. Pretty much whenever you see NBS with alkyl benzenes, Br is selectively substituted at the benzyllic carbon.