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- Apr 27, 2008
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I have a question regarding polyhalogenation. When benzene is treated w/ Ch3 or any alkyl group it should activate the ring right. B/C CH3- groups are ortho/para activators. So if the new activated ring is now treated w/ a halogen like Br souldn't it go through polyhalogenation at every o/p position on the ring? Or does it stop after only 1 Br in the ortho position as the minor product and 1 Br as para as the major product b/c halogens will decativate the ring? If this is the case when does polyhalogenation occur in general?