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on a ring with two substituents, an activating and a deactivating group on a benzene molecule...is there a general rule that says that the activating group is more influential in directing the substituent to the correct place over the deactivating?
I recall a problem where i believe there was a deactivating group and para to that was an activating group..and the substituent was placed meta to the deactivating group (or ortho to the activating group)
I recall a problem where i believe there was a deactivating group and para to that was an activating group..and the substituent was placed meta to the deactivating group (or ortho to the activating group)
