MAYB NOT
ACTIVATOR WINS OVER DEACTIVATOR SO SHUD BE ORTHO TO CH3 but not b/w NO2 n CH3, on the other side...
ans kya hai?
MAYB NOT
ACTIVATOR WINS OVER DEACTIVATOR SO SHUD BE ORTHO TO CH3 but not b/w NO2 n CH3, on the other side...
ans kya hai?
See the intermediate formed can have 2 structures:-
and correspondingly following products can be obtained
Also there is carbanion formation in between so that structure will be favoured which is obtained from most stable carbanion...
In my view the NH2 will be at place of Cl cause NO2 group is -I group hence it can stabilise the carbanion formed but on the other hand it is also a deactivating group.
i just thought dat as m effect dominate over H n I Effect so it ll be favoured to get rid o f -m of no2