3rong ans sir
14 Answers
1I am not too sure but i feel C should be the ans....as in A and B an aromatic ion with a pair of pi electrons will be there...whereas in C an anti aromatic species will be formed....
3sidsgr88 there is another choice in the question which also yields an anti aromatic ion but it is not the correct ans da
1i think that if positive charge develops on carbon of cyclic compound in option (b) then the carbon will be become sp2 hybridised i.e. angle is 120° ,so there will be angle strain.....
just a wild guess.....
3can u explain abt the option a)
can u explain with mech for ur reason.i cant get u y +ive charge develops on the carbon
3i am posting the answers people please give me the mech for the products please please
1thats what i was saying sankara.....in a,c,d an electrophile is added so that a carbocation is formed...then the intermediate may b classified as stable of unstable....in b two nucleophiles are removed to make it an aromatic species...