Greetings,
my question pertains to counting the pi electrons(N) for Huckel's rule of aromaticity...
Is it correct to just count the carbons on each double bond...
or
do i count the sides up on the whole structure.
I understand that that for it to be aromatic you use the 4N+2 and for it to be anti armatic 4N
I also unstand for it to be armatic
it has to be cyclic, and conjugated.. It has to sp2 or sp hybridized...planar...low state of energy