Whats the difference btw non-aromatic, and antiaromatic?
to be an aromatic it has to be planar and follow huckel's 4n+2 rule, but what is an antiaromatic? I know its different than a non-aromatic, but I cant find a good clarification btw the two...
Whats the difference btw non-aromatic, and antiaromatic?
to be an aromatic it has to be planar and follow huckel's 4n+2 rule, but what is an antiaromatic? I know its different than a non-aromatic, but I cant find a good clarification btw the two...
Whats the difference btw non-aromatic, and antiaromatic?
to be an aromatic it has to be planar and follow huckel's 4n+2 rule, but what is an antiaromatic? I know its different than a non-aromatic, but I cant find a good clarification btw the two...
Non Aromatic: Are not Planar, though they may be conjugated and have 4n+2 pi electrons
Antiaromatic: Has 4n pi electrons, may also be conjugated and cyclic, also planar
Easiest way is to just count the double bonds as 2 pi electrons...benzene is cyclic, planar and has 6 pi elec. (4(2) + 2).....If you have an 8 sided cyclic conjugated ring, it will have 8 pi electrons (2*4 dbl bonds) which is does not fit 4n+2, but it does fit 4n...however it is not planar....dont forget to count lone pair electrons too....Im sure that there will be one of these questions on the DAT...I see it everywhere!