Talk:Isoindole
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Both tautomers are aromatic, the one on the left with a 6 pi benzene ring, the one on the right is 10 pi aromatic. So, this page is in error and I have edited it.
Call me stupid, but isn't the pyrrole-like tautomer the one with aromacity around the whole ring system? So shouldn't isoindols chemical properties in solution be more Imine-like, which I doubt? So wouldn't it be right to say the one WITH full aromacity is dominant? But I'm not sure of that and I don't have a heterocycles-textbook around... —Preceding unsigned comment added by 91.47.86.194 (talk) 17:54, 13 May 2008 (UTC)
