Extending a problem occurring in connection with the stability order of the
tautomers of hypericin, we examine the topological factors influencing the
stability of the isomeric dioxo derivatives of benzenoid hydrocarbons, in
particular the rules determining the number of Kekule structures in them. D
epending on the position of the oxo groups, the pattern of cyclic conjugati
on varies significantly, as does the Kekule structure count. Some general r
egularities along these lines are established (C) 1999 Elsevier Science B.V
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