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However, HOMA can also be used as a general mol. descriptor appropriate for any type of mol. It reaches the global max. for benzene, whereas the potent magnetic aromaticity NICS index has no lower or upper limits. Hence, questions arise and go beyond mere differences between the geometric and magnetic aspects of aromaticity: (1) Does a mol. of aromaticity greater than that of benzene, but undisclosed by the HOMA definition, exist (2) Can the Kekule cyclohexatriene moiety with HOMA = 0 exist as a part of a larger system (3) Can the geometrical aromaticity index be defined better. Our answer to the first query is \"It is not likely enough\", to the second, \"Why not define HOMA using a less mysterious mol. than cyclohexatriene\", and to the third, \"It is possible to construct another fair geometrical index, but is it better for evaluating aromaticity\" To find these answers, we have studied: (1) the HOMA and NICS indexes of over 50 hexahomosubstituted benzenes, (2) the HOMA, as well as EN and GEO, indexes of over 100 triply fused hexasubstituted benzenes, and (3) the HOMA and new Geometrical Auxiliary Index (GAI) , of different unsatd. and satd., arom. and aliph. hydrocarbons including all alkane constitutional isomers composed of up to nine carbon atoms. 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