Many hydrocarbons involve hexagonal rings; benzene, consisting of a single hexagon of carbons with hydrogens attached, is the original example. It turns out that the number of perfect matchings in certain associated graphs is relevant to the chemistry of these hydrocarbons. Furthermore, standard methods of undergraduate linear algebra and discrete mathematics can be used to count the matchings, and familiar counting numbers show up. In this article we present this easily accessible but seemingly little known connection between chemistry and mathematics. According to the chemistry folklore, the German chemist August Kekule (18291896) discovered the molecular structure of benzene after he dreamed of a snake swallowing its own tail. Apparently, the dream led to his conjecture that benzene consists of 6 carbon atoms, each linked to 1 hydrogen atom via a carbon-hydrogen bond, and that the carbon atoms are linked to each other via a cycle of length 6 consisting of alternating single and double carbon-carbon bonds. FIGURE 1 illustrates a molecular model of benzene. Kekule's discovery initiated the study of special types of graphs used to model benzene-like molecules called benzenoids.
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