Abstract
Studies of bond dissociation energies of organic polyatomic molecules led me to conclude that the weakest bond in toluene is the PhCH2-H. Indeed, pyrolysis of toluene carried out in a flow system at pressures of 5–10 torrs resulted in its dissociation into a thermally stable benzyl radical and a hydrogen atom1. Thus, dibenzyl and H2 were the main products of the decomposition.
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Ulrich, R.D. (1978). M. Szwarc. In: Ulrich, R.D. (eds) Macromolecular Science. Contemporary Topics in Polymer Science, vol 1. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-2853-7_17
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