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Reinvestigation of the Deceptively Simple Reaction of Toluene with OH and the Fate of the Benzyl Radical: The “Hidden” Routes to Cresols and Benzaldehyde

Zoi Salta, Agnie M. Kosmas, Marc E. Segovia, Martina Kieninger, Nicola Tasinato, Vincenzo Barone, Oscar N. Ventura

2020The Journal of Physical Chemistry A32 citationsDOIOpen Access PDF

Abstract

-cresol were determined. Moreover, in this situation, the benzyl radical is predicted to produce benzyl alcohol, as was found in some experiments. The commonly accepted route to benzaldehyde was found to be not the energetically favored one. Instead, a route leading to the benzoyl radical (and ultimately to benzoic acid) with the participation of one water molecule was clearly more favorable, both thermodynamically and kinetically.

Topics & Concepts

ChemistryRadicalBenzaldehydeHydroperoxylToluenePhotochemistryBenzyl alcoholHydrogen atom abstractionReactivity (psychology)Hydroxyl radicalComputational chemistryMedicinal chemistryCatalysisOrganic chemistryPathologyMedicineAlternative medicineFree Radicals and AntioxidantsAtmospheric chemistry and aerosolsCatalysis and Oxidation Reactions
Reinvestigation of the Deceptively Simple Reaction of Toluene with OH and the Fate of the Benzyl Radical: The “Hidden” Routes to Cresols and Benzaldehyde | Litcius