Abstract Using classical molecular dynamics, we have investigated the solvation of catechol, resorcinol, hydroquinone and 1,4‐benzoquinone at infinite dilution, in a series of menthol ‐ thymol mixtures in which the molar fraction of thymol (x THY ) has been increased by steps of 0.1, from 0 ( pure menthol ) to 1 ( pure thymol ). The evolution of the solvation shell around the solutes reveals that when x THY is increased, the average number of hydrogen bonds (HB) where the solute acts as HB acceptor (HBA) and the solvent as HB donor (HBD) increases, while the amount of HB, in which the solute acts as HBD and the solvent as HBA, decreases. Overall, the total number of HBs between the different benzenediols and the solvent decreases with an increase of x THY , while for benzoquinone the total number of HB increases. This points to the fact that “acidic” or HBD molecules are better solvated in mixtures with high menthol proportion, while “basic” or HBA molecules, are better solvated in thymol rich mixtures. The results reported herein follow the same trends as experimentally reported Kamlet‐Taft parameters and present insights on how the composition of these “deep eutectic” mixtures maybe tweaked in order to optimize their solvation properties.