Comparisons of the predictions of stochastic diffusion kinetic calculations using electron track structures with experimental scavenger data show that the precursor to the hydrated electron, e pre -, plays a role in determining the total yield of electrons scavenged in a number of systems. The significance of e pre -scavenging on yields depends on the scavenger of interest and on the rate coefficient of the scavenger's reaction with the hydrated electron, e aq -. For Cd 2+ , where the reaction (e aq -+ Cd 2+ ) is fast, the consequences of e pre -scavenging are experimentally not apparent, for NO 3 -, a less efficient e aq -scavenger, the effects of e pre -reaction are apparent in concentrated solutions, and for SeO 4 2-, an inefficient e aq -scavenger, e pre -scavenging is obvious even in dilute solution.