2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) is a promising, sustainable, metal-free mediator for oxidation of alcohols. In this contribution, we describe how the selectivity of TEMPO for electrocatalytic alcohol oxidations in room-temperature ionic liquids (RTILs) can be changed by design of the solvent medium. Cyclic voltammetry of TEMPO in a series of ammonium-, phosphonium-, and imidazolium-based RTILs reveals that the potential at which TEMPO is oxidized increases from 677 mV (vs. the potential of the decamethylferrocene/ decamethylferrocinium, dmFc/dmFc + , redox couple) to 788 mV as the H-bond basicity of the RTIL anions decreases. The increase in potential is accompanied by an increase in the rate constant for oxidation of benzyl alcohol from about 0.1 dm 3 mol −1 s −1 to about 0.7 dm 3 mol −1 s −1 , demonstrating the ability to manipulate the reactivity of TEMPO by judicious choice of the RTIL anions. The rate of alcohol oxidation in a series of RTILs increases in the order 2-butanol < 1phenylethanol < octanol < benzyl alcohol, and the RTIL 1-octyl-3-methylmidazolium bis(trifluoromethanesulfonyl)imide ([NTf2] -) shows clear selectivity towards the oxidation of primary alcohols. In addition, the reaction kinetics and selectivity are better in [NTf2] --based RTILs than in acetonitrile, often the solvent-of-choice in indirect alcohol electrooxidations.Finally, we demonstrate that electrolytic TEMPO-mediated alcohol oxidations can be performed using RTILs in a flow-electrolysis system, with excellent yields and reaction selectivity, demonstrating the opportunities offered by such systems.