Phase-boundary-potential-driven ate coupling has been demonstrated for the reaction between hydrophilic arenediazonium ions and lipophilic coupling components in 1,2-dichloroethane (DCE)/water (W) two-phase systems. Instead of using phase-transfer catalysts, hydrophilic arenediazonium ions are driven into the DCE phase by externally controlling the potential drop across the polarized DCE/W interface. The diffusion-controlled transfer of arenediazonium ions across the interface is followed by ate-coupling reactions with coupling components in the DCE phase. The rate of the ate coupling in DCE has been accurately determined by using potential-step chronoamperometry for the transfer for four arenediazonium ions having different lipophilicity in the presence of one of four aromatic coupling components in DCE. No appreciable contribution of the adsorbed reactants to the overall ate-coupling process is detected. An electrochemical approach using liquid/liquid two-phase systems is advantageous in determining the rate of two-phase chemical reactions and is promising for elucidating the mechanism of phase-transfer catalysis.