The kinetics of oxidation of Ethylenediammine-N,N,N',N'-tetraacetatocobaltate(II) complex (()) by silver-activated persulphate ion in a ueous nitric acid medium was studied at I = 0.5 mol dm-3 (NaNO3), [H + ] = 1 × 10-2 mol dm-3 , [Ag + ] = 1 × 10-2 mol dm-3 , T = 299 ± 1 K and λmax = 520 nm. Stoichiometric study showed 2:1 (Reductant: Oxidant) mole ratio. The reaction exhibited first order with respect to the [Co(II)EDTA 2-] and [ 2 8 2 O S ] and the rate constant, (5.90 × 10-2 dm 3 mol-1 s-1) was independent of the acid concentration, but varied linearly with catalyst concentration, [Ag + ]. The overall rate law is represented as: () () The reaction displayed zero salt effect suggesting an activated complex composed of either a neutralcharged, neutral-neutral reactant species or ion-pair. The reaction was catalysed by addition of formate ion, HCOOand the Michaelis-Menten's type plot gave zero intercept indicating the absence of intermediate complex. Also, the activation enthalpy (= +39.27 kJ mol-1) and entropy (=-136.73 J K-1 mol-1) were determined. The entropy of activation shows a more ordered activated complex relative to the reactants species. Evaluating the experimental data, an outer-sphere mechanistic pathway via ion pair activated complex is proposed for the reaction.