The conversion of ethylchloride into ethylene + HCl on pure and doped alumina supports and on CuCl2-Al2O3-based oxychlorination catalysts has been investigated by pulse reactor and FT-IR spectroscopy. FT-IR spectra of ethylchloride adsorbed on gamma -Al2O3 show weakly molecularly adsorbed species and ethoxy groups formed by nucleophilic substitution, Additionally, adsorbed diethylether is also observed. The analysis of the gas-phase species shows that ethoxy groups decompose, giving rise to ethylene at 523 K, Under the same conditions, gaseous HCl is also released from the surface and diethylether is also observed in the gas phase. Chlorination of alumina with HCl only partially hinders the dehydrochlorination mechanism occurring through ethoxy groups. Experiments performed on alumina doped with MgCl2 and KCI indicate that the site reactivity scale for EtCl conversion to ethylene is the following: bare Al2O3 > CuCl2 on Al2O3 > MgCl2 on Al2O3 > KCl on Al2O3 Doping with MgCl2 and in particular with KCl limits the activity of the bare support in the dehydrochlorination, These data strongly support the previous proposal that the exposed alumina surface catalyzes the dehydrochlorination of EDC to VCM, with a consequent loss in selectivity in the oxychlorination reactor. The beneficial effect of doping with KCl and MgCl2 is due to the reduced dehydrochlorination activity.