The hydrogenation of crotonaldehyde was conducted in gaseous phase, at atmospheric pressure, on Pt/CeO2 catalysts prepared from metal precursors containing or not chlorine. The activities and selectivities were studied, at 253 K, as a function of the reduction temperature of the catalyst (473-993 K). The Pt/CeO2 catalyst, prepared from tetraammineplatinum nitrate, led to 5-20% crotyl alcohol selectivity when the catalyst was reduced at low temperature (473-673 K), while increasing the reduction temperature up to 973 K, the crotyl alcohol selectivity reached more than 80%. Repeating a series of experiments after a re-calcination treatment at 673 K, the selectivity decreased to only 40% after 473 K reduction to reach again more than 80% after 673 K reduction temperature. A phase transformation of Pt to CePt5 was observed by XRD analysis after 973 K reduction treatment. Differently on Pt/CeO2 catalysts containing chlorine, prepared from either chloroplatinic acid or tetraammineplatinum chloride, the crotyl alcohol selectivity never exceeded 30% and did not form alloy up to 973 K reduction temperature. The main results are interpreted considering that the activity of CePt5 for C=C hydrogenation is low compared to unmodified platinum catalyst and the activation of the carbonyl bond is induced by the presence of oxygen vacancies sites located at the interface between ceria and the metallic particles. The results are in good accordance with the information known at the present time on the metal-support interactions in Pt deposited on CeO2.