In the present work studies were made on the deuteration of cyclohexad
iene over reduced and sulfided molybdena-alumina. The deuteration reac
tion goes in two steps. At first cyclohexene is formed and this is fur
ther hydrogenated to cyclohexane. The formation of cyclohexadiene-d4 c
an be explained by equal exchange in the four vinyl positions of cyclo
hexadiene over the coordinatively unsaturated sites of the molybdena.
The sulfied molybdena-alumina exhibited a much lower hydrogenation rat
e for the cyclohexadiene.