Measurements of the influence of reactant alignment on the rates of ch
emical reactions provide direct information concerning the atomic moti
ons necessary for chemical transformation. Data presented here show th
at at low collision energy, the dissociative adsorption of deuterium (
D-2) on the (111) surface of copper has a much higher probability for
broadside than for end-on collisions. Furthermore, this steric prefere
nce is sensitive to the kinetic energy of the incident molecule, almos
t disappearing as the energy increases to 0.8 electron volt. This stud
y shows that the dynamic conditions of a surface chemical reaction can
profoundly influence the associated steric requirements.