Many photochemical processes involving the breaking and formation of chemic
al bonds take place on a femtosecond time scale. By means of ultrafast lase
r pulses it became possible to monitor these events in real time with a tem
poral resolution in the sub-20 fs regime. Moving beyond the observation to
the control of chemical reactions requires additional theoretical and exper
imental effort. We illustrate with the aid of selected model systems the co
ncepts and possibilities of "passive" and "active" control and their differ
ences.