The influence of the photoabsorption process on the photodissociation
is investigated. To this end, the photodissociation of HCl as a model
system is studied, by integrating numerically the time dependent Schro
dinger equation for the simplified two-electronic-state problem, with
the time dependent coupling between the two states via the electromagn
etic radiation field included explicitly. The limits of the approximat
ion, which does not consider the absorption process explicitly, is dis
cussed. In this approximation the initial wave packet in the upper sta
te is obtained by projecting the vibrational function of the electroni
c ground state with the electronic transition dipole onto the upper el
ectronic state. Thus the absorption process is considered only implici
tly. It is demonstrated that the profile of the laser pulse and the he
ld strength of the light has a decisive influence on the dissociation
rates and the product distributions of the fragments. This cannot be d
escribed by using the approximation discussed.