Pump-probe spectra of HeBr 2 in vibrational states vЈϭ10 and 39 through 48 of the B electronic state are reported and the fragment rotational distributions from vibrational predissociation of the cluster are extracted from the measured E(0 g ϩ )←B( 3 ⌸ 0u ϩ ) spectra of Br 2 . The experimental results are compared to theoretical calculations on the B←X spectra using atom-atom model potentials and performing a thermal average over transitions that contribute to the net excitation. Very good agreement between experiment and theory is obtained, except in the region of vЈϭ44, where the ⌬vϭϪ1 channel closes, and in the region of vЈϭ48 where the ⌬vϭϪ2 channel closes. For vЈ ϭ43, and vЈϭ44, the agreement is less satisfactory because the dynamics are extremely sensitive to details of the potential energy surface due to threshold effects associated with the ⌬vϭϪ1 channel closing. Similar sensitivity to the potential due to the ⌬vϭϪ2 channel closing impairs the agreement between experiment and theory for vЈϭ48. Below vЈϭ43, the rotational distributions for ⌬vϭϪ1 and ⌬vϭϪ2 are quite similar. Above vЈϭ43 the peaks of the rotational distributions for ⌬vϭϪ2 move to higher values of j. These results are compatible with the theoretical conclusion that dissociation shifts from a direct mechanism to one involving intramolecular vibrational distribution in the region of the closing of the ⌬vϭϪ1 channel. Although the simple additive potential model used in this work succeeds in reproducing most of the experimental data for this system, further improvements in the potential energy surface will be required to achieve precise agreement between experiment and theory for large Br-Br separations.