Polanyi 1 clearly predicted the possibility of stimulated emission from HC1 due to selective vibrational excitation in the chemical reaction H + Cl 2 -HClt + CI. We have recorded such emission and laser oscillation in a few P-branch transitions of HC1 formed in reactions initiated by flash photodissociation of chlorine in a Cl 2 -H 2 mixture. We believe this is the first operating laser based upon excitation by a chemical reaction. Vibrational-rotational laser transitions have been observed earlier by Patel, Faust, and McFarlane 2 but by other means of excitation: C0 2 2 and CO 3 in electric discharges, andC0 2 4 and N z O 5 through transfer of vibrational energy from N 2 t.Emission was studied either from a Ramantype multiple-reflection cell 8 containing a flash photolysis tube, or from a 60-em, 14-mm i.d. quartz laser tube fitted with normally polished sodium chloride discs affixed at the Brewster angle. A third disc, tilted at a 10° angle, deflected 8.2% of the light out of the confocal cavity formed by two gold-surfaced mirrors (radius, 1 m) placed 86.5 cm apart. The emission from the multiple-reflection cell was studied with the rapid-scan spectrometer, sometimes 10 20 30 TIME (>iSEC)FIG.