Observation of different reactivities of para- and ortho-water towards cold diazenylium ions

Water, H$_2$O, is one of the fundamental molecules in chemistry, biology and astrophysics. It exists as two distinct nuclear-spin isomers, para- and ortho-water, which do not interconvert in isolated molecules. The experimental challenges in preparing pure samples of the two isomers have thus far precluded a characterization of their individual chemical behaviour. Capitalizing on recent advances in the electrostatic deflection of polar molecules, we separated the ground states of para- and ortho-water in a molecular beam to show that the two isomers exhibit different reactivities in a prototypical reaction with cold diazenylium ions (N$_2$H$^+$). Based on ab initio calculations and a modelling of the reaction kinetics using rotationally adiabatic capture theory, we rationalize this finding in terms of different rotational averaging of ion-dipole interactions during the reaction. The present results highlight the subtle interplay between nuclear-spin and rotational symmetry and its ramifications on chemical reactivity.