We propose a technique for ultrabroadband planar coherent Raman spectroscopy that enables wideband chemically selective mapping of molecular partition functions in the gas-phase within a single-laser-shot. A spectral region spanning 0–4200 cm−1 is excited simultaneously, in principle allowing for coherent planar imaging of most all fundamental Raman-active modes. This unique instantaneous and spatially correlated assessment enables multiplexed studies of transient dynamical systems in a two-dimensional (2D) field. Here, we demonstrate single-laser-shot high temperature diagnostics of H2, with spatially resolved 2D measurement of transitions of both the pure-rotational H2 S-branch and the vibrational H2 Q-branch, analyzing the temperature contour of a reacting fuel-species as it evolves at a flame-front.