 Solution

First construct the energy cost for heterolysis from the molecular potential minimum. Dissociation to neutral atoms costs $D_e$, ionizing caesium costs $I$, and attachment of the electron to iodine releases EA. ThereforeFor the ground-state reference convention used above, the initial molecule already has vibrational zero-point energy. Thus its ground-state dissociation energy is $D_0=D_e-\frac{1}{2}{k}_B{\theta }_{\mathrm{vib}}$ andAt $3000\mathrm{K}$, $k_{B}T=0.258520\mathrm{eV}$, givingAlternatively, retaining the molecular minimum as reference gives $\Delta {\epsilon }_{\min }=4.36\mathrm{eV}$ and a Boltzmann factor $4.7372\times 10^{-8}$. That convention must use the full vibrational partition function, including $e^{-{\theta }_{\mathrm{vib}}/(2T)}$, in the next part. The ground-state convention instead uses $q_{\mathrm{vib}}^0$. Either consistent convention gives the same final equilibrium constant; using the ground-state reaction energy with the full zero-point factor would count the correction twice. The distinction between $D_e$ and $D_0$ is a distinction between initial states, not a change in the dissociation products.^[ref]