Differences in pKa and related thermodynamic acidity parameters consistently govern chemical reactivity and reaction kinetics across various molecular systems.
The retrieved literature consistently supports the chemical principle that changes in acidity, proton-coupled thermodynamics, and related structural parameters directly dictate reaction rates and chemical reactivity trends. Papers [0], [1], [2], and [6] explicitly demonstrate the quantitative relationships between acid-base/thermodynamic properties and kinetic or reactivity outcomes. No papers refute this principle.