Reaction dynamics
Start with the big picture
A reaction’s rate law describes how its rate responds to reactant concentrations, while its overall order is determined experimentally and need not match the reaction’s stoichiometry. For an elementary step, molecularity provides the basis for its rate law. In a multistep mechanism, the slow rate-determining step helps govern the observed kinetics; steady-state and pre-equilibrium approximations can simplify expressions involving intermediates. Collision theory and the Arrhenius equation relate reaction rates to molecular encounters and temperature, while transition state theory and reaction-coordinate diagrams describe barriers and activated complexes. The broader topic also considers isotope effects, pressure-dependent unimolecular reactions, chain and photochemical reactions, diffusion control, and additional kinetic models.
What you'll learn
- Distinguish empirical reaction order from stoichiometric coefficients and elementary-step molecularity.
- Explain how a rate-determining step relates a mechanism to observed kinetics.
- Describe when steady-state and pre-equilibrium approximations simplify rate expressions.
- Relate collision theory, the Arrhenius equation, and transition state theory to reaction rates.
- Recognize how reaction diagrams and selected kinetic effects inform mechanism analysis.
Continue your study
Work through the complete notes and reinforce the topic with the study tools available in the full lesson.