Using the model
Symbols, assumptions and limitations
Reaction orders are empirical and are not generally equal to balanced-equation coefficients. Concentrations must be in mol/L and time must use one consistent unit. Integrated forms assume a single reactant, constant temperature, constant volume, and one unchanging rate law.
Worked examples
See the method in practice
Two-reactant rate law
For r = k[A]²[B], doubling A multiplies rate by four, while doubling B multiplies it by two; the overall order is three.
First-order decay
For a first-order process, [A]t = [A]0e⁻ᵏᵗ and the half-life is ln 2/k, independent of initial concentration.
Questions
Frequently asked
Can reaction order be read from the balanced equation?
Usually not. Orders must be determined experimentally, except for an established elementary step.
Why do the units of k change?
The rate always has concentration-per-time units, so the dimensions of k compensate for the overall reaction order.
Does a catalyst change the equilibrium constant?
No. A catalyst changes forward and reverse rates, helping equilibrium to be reached faster without changing its position.
Sources & review
Equations and examples are checked against the references below. Results are educational and should be independently verified for safety-critical work.
OpenStax Chemistry — Factors Affecting Reaction Rates OpenStax Chemistry — Integrated Rate LawsWritten by the STEM Hub editorial team · Reviewed August 11, 2026 · Review methodology