How to use (3 steps)
- Choose a mode: integrated rate law, data fitting, or Arrhenius.
- Enter A₀, k and t for theory, paste measured (t, [A]) or (T, k) data for fitting.
- Read off [A](t), fraction remaining, t₁/₂, best-fit order and Arrhenius parameters, then copy the URL to share the setup.
A default 1st-order example and small datasets are preloaded so you can see results and plots immediately.
Results
Mode: Integrated rate law
This section summarizes the main quantities computed from your inputs (concentration, fraction remaining, half-life, fitted constants and Arrhenius parameters).
How it is calculated
- Steps will appear here after calculation.
FAQ
Which reaction orders does this tool support?
It focuses on simple 0th, 1st and 2nd order kinetics for a single reactant A, using the integrated forms [A](t) = [A]₀ − k t, ln[A] = ln[A]₀ − k t and 1/[A] = 1/[A]₀ + k t. For more complex mechanisms or mixed orders, treat this calculator as a first diagnostic rather than a full kinetic model.
How should I format data for the fitting and Arrhenius modes?
For data fitting, paste time and concentration pairs as t, A on separate lines (all A values must be positive). For Arrhenius plots, paste T, k pairs with T in kelvins and k > 0. The calculator performs straight-line fits to the transformed data and reports slopes, intercepts, R² and kinetic parameters.
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