Arrhenius Equation Calculator

Rate constant k, activation energy Ea from two temperatures, or k at a new temperature.

k = A·e^(−Ea/RT). From two measurements, Ea = R·ln(k₂/k₁) ÷ (1/T₁ − 1/T₂). If a rate constant goes from 0.0012 at 25 °C to 0.0048 at 45 °C, Ea = 8.314 × ln 4 ÷ (1/298.15 − 1/318.15) = 54.7 kJ/mol.

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How to use it

  1. Choose what to solve for: k, activation energy, or k at a new temperature.
  2. Enter the values you know; temperatures can be in °C or K.
  3. Read the result and, for two temperatures, how many times faster the reaction runs.

What you enter

What you get

Formula

k = A·e^(−Ea/RT) | ln(k₂/k₁) = (Ea/R)(1/T₁ − 1/T₂)

R = 8.314 J/(mol·K); T in kelvin (°C + 273.15); Ea in J/mol inside the exponent.

Worked example: activation energy

Input: k₁ = 0.0012 at 25 °C, k₂ = 0.0048 at 45 °C

Result: Ea = 54.7 kJ/mol

Typical of many enzyme-free solution reactions; a 20 °C rise quadruples the rate.

Questions

What does the Arrhenius equation tell you?

How a reaction's rate constant depends on temperature. A higher activation energy means the rate is more sensitive to temperature.

How do I find activation energy from two temperatures?

Use Ea = R × ln(k₂/k₁) ÷ (1/T₁ − 1/T₂) with temperatures in kelvin and R = 8.314 J/(mol·K). Divide by 1000 for kJ/mol.

Does a 10 °C rise really double the rate?

Only for activation energies of roughly 50 kJ/mol near room temperature. The rule of thumb is the Q10 idea; the Arrhenius equation gives the exact factor for your Ea.

What are the units of A?

The same as k, so they depend on the reaction order: s⁻¹ for first order, M⁻¹·s⁻¹ for second order.

Limitations

References

More Chemistry

All free tools · By Dr. Zubair Khalid, DVM, MS, PhD.