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Integrated rate laws: concentration over time and half-life

Find the concentration of a reactant after a given time, the half-life and the time to reach a target concentration for zero-, first- and second-order reactions.

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Reaction order

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mol/L

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mol/L

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Results

Concentration after the time elapsed, [A]

0.3679 mol/L

Share of the reactant remaining
36.8%
Half-life (from [A]₀)
69.31
First order: the half-life does not depend on concentration
Time to reach the target concentration
230.3
Rate at the time elapsed, k[A]ⁿ
0.003679 mol/(L·time)

How fast does a reactant disappear?

The rate of a chemical reaction usually depends on the concentration of its reactants. A rate law such as rate = k[A]ⁿ links the two, where k is the rate constant and n the order of the reaction. Integrating that equation over time gives the integrated rate law, which tells you how much reactant is left after any time, how long it takes to reach a given concentration and what the half-life is.

The three common orders

Order Integrated law Half-life Straight-line plot
0 [A] = [A]₀ − kt [A]₀ ÷ 2k [A] against t
1 [A] = [A]₀ × e^(−kt) ln 2 ÷ k ln[A] against t
2 1/[A] = 1/[A]₀ + kt 1 ÷ (k[A]₀) 1/[A] against t

The time to reach a target concentration comes from solving each law for t, for example t = ln([A]₀ ÷ [A]) ÷ k at first order.

Example

A first-order reaction with k = 0.01 s⁻¹ and an initial concentration of 1 mol/L:

  • After 100 s: [A] = e^(−1) = 0.3679 mol/L, so 36.8% remains
  • Half-life: 0.6931 ÷ 0.01 = 69.31 s
  • Time to fall to 0.1 mol/L: ln 10 ÷ 0.01 = 230.3 s
  • Rate at 100 s: 0.01 × 0.3679 = 0.00368 mol/(L·s)

Where each order appears

  • Zero order: reactions limited by a saturated catalyst or enzyme, such as alcohol elimination by the liver at high blood levels, and some surface reactions.
  • First order: radioactive decay, many decompositions such as N₂O₅, and the elimination of most drugs.
  • Second order: reactions where two molecules of the same species collide, such as the dimerization of NO₂ or of butadiene.

Half-lives that change

At first order, every half-life is the same. At zero order, each successive half-life is half as long as the one before, because the reactant is consumed at a constant rate. At second order, each one is twice as long, because the rate falls quickly as the reactant runs out.

Temperature

The rate constant k depends strongly on temperature, often doubling for every 10 °C rise near room temperature. The Arrhenius equation, k = A × e^(−Ea/RT), describes that dependence and lets you convert k from one temperature to another before using this calculator.

Frequently asked questions

What is an integrated rate law?

An equation that gives the concentration of a reactant as a function of time, obtained by integrating the rate law. Its form depends on the reaction order: linear for zero order, exponential for first order and hyperbolic for second order.

How do I find the order of a reaction?

Plot the data three ways: [A] against time is a straight line for zero order, ln[A] against time for first order and 1/[A] against time for second order. The slope of the straight line gives k.

Why is first-order half-life constant?

For a first-order reaction, t½ = ln 2 ÷ k, which does not depend on concentration. Each half-life removes half of what is left, which is why radioactive decay and many drug eliminations are described by half-lives.

What units does k have?

For zero order, mol/(L·s); for first order, 1/s; for second order, L/(mol·s), with any time unit you like. Use the same time unit for k and for the time entered.

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Results are estimates provided for information purposes. They do not replace professional advice.