AQA A-Level Chemistry 7405 · 3.1.9 Rate equations

Part 1: Orders, initial rates and the rate constant

All 3 parts available · worked answers and exam guidance included. Reviewed 2 October 2026.

Use experimental evidence to build a rate equation, predict rate changes and derive the correct units of k.

A rate equation is an experimental model

In rate = k[A]ᵐ[B]ⁿ, square brackets mean concentration in mol dm⁻³, m and n are the orders with respect to A and B, and k is the rate constant at the stated temperature. The overall order is m + n. The order is the power to which a concentration is raised in the experimentally determined rate equation. AQA uses individual orders 0, 1 and 2 in this section.

The overall balanced equation tells you stoichiometry, not the experimental orders. A catalyst can appear in a rate law even though it cancels from the overall equation. A zero-order reactant can still be essential to the reaction; its concentration does not affect the measured rate over the range investigated.

For fixed conditions and reaction pathway, k does not fall merely because reactants are being used up. Their changing concentrations change the rate. A change of temperature or catalyst can change k.

rate = k[A]ᵐ[B]ⁿ
rate₂/rate₁ = ([A]₂/[A]₁)ᵐ × ([B]₂/[B]₁)ⁿ

Isolate the effect of each reactant

Compare experiments in which only one concentration changes. State the concentration factor and the rate factor, then identify the power connecting them. With noisy data, use the trend and experimental precision rather than demanding exact integer ratios.

Changing just one concentration at constant temperature
OrderDoubling concentrationRate against concentration
ZeroRate unchanged.Horizontal line within the measured range.
FirstRate doubles.Straight line through origin.
SecondRate quadruples.Upward curve; rate against concentration squared is straight.

Worked initial-rate table

These are original illustrative data at one fixed temperature. All concentrations are initial concentrations after mixing.

Rate experiment
Run[A] / mol dm⁻³[B] / mol dm⁻³Rate / mol dm⁻³ s⁻¹
10.1200.2002.40 × 10⁻⁴
20.2400.2004.80 × 10⁻⁴
30.2400.4001.92 × 10⁻³

When two concentrations change together

If A is known to be first order, doubling A accounts for a factor of two in rate. If B also triples and the total rate rises by eighteen, B accounts for 18/2 = 9; therefore B is second order because 3² = 9. Do not assign the whole rate change to B.

A log(rate)-versus-log(concentration) plot has gradient equal to the order when all other relevant concentrations and conditions are fixed. Use the same logarithm base on both axes. This is a useful way to test a wider dataset.

Derive units rather than guessing

Rearrange k = rate/(concentration terms), insert units, then cancel powers. The rate unit must match the measurement: if time is in minutes, the time factor in k is min⁻¹. Standard concentration-rate calculations here use seconds.

Using rate in mol dm⁻³ s⁻¹
Overall orderUnits of k
0mol dm⁻³ s⁻¹
1s⁻¹
2dm³ mol⁻¹ s⁻¹
3dm⁶ mol⁻² s⁻¹

Quick checks

Original Finesse questions. Reveal the indicative worked solutions after attempting each question; these are not official AQA mark allocations.

Q1. Tripling A multiplies the rate by nine at fixed B. What is the order in A?Show answer

Second order: 3² = 9.

Q2. For rate = k[A]²[B], what happens if A halves and B doubles?Show answer

The factor is (½)² × 2 = ½. The rate halves.

Q3. Rate = 3.60 × 10⁻⁴ mol dm⁻³ s⁻¹ at [A] = 0.0300 mol dm⁻³ for rate = k[A]². Find k.Show answer

k = (3.60 × 10⁻⁴)/(0.0300²) = 0.400 dm³ mol⁻¹ s⁻¹.

Q4. A and B both double and the rate increases eightfold. A is first order. Find B’s order.Show answer

A contributes ×2. B contributes ×4, so B is second order.

Q5. Can an overall coefficient of two prove second order?Show answer

No. The rate law must be determined experimentally unless an elementary-step model is explicitly supplied and applicable.

Sources

Sources and examiner guidance (reviewed 2 October 2026)

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