The Rate-Determining Step

This lesson covers: 

  1. What the rate-determining step is
  2. How the rate-determining step relates to the rate equation
  3. Predicting the rate equation from the rate-determining step
  4. Using the rate equation to deduce reaction mechanisms
  5. Intermediates in the rate-determining step

The slowest step determines the overall reaction rate

The rate-determining step (also known as the rate-limiting step) is the slowest step in a multi-step reaction mechanism. It dictates the overall rate of the reaction.


Just like how the flow of people exiting a crowded room is limited by how quickly they can get through the doorway, the rate of a multi-step reaction is restricted by its slowest step.


Each step in a reaction mechanism can have a different rate, but the step with the slowest rate controls how fast the reaction proceeds overall.

The rate equation reveals the rate-determining step

The rate equation provides valuable insights into the mechanism of a chemical reaction, particularly in identifying which reactants are involved in the rate-determining step.


Here are the key points to remember:

  • If a reactant appears in the rate equation, it must be involved in the rate-determining step, either directly or via a substance derived from it.
  • Conversely, if a reactant is absent from the rate equation, neither it nor any substance derived from it participates in the rate-determining step.


It's important to note that:

  1. The rate-determining step is not always the first step in the mechanism.
  2. The reaction mechanism usually cannot be deduced solely from the balanced equation.

Predicting the rate equation from the mechanism

The order of reaction with respect to a particular reactant indicates how many molecules of that reactant are involved in the rate-determining step.

For instance, if a reaction is second-order with respect to reactant X, then two molecules of X must be present in the rate-determining step.


Consider the following example.

The mechanism for the reaction between chlorine radicals and ozone (O3) consists of two steps:

Step 1 (slow):  Cl• + O3 ➔ ClO• + O2

Step 2 (fast):  ClO• + O3 ➔ Cl• + 2O2


To predict the rate equation, note that:

  • Both Cl• and O3 appear in the slow, rate-determining step, so both must be in the rate equation.
  • There is one Cl• radical and one O3 molecule in this step, so the reaction is first-order with respect to each.

Therefore, the rate equation takes the form: rate = k[Cl•][O3]

Using the rate equation to deduce the mechanism

Knowledge of which reactants feature in the rate-determining step can aid in deducing the reaction mechanism.


Let's examine an example.

The reaction below shows the substitution of Cl in chloromethane by the OH- nucleophile.

There are two potential mechanisms for this process.

Mechanism 1 (single-step)

A one-step process where the OH- nucleophile directly substitutes the Cl atom in a single transition state.

Diagram showing the substitution of Cl in chloromethane by the OH- nucleophile.

Mechanism 2 (two-step)

Step 1 (slow) - The C-Cl bond breaks, forming a carbocation intermediate and Cl-. This is likely the rate-determining step as breaking a strong C-Cl bond requires significant energy.


Step 2 (fast) - The positively charged carbocation rapidly reacts with the negatively charged OH- nucleophile to form the final product. If the OH- concentration is high, this step should occur quickly once the carbocation forms.

Diagram showing the substitution of Cl in chloromethane by OH- nucleophile with slow and fast steps.

The experimentally determined rate equation is:

rate = k[CH3Cl]

The absence of [OH-] in this equation indicates that OH- is not involved in the rate-determining step. This supports mechanism 2 being correct, where OH- only appears in the fast second step.

Intermediates in the rate-determining step

In some cases, the rate-determining step may involve an intermediate species that is formed and consumed during a reaction, but does not appear in the overall balanced equation.


Consider this example.

The reaction 2NO(g) + O2(g) ➔ 2NO2(g) proceeds via a two-step mechanism:

Step 1:  2NO ➔ N2O2

Step 2:  N2O2 + O2 ➔ 2NO2


If the rate equation is experimentally determined to be: rate = k[NO]2[O2], which step is rate-determining?


The rate equation tells us that the rate-determining step must involve:

  • 2 molecules of NO
  • 1 molecule of O2


Step 1 cannot be the rate-determining step as it does not involve O2. Although step 2 doesn't contain the reactants in the stoichiometry expected from the rate equation, it does involve the intermediate N2O2. This intermediate is derived from 2NO molecules, matching the rate equation.

Therefore, step 2 is the rate-determining step, even though it involves the intermediate N2O2 rather than the reactants shown in the overall equation.