Rate Equations (AQA A Level Chemistry): Revision Note
Exam code: 7405
Rate Equations
The rate of reaction refers to the change in the amount or concentration of a reactant OR product per unit time
It can be found by:
Measuring the decrease in the concentration of a reactant over time
Measuring the increase in the concentration of a product over time
The units for rate of reaction are mol dm-3 s-1
The rate of reaction is defined as the change in concentration of a reactant or product per unit time
It can be determined by:
Measuring the decrease in concentration of a reactant over time
Measuring the increase in concentration of a product over time
Mathematically, this can be expressed as:
rate = Δ[concentration] ÷ Δtime
When concentration is measured in mol dm⁻³ and time in seconds, the units of rate are mol dm⁻³ s⁻¹
Rate equation
The following general reaction will be used as an example to study the rate of reaction
D (aq) → Products
The rate of reaction at different concentrations of D is measured and tabulated
Rate of reactions table
3.00 | 2.00 x 10-3 | 6.67 x 10-4 |
2.00 | 1.33 x 10-3 | 6.67 x 10-4 |
1.00 | 6.60 x 10-4 | 6.67 x 10-4 |
A directly proportional relationship between the rate of the reaction and the concentration of D is observed when a graph is plotted
![Graph showing the relationship between rate and concentration [D], with gradient calculated as rate over [D], equalling 6.67 x 10⁻⁴.](https://cdn.savemyexams.com/cdn-cgi/image/f=auto,width=3840/https://cdn.savemyexams.com/uploads/2021/10/5.2.1-Rates-D-graph.png)
Rate equations must be determined experimentally
They cannot be deduced directly from the stoichiometric coefficients in the balanced equation
The general form of a rate equation is:
Rate = k[A]m[B]n
Where:
[A] and [B] are the concentrations of reactants
m and n are the orders of reaction with respect to each reactant
k is the rate constant
The orders (m and n) can be 0, 1, or 2, and they describe how the rate changes when the concentration of a reactant changes
Products are not included in the rate equation because the rate is determined by reactant concentrations in the forward reaction
For example:
In the reaction:
2NO(g) + 2H₂(g) → N₂(g) + 2H₂O(g)
The experimentally determined rate equation is:
Rate = k[NO]2[H2]
Notice that the order with respect to H2 is 1, not 2, even though the stoichiometric coefficient is 2
This shows that orders must be found experimentally
Interpreting the rate equation
If the concentration of NO is doubled (while [H2] remains constant), the rate increases by a factor of 4, showing second-order dependence on NO
If the concentration of H2 is doubled (while [NO] remains constant), the rate doubles, showing first-order dependence on H2
Catalysts and rate equations:
A catalyst will only appear in a rate equation if it is involved in the rate-determining step and its concentration affects the rate
This is usually the case for homogeneous catalysts (where the catalyst and reactants are in the same phase). If a species appears in the rate equation but not in the overall balanced equation, it is acting as a catalyst
Order of reaction
The order of a reactant describes how its concentration affects the rate of reaction
It is the power to which the concentration of that reactant is raised in the rate equation
The order with respect to a reactant can be 0, 1, or 2
If a reactant is zero order, changing its concentration does not affect the rate
In the rate equation, the concentration term is effectively absent because [A]o = 1
If a reactant is first order, the rate is directly proportional to its concentration
If a reactant is second order, the rate is proportional to the square of its concentration
The overall order of reaction is the sum of the powers of all reactant concentrations in the rate equation
For example, in the following rate equation,
Rate = k [NO]2 [H2]
The reaction is
Second-order with respect to NO
First-order with respect to H2
Third-order overall (2 + 1)
Examiner Tips and Tricks
You may come across the half-life in this topic. The half-life (t1/2) is the time taken for the concentration of a limiting reactant to become half of its initial value
The concept of a constant half-life proving a first-order reaction is scientifically correct, and you will be credited by examiners if you use it; however, it is not actually a required part of the AQA A-Level Chemistry syllabus.
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