A-Level Chemistry AQA 7405

1.9: Rate equations

#1.9.1

Rate equations

The rate of a chemical reaction is related to the concentration of reactants by a rate equation of the form:

Rate = kAm Bn

where m and n are the orders of reaction with respect to reactants A and B and k is the rate constant.

The orders m and n are restricted to the values 0, 1, and 2.

The rate constant k varies with temperature as shown by the Arrhenius equation: k=AeEaRTk = Ae^{-\dfrac{E_a}{RT}} where A is a constant, known as the Arrhenius constant, Ea is the activation energy and T is the temperature in K.

Students should be able to:

  • define the terms order of reaction and rate constant
  • perform calculations using the rate equation
  • explain the qualitative effect of changes in temperature on the rate constant k
  • perform calculations using the Arrhenius equation
  • understand that the Arrhenius equation can be rearranged into the form lnk=EaRT+lnA\ln{k} = -\dfrac{E_a}{RT} + \ln{A} and know how to use this rearranged equation with experimental data to plot a straight line graph with slope EaR-\dfrac{E_a}{R}

These equations and the gas constant, R, will be given when required.

#1.9.2

Determination of rate equation

The rate equation is an experimentally determined relationship.

The orders with respect to reactants can provide information about the mechanism of a reaction.

Students should be able to:

  • use concentration–time graphs to deduce the rate of a reaction
  • use initial concentration–time data to deduce the initial rate of a reaction
  • use rate–concentration data or graphs to deduce the order (0, 1 or 2) with respect to a reactant
  • derive the rate equation for a reaction from the orders with respect to each of the reactants
  • use the orders with respect to reactants to provide information about the rate determining/limiting step of a reaction.
#1.9P7

Required practical 7

Measuring the rate of reaction:

  • by an initial rate method
  • by a continuous monitoring method.
1.8
Thermodynamics
1.10
Equilibrium constant Kp for homogeneous systems