The rate law(equation) relates
rate to
concentration of reacting species (such as substance A).
| Second order rate equation | |
| reaction rate = – | Δ[A] | = k[A]2 |
| Δt |
| First order rate equation | | |
| reaction rate = – | Δ[A] | = k[A] |
| Δt |
| Zero order rate equation | | |
| reaction rate = – | Δ[A] | = k |
| Δt |
The
relationship between
time and
concentration of substance A is also important because time is more easily measured than rate. This can be established by integrating each rate law. Integration is a mathematical process.
Integrated rate equations have a linear form (
y = mx + b) where, as shown below,
y is a function of [A] that depends on the order in A,
x is time,
m (the slope) is either +
k or –
k depending on the order and
b is a function of the initial concentration of A.
Zero order
integrated rate equation:[A] = –
kt + [A]
0 y = [A]
x =
tm = slope = -
k
First order
integrated rate equation:ln[A] = -
kt + ln[A]
0y = ln[A]
x =
tm = slope = -
k
Second order
integrated rate equation:y = 1/[A]
x =
tm = slope =
k
[A] against t is linear (constant slope), the reaction is zero order in A.
ln[A] against t is linear, the reaction is first order in A.
1/[A] against t is linear, the reaction is second order in A.
The rate constant k can be determined from the slopes of the lines.
Thus if a plot of