For first-order reactions, remember that the slope of the log(concentration) vs. time plot is always \(\frac{-k}{2.303}\).
For a first-order reaction, the integrated rate law is:
\( \ln[A] = -kt + \ln[A]_0 \)
where [A] is the concentration at time t, k is the rate constant, and \([A]_0\) is the initial concentration. Taking the logarithm to base 10:
\( \log[A] = \frac{-k}{2.303}t + \log[A]_0 \)
This equation is of the form \(y = mx + c\), where:
- \(y = \log[A]\),
- \(x = t\),
- \(m = \frac{-k}{2.303}\),
- \(c = \log[A]_0\).
Thus, the slope of the plot of log(reactant concentration) against time is \(\frac{-k}{2.303}\).
The rate of a reaction:
A + B −→ product
is given below as a function of different initial concentrations of A and B.
Experiment | \([A]\) (mol L\(^{-1}\)) | \([B]\) (mol L\(^{-1}\)) | Initial Rate (mol L\(^{-1}\) min\(^{-1}\)) |
---|---|---|---|
1 | 0.01 | 0.01 | \(5 \times 10^{-3}\) |
2 | 0.02 | 0.01 | \(1 \times 10^{-2}\) |
3 | 0.01 | 0.02 | \(5 \times 10^{-3}\) |