For a first-order reaction R \(\rightarrow\) P, the integrated rate law is given by:
\( \ln[\text{R}]_t = -kt + \ln[\text{R}]_0 \).
Here:
- \([\text{R}]_t\) is the concentration of the reactant R at time t.
- \([\text{R}]_0\) is the initial concentration of the reactant R at time t=0.
- k is the first-order rate constant.
This equation is in the form of a straight line, \( y = mx + c \).
If we plot a graph with \(y = \ln[\text{R}]_t\) on the y-axis and \(x = t\) on the x-axis, we get:
\( \underbrace{\ln[\text{R}]_t}_{y} = \underbrace{(-k)}_{m} \underbrace{t}_{x} + \underbrace{\ln[\text{R}]_0}_{c} \).
From this comparison, we can see that:
- The slope of the line (m) is \(-k\). This matches the description of a straight line with a negative slope.
- The y-intercept (c), which is the value of y when x=0, is \( \ln[\text{R}]_0 \).
Therefore, the intercept on the y-axis is equal to \( \ln[\text{R}]_0 \).