Step 1: Recall the rate law for a first-order reaction.
For a first-order reaction, the rate is directly proportional to the concentration of one reactant. If we denote the reactant as A, the rate law is:
\[ \text{Rate} = k[A] \]
where:
$k$ is the rate constant.
$[A]$ is the concentration of the reactant.
Step 2: Understand the graph of Rate versus Concentration.
If we plot \text{Rate} on the y-axis and $[A]$ (concentration) on the x-axis for a first-order reaction, the equation is in the form of a straight line, $y = mx + c$, where $y = \text{Rate}$ and $x = [A]$.
In this case, the intercept $c$ is $0$, so the equation simplifies to $y = mx$.
Comparing \text{Rate} $= k[A]$ with $y = mx$, we can see that the slope ($m$) of the graph of \text{Rate} versus $[A]$ is equal to the rate constant ($k$).
\[ \text{Slope} = k \]
Step 3: Determine the value of the rate constant.
The problem states that the slope for the graph of rate versus concentration is $2.5 \times 10^{-3}$.
Since \text{Slope} $= k$, the rate constant $k$ is:
\[ k = 2.5 \times 10^{-3} \text{ time}^{-1} \]
The unit for a first-order rate constant is time$^{-1}$ (e.g., s$^{-1}$, min$^{-1}$).