Step 1: Start with the integrated rate law for a first-order reaction.
The integrated rate law relates the initial concentration of a reactant, [A]\(_0\), to its concentration at any time t, [A]\(_t\), for a rate constant k.
\[
\ln\frac{[\text{A}]_0}{[\text{A}]_t} = kt
\]
Alternatively, in base-10 logarithm form:
\[
k = \frac{03}{t} \log_{10}\frac{[\text{A}]_0}{[\text{A}]_t}
\]
Step 2: Define half-life (\(t_{1/2}\)).
Half-life is the time required for the concentration of a reactant to decrease to half of its initial value.
At \( t = t_{1/2} \), the concentration \( [\text{A}]_t = \frac{1}{2}[\text{A}]_0 \).
Step 3: Substitute the half-life condition into the integrated rate law.
Using the natural logarithm form:
\[
\ln\frac{[\text{A}]_0}{\frac{1}{2}[\text{A}]_0} = k \cdot t_{1/2}
\]
Step 4: Simplify the equation.
The [A]\(_0\) terms cancel out:
\[
\ln(2) = k \cdot t_{1/2}
\]
Step 5: Solve for half-life (\(t_{1/2}\)).
Since \(\ln(2) \approx 0.693\):
\[
0.693 = k \cdot t_{1/2}
\]
\[
t_{1/2} = \frac{0.693}{k}
\]
This is the relation between the half-life and the rate constant for a first-order reaction. It shows that the half-life is constant and independent of the initial concentration of the reactant.