Step 1 — Recall the half-life formula for a first-order reaction
For a first-order reaction the half-life is independent of concentration and is given by the well-known formula:
\( \displaystyle t_{1/2} = \frac{\ln 2}{k} \).
Step 2 — Substitute values and compute
Use \(\ln 2 \approx 0.693147\) (often approximated as 0.693).
\[
t_{1/2} = \frac{0.693147\ldots}{0.0693\ \text{min}^{-1}}
\approx \frac{0.693147}{0.0693}.
\]
Since \(0.0693\times 10 = 0.693\), the quotient is approximately
\[
t_{1/2} \approx 10.00\ \text{min}.
\]
(Using the more precise ln2 gives \(t_{1/2}\approx 0.693147/0.0693 \approx 10.002\) min, which rounds to 10.0 min.)
Step 3 — Units and significant figures
• The rate constant k is given in min⁻¹, so the resulting time is in minutes.
• Given k = 0.0693 (4 significant digits) and ln2 ≈ 0.6931, the half-life computed to two or three significant figures is 10.0 min. For typical multiple-choice reporting, 10 min is the correct choice.
Quick verification
If \(t_{1/2}=10\) min, then \(k = \ln2 / t_{1/2} \approx 0.693147/10 = 0.0693147\ \text{min}^{-1}\), which matches the given k = 0.0693 min⁻¹ within the given precision.
Final answer (clear)
The half-life is \( \boxed{\,10\ \text{min}\,} \). (Select the option: 10 min.)
Note: This derivation follows directly from the integrated first-order rate law. The result is independent of initial concentration and depends only on k.
For a first order decomposition of a certain reaction, rate constant is given by the equation
\(\log k(s⁻¹) = 7.14 - \frac{1 \times 10^4 K}{T}\). The activation energy of the reaction (in kJ mol⁻¹) is (\(R = 8.3 J K⁻¹ mol⁻¹\))
Note: The provided value for R is 8.3. We will use the more precise value R=8.314 J K⁻¹ mol⁻¹ for accuracy, as is standard.