To determine the first-order rate constant for reaction I, we need to use the information given about both reactions.
The reactions are:
The rate of disappearance of Br^− in reaction II is given as -\frac{d[Br^-]}{dt} = 2 \times 10^{-4} \text{ mol L}^{-1} \text{min}^{-1}.
The stoichiometry of reaction II shows that for every 5 moles of Br^{-} consumed, 1 mole of BrO_3^{-} reacts. Therefore, the rate of the entire balanced reaction can be based on the stoichiometry and the rate of change of Br^−:
Rate of reaction II = \frac{-1}{5}\frac{d[Br^-]}{dt}
\frac{-1}{5}(2 \times 10^{-4}) = 4 \times 10^{-5} \text{ mol L}^{-1} \text{min}^{-1}
Given that the rates of both reactions are the same at 10.10 am:
Rate_{\text{reaction I}} = Rate_{\text{reaction II}}
k[A] = 4 \times 10^{-5}
where k is the rate constant for reaction I and [A] = 10^{-2} \text{ mol L}^{-1} at 10.10 am.
Therefore, solve for k:
k \cdot 10^{-2} = 4 \times 10^{-5}
k = \frac{4 \times 10^{-5}}{10^{-2}} = 4 \times 10^{-3} \text{ min}^{-1}
Thus, the first-order rate constant for reaction I is 4 \times 10^{-3} \text{ min}^{-1}.