To solve the problem, let's consider the details of the reaction given:
The reaction is zero-order, denoted as \( A \to \text{product} \), where the rate is independent of the concentration of the reactant.
The formula for the half-life of a zero-order reaction is:
\(t_{1/2} = \frac{[A]_0}{2k}\)
where \([A]_0\) is the initial concentration and \(k\) is the rate constant.
Given that the half-life (\( t_{1/2} \)) is 1 hour and \([A]_0 = 2.0 \, \text{mol L}^{-1}\), we can calculate \(k\):
\(1 = \frac{2.0}{2k}\)
Solving for \( k \):
\(k = 1.0 \, \text{mol L}^{-1} \text{h}^{-1}\)
Next, we want to find the time required to decrease the concentration of \(A\) from 0.50 mol L-1 to 0.25 mol L-1. For a zero-order reaction, the time (\( t \)) for the concentration change from \([A]_0\) to \([A]\) is given by:
\(t = \frac{[A]_0 - [A]}{k}\)
Substituting the given values:
\(t = \frac{0.50 - 0.25}{1.0} = 0.25 \, \text{hours}\)
Since we need to find the time in minutes:
\(0.25 \, \text{hours} \times 60 \, \text{min/hour} = 15 \, \text{minutes}\)
Therefore, the time required to decrease the concentration of A from 0.50 mol L-1 to 0.25 mol L-1 is 15 minutes.
Hence, the correct answer is: 15 min.
For the reaction \( A + B \to C \), the rate law is found to be \( \text{rate} = k[A]^2[B] \). If the concentration of \( A \) is doubled and \( B \) is halved, by what factor does the rate change?


In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: