It increases by a factor of 4.
It doubles.
The rate law is given by:
\[ \text{Rate} = k[A]^2[B] \]
Let's say the initial concentrations of \( A \) and \( B \) are \( [A]_0 \) and \( [B]_0 \), and the initial rate is: \[ \text{Rate}_0 = k[A]_0^2[B]_0 \]
The concentration of \( A \) is doubled: \[ [A]_{\text{new}} = 2[A]_0 \] The concentration of \( B \) is halved: \[ [B]_{\text{new}} = \frac{1}{2}[B]_0 \]
Substituting the new concentrations into the rate law: \[ \text{Rate}_{\text{new}} = k(2[A]_0)^2\left(\frac{1}{2}[B]_0\right) \] \[ \text{Rate}_{\text{new}} = k \cdot 4[A]_0^2 \cdot \frac{1}{2}[B]_0 \] Simplifying: \[ \text{Rate}_{\text{new}} = 2k[A]_0^2[B]_0 \]
The initial rate was: \[ \text{Rate}_0 = k[A]_0^2[B]_0 \] The new rate is: \[ \text{Rate}_{\text{new}} = 2 \cdot \text{Rate}_0 \]
The rate of the reaction doubles, so the correct answer is \( \boxed{\text{It doubles.}} \).
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.