Step 1: For isothermal processes, the change in internal energy of an ideal gas is zero. The first law of thermodynamics gives the relationship \( q = -w \). The work done during an isothermal irreversible process can be calculated as \( P_{\text{ext}} (V_{\text{final}} - V_{\text{initial}}) \), which matches Statement-I. Therefore, Statement-I is correct.
Step 2: For an adiabatic process, there is no heat exchange (\( q = 0 \)), and the change in internal energy is equal to the work done, \( \Delta U = W_{\text{adiabatic}} \), which matches Statement-II. Therefore, Statement-II is also correct. Thus, both Statement-I and Statement-II are correct.

Reactant ‘A’ underwent a decomposition reaction. The concentration of ‘A’ was measured periodically and recorded in the table given below:
Based on the above data, predict the order of the reaction and write the expression for the rate law.
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.