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.
The rate of a reaction:
A + B −→ product
is given below as a function of different initial concentrations of A and B.
Experiment | \([A]\) (mol L\(^{-1}\)) | \([B]\) (mol L\(^{-1}\)) | Initial Rate (mol L\(^{-1}\) min\(^{-1}\)) |
---|---|---|---|
1 | 0.01 | 0.01 | \(5 \times 10^{-3}\) |
2 | 0.02 | 0.01 | \(1 \times 10^{-2}\) |
3 | 0.01 | 0.02 | \(5 \times 10^{-3}\) |
The percentage error in the measurement of mass and velocity are 3% and 4% respectively. The percentage error in the measurement of kinetic energy is: