The process consists of three steps forming a cycle. The total heat exchanged in a cyclic process is equal to the total work done by the system, since the change in internal energy for a cyclic process is zero (\( \Delta U_{cyclic} = 0 \)).
The total heat \( Q_T = \omega_1 + \omega_2 + \omega_3 \), where \( \omega_1, \omega_2, \omega_3 \) are the work done in the isothermal expansion, isobaric compression, and isochoric heating, respectively.
Step 1: Isothermal expansion from \( (P_0, V_0) \) to \( (P_1, 4V_0) \).
For an isothermal process, \( PV = constant \),
so \( P_0 V_0 = P_1 (4V_0) \Rightarrow P_1 = \frac{P_0}{4} \).
Work done \( \omega_1 = \int_{V_0}^{4V_0} P dV = \int_{V_0}^{4V_0} \frac{P_0 V_0}{V} dV = P_0 V_0 [\ln V]_{V_0}^{4V_0} = P_0 V_0 (\ln(4V_0) - \ln V_0) = P_0 V_0 \ln \frac{4V_0}{V_0} = P_0 V_0 \ln 4 = P_0 V_0 (2 \ln 2) \).
Step 2: Isobaric compression from \( (\frac{P_0}{4}, 4V_0) \) to \( (\frac{P_0}{4}, V_0) \).
Work done \( \omega_2 = \int_{4V_0}^{V_0} P dV = P_1 (V_0 - 4V_0) = \frac{P_0}{4} (-3V_0) = -\frac{3}{4} P_0 V_0 = -0.75 P_0 V_0 \).
Step 3: Isochoric heating from \( (\frac{P_0}{4}, V_0) \) to \( (P_0, V_0) \).
For an isochoric process, the volume is constant (\( dV = 0 \)). Work done \( \omega_3 = \int_{V_0}^{V_0} P dV = 0 \).
The total heat exchanged in the process is the sum of the work done in each step: \[ Q_T = \omega_1 + \omega_2 + \omega_3 = 2 P_0 V_0 \ln 2 - 0.75 P_0 V_0 + 0 = P_0 V_0 (2 \ln 2 - 0.75) \]
To solve this problem, we follow the steps of the thermodynamic process described: isothermal expansion, isobaric compression, and isochoric heating.
To find the total heat exchanged, \(Q_{\text{total}}\), sum the heat exchanged in each process:
\(Q_{\text{total}} = Q_1 + Q_2 + Q_3 = P_0 V_0 \cdot 2 \ln 2 - 3P_0 V_0 + 2.25P_0 V_0\)
Simplifying, we obtain:
\(Q_{\text{total}} = P_0 V_0 (2 \ln 2 - 0.75)\)
Thus, the correct option is: \( P_0 V_0 (2 \ln 2 - 0.75) \). This matches with the option given in the question, confirming the step-by-step calculations.
For a given reaction \( R \rightarrow P \), \( t_{1/2} \) is related to \([A_0]\) as given in the table. Given: \( \log 2 = 0.30 \). Which of the following is true?
| \([A]\) (mol/L) | \(t_{1/2}\) (min) |
|---|---|
| 0.100 | 200 |
| 0.025 | 100 |
A. The order of the reaction is \( \frac{1}{2} \).
B. If \( [A_0] \) is 1 M, then \( t_{1/2} \) is \( 200/\sqrt{10} \) min.
C. The order of the reaction changes to 1 if the concentration of reactant changes from 0.100 M to 0.500 M.
D. \( t_{1/2} \) is 800 min for \( [A_0] = 1.6 \) M.
