Thermodynamics is often perceived as a labyrinth of equations, but at its core, it is a beautiful story of energy transformation. In this problem, we are presented with a classic scenario: one mole of a monatomic ideal gas undergoing a cyclic process. The journey is mapped out on a Pressure-Temperature (P-T) diagram, forming a neat rectangle through states J→K→L→M→J. Our mission is to dissect this cycle, analyze each leg, and match the thermodynamic quantities to their correct values.
Decoding the P-T Diagram
Before diving into calculations, let's orient ourselves. A P-T diagram is incredibly revealing. A horizontal line indicates a process where pressure is constant—an isobaric process. A vertical line indicates a process where temperature is constant—an isothermal process.
Our cycle consists of two isobaric processes (J→K and L→M) and two isothermal processes (K→L and M→J). Since the gas is monatomic, we know its molar heat capacity at constant volume is CV=23R.
Analyzing Process J→K
Isobaric Expansion
Let's begin with the first leg, from state J to state K. The graph shows a horizontal line at a constant pressure P0. The temperature, however, increases from T0 to 3T0.
We are asked to find the change in internal energy (ΔUJK). For any ideal gas, the change in internal energy depends solely on the change in temperature, governed by the equation:
Substituting our known values (n=1, CV=23R, and ΔT=3T0−T0=2T0), we get:
ΔUJK=(1)(23R)(2T0)=3RT0
This perfectly matches option (3) in List-II. So, (Q) maps to (3).
Analyzing Process K→L
Isothermal Compression
Next, the gas moves from K to L. Here, the temperature is locked at 3T0, making it an isothermal process. The pressure increases from P0 to 2P0.
We need to find the heat given to the gas (QKL). The First Law of Thermodynamics states that Q=ΔU+W. Since the process is isothermal, the temperature doesn't change, meaning ΔUKL=0. Therefore, the heat exchanged is exactly equal to the work done: QKL=WKL.
For an isothermal process, the work done can be expressed in terms of pressure as:
Plugging in the values for this specific leg (T=3T0, Pi=P0, Pf=2P0):
QKL=(1)R(3T0)ln(2P0P0)=−3RT0ln2
This matches option (5). Thus, (R) maps to (5).
Analyzing Process M→J
Isothermal Expansion
Let's skip ahead to the final leg, M→J, to find its change in internal energy. Just like K→L, this is a vertical line on the P-T diagram, meaning the temperature is constant at T0.
As we established earlier, if there is no change in temperature (ΔT=0), there is absolutely no change in the internal energy of an ideal gas.
This straightforward deduction matches option (2). Therefore, (S) maps to (2).
The Grand Finale
Total Work Done
Finally, we must calculate the total work done in the complete cyclic process. This is the algebraic sum of the work done in all four individual legs:
Wtotal=WJK+WKL+WLM+WMJ
We already know WKL=−3RT0ln2. Let's find the work for the remaining three processes.
For the isobaric processes (J→K and L→M), the work done is simply W=nRΔT:
WJK=R(3T0−T0)=2RT0
WLM=R(T0−3T0)=−2RT0
Notice the beautiful symmetry! The work done during the isobaric expansion is perfectly canceled out by the work done during the isobaric compression. WJK+WLM=0.
Now, let's calculate the work for the final isothermal process, M→J:
WMJ=nRTMln(PJPM)=R(T0)ln(P02P0)=RT0ln2
Adding the non-zero components together yields the total work:
Wtotal=WKL+WMJ=−3RT0ln2+RT0ln2=−2RT0ln2
This matches option (4). So, (P) maps to (4).
By systematically breaking down the cycle and applying fundamental thermodynamic principles, we have successfully decoded the entire problem. The final mapping is P → 4, Q → 3, R → 5, S → 2.