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Question: For 1 mole of an ideal monatomic gas on moving from one state to another, the temperature is doubled...

For 1 mole of an ideal monatomic gas on moving from one state to another, the temperature is doubled but pressure becomes 2\sqrt {\text{2}} times. The entropy change in the process will be (R=2 cal/molK)\left( {R = 2{\text{ cal/mol}} \cdot {\text{K}}} \right)
(A) R ln2R{\text{ ln2}}
(B) 2R ln2{\text{2}}R{\text{ ln2}}
(C) 3R ln2{\text{3}}R{\text{ ln2}}
(D) R2 ln2\dfrac{R}{2}{\text{ ln2}}

Explanation

Solution

The measure of randomness or disordered distribution is known as entropy. The randomness is always higher in a gaseous state. More the number of gaseous molecules higher is the entropy.

Complete step by step solution:
First we will derive an equation for entropy in terms of temperature and pressure.
The equation for the change in entropy is as follows:
ΔS=ΔQT\Delta S = \dfrac{{\Delta Q}}{T} ………..…… (1)
Where ΔS\Delta S is the change in entropy,
ΔQ\Delta Q is the change in the heat of the system,
TT is the temperature at which the reaction occurs.
The equation for the change in heat is as follows:
ΔQ=ΔHVΔP\Delta Q = \Delta H - V\Delta P ………..…… (2)
Where, ΔQ\Delta Q is the change in the heat of the system,
ΔH\Delta H is the change in the enthalpy of the system,
VV is the volume,
ΔP\Delta P is the change in the pressure.
The equation for the change in enthalpy is as follows:
ΔH=CPΔT\Delta H = {C_P}\Delta T ……...…… (3)
Where, ΔH\Delta H is the change in the enthalpy of the system,
CP{C_P} is the heat capacity at the constant pressure,
ΔT\Delta T is the change in the temperature.
From equation (1), equation (2) and equation (3),
ΔS=CPΔTVΔPT\Delta S = \dfrac{{{C_P}\Delta T - V\Delta P}}{T}
ΔS=CPΔTTVΔPT\Rightarrow \Delta S = \dfrac{{{C_P}\Delta T}}{T} - \dfrac{{V\Delta P}}{T}
ΔS=CPΔTTRΔPP\Rightarrow \Delta S = \dfrac{{{C_P}\Delta T}}{T} - \dfrac{{R\Delta P}}{P} (From the ideal gas equation, V/T=R/PV{\text{/}}T = R{\text{/}}P)
ΔS=CPΔTTRΔPP\Delta S = {C_P}\dfrac{{\Delta T}}{T} - R\dfrac{{\Delta P}}{P}
Thus,
ΔS=CPlnT2T1RlnP2P1\Delta S = {C_P}\ln \dfrac{{{T_2}}}{{{T_1}}} - R\ln \dfrac{{{P_2}}}{{{P_1}}} …… (4)
We know that for an ideal monatomic gas,
CP=5R2{C_P} = \dfrac{{5R}}{2} ………………... (5)
From equation (4) and equation (5),
ΔS=5R2lnT2T1RlnP2P1\Delta S = \dfrac{{5R}}{2}\ln \dfrac{{{T_2}}}{{{T_1}}} - R\ln \dfrac{{{P_2}}}{{{P_1}}} ………….…… (6)
Equation (6) is the equation for entropy in terms of temperature and pressure.
We are given that the temperature is doubled thus, T2=2×T1{T_2} = 2 \times {T_1}. The pressure becomes 2\sqrt {\text{2}} times thus, P2=2×P1{P_2} = \sqrt 2 \times {P_1}. Thus, equation (6) becomes as follows:
ΔS=5R2ln2×T1T1R×ln2×P1P1\Delta S = \dfrac{{5R}}{2}\ln \dfrac{{2 \times {T_1}}}{{{T_1}}} - R \times \ln \dfrac{{\sqrt 2 \times {P_1}}}{{{P_1}}}
ΔS=5R2ln2R×ln2\Delta S = \dfrac{{5R}}{2}\ln 2 - R \times \ln \sqrt 2
ΔS=5R2ln2R×ln(2)1/2\Rightarrow \Delta S = \dfrac{{5R}}{2}\ln 2 - R \times \ln {\left( 2 \right)^{{\text{1/2}}}}
ΔS=5R2ln2R2×ln2\Rightarrow \Delta S = \dfrac{{5R}}{2}\ln 2 - \dfrac{R}{2} \times \ln 2
ΔS=(5212)Rln2\Rightarrow\Delta S = \left( {\dfrac{5}{2} - \dfrac{1}{2}} \right)R\ln 2
ΔS=(42)Rln2\Rightarrow \Delta S = \left( {\dfrac{4}{2}} \right)R\ln 2
ΔS=2R ln2\Rightarrow \Delta S = {\text{2}}R{\text{ ln2}}
Thus, the entropy change in the process will be 2R ln2{\text{2}}R{\text{ ln2}}.

Thus, the correct option is (B) 2R ln2{\text{2}}R{\text{ ln2}}.

Note: The heat capacity at constant pressure contributes to the work done as well as the change in internal energy. It is denoted by CP{C_P}. For a monatomic ideal gas, the heat capacity at constant pressure is equal to 5R2\dfrac{{5R}}{2} where RR is the universal gas constant.