Two moles of an ideal gas occupy a volume V. The gas expands isothermally and reversibly to a volume
3V. (a) Is the velocity distribution changed by the isothermal expansion? Explain. (b) Use Eq.
(Microscopic state) to calculate the change in entropy of the gas. (c) Use Eq. (reversible isothermal
process) to calculate the change in entropy of the gas. Compare this result to that obtained in part (b).
Given
We are given an ideal gas with a number of moles n = 2.0 mol expands
isothermally from V1 to V2= 3V1.
Solution
(a) In the isothermal process, the temperature T is constant. As we know , the molecules in a gas don't all have the same speed, also this
speed depends on the temperature T therefore, the temperature is constant
or change, the distribution velocities of the molecules would not change.
where the distribution function depends on the
temperature T not on the change in temperature "\\Delta T" .
(b)
We are asked to calculate the change in entropy "\\Delta S"
which is expressed by
"\\Delta S=kln\\frac{w_2}{w_1}" .............(1)
Where k is Boltzmann's constant and equals"1.38x 10^{-23} J\/K"
w1 is the number of possible microscopic states for a given macroscopic
intial state and w2 is the same for the final state.
At the intial state w1, the gas has number of molecules N given by
"N = nN_A"
Where NA is Avogadro's number and equals 6.023x 1023molecules/mol
When the gas expands to three times volume 3V1 the number
of microscopic final state is greater than at initial state by factor 3N, so w2
will be
"w_2 = 3^Nw_1"
Now substitute this value of w2 into equation (1)
"\\Delta S = N k In 3 \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ (N = nN_A)\n\\\\\\Delta S = n N_A k In 3 \\ \\ \\ ..........(2)"
Now we can plug our values for NA, n and k into equation (2)
= 2.0 mol x 6.023 x 1023 molecules/mol x 1.38 x 10-23J/K x In 3
18.10J/K
="\\boxed{18.10 J\/k}"
(c)
We are asked to calculate the change in entropy "\\Delta S"
"\\Delta S= \\frac{Q}{T}" .................(3)
Where Q is the heat gained by the gas and could be calculated by the first
law of thermodynamics Q = W + "\\Delta U" where "\\Delta U" equals zero as the process
is isothermal. Therefore Q will be
"Q = W = nRT In\\frac{V_2}{ V_1} \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ \\ (V_2=3V_1)\\\\\nQ = W = nRT In\\frac{3V_1}{ V_1}\n\\\\ Q = W = nRT In3"
Where R is the gas constant and equals 8.314 J/mol.K
Now plug this equation for Q into equation (3) to get "\\Delta S"
"\\Delta S = nRT In3=2mole\\times8.314J\/mol.k\\times ln3\\\\\n\\Delta S= \\boxed{18.10 J\/k}"
The change in entropy is the same for part (b)
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