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Question: How would you use the van der Waals equation of state to calculate the pressure of \(3.60\)mol of \[...

How would you use the van der Waals equation of state to calculate the pressure of 3.603.60mol of H2O{H_2}O at 4253K4253K in a 5.90L5.90L vessel?

Explanation

Solution

We have to know that an equation that deals with the relationship between the pressure, volume, temperature, and amount of real gases is defined as van der Waals equation of gases. In the modifications which are made related to equation of ideal gas for real gases, the reduction in pressure is because of forces of attractions among the molecules is straightly proportional to n2V2\dfrac{{{n^2}}}{{{V^2}}}

Complete step by step answer:
Given data contains,
The number of moles = 3.60mol3.60mol
Gas constant = 0.08314lbarLK1mol10.08314lbar \cdot L \cdot {K^{ - 1}}mo{l^{ - 1}}
Temperature = 453K453K
Volume = 5.90L5.90L
a = 5.536 barL2mol25.536{\text{ }}bar \cdot {L^2}mo{l^{ - 2}}
b = 0.030 49 Lmol10.030{\text{ }}49{\text{ }}L \cdot mo{l^{ - 1}}
We could substitute the values of ideal volume and ideal pressure in ideal gas equation PV=nRTPV = nRT, the modified expression could be written as,
(P+an2V2)(vnb)=nRT\left( {P + a\dfrac{{{n^2}}}{{{V^2}}}} \right)\left( {v - nb} \right) = nRT
We can rearrange the above expression as,
(P+an2V2)=nRT(vnb)\left( {P + \dfrac{{a{n^2}}}{{{V^2}}}} \right) = \dfrac{{nRT}}{{\left( {v - nb} \right)}}
P=nRT(vnb)n2aV2P = \dfrac{{nRT}}{{\left( {v - nb} \right)}} - \dfrac{{{n^2}a}}{{{V^2}}}
Here the pressure is indicated by P.
The molar volume is indicated by V.
The temperature of the given sample of the gas is indicated by T.
The gas constant is indicated by R.
van der waals constant is indicated by a and b.
n indicated the moles of the gas.
Let us now substitute the given values in the above expression of Vander Waals equation as
P=nRT(vnb)n2aV2P = \dfrac{{nRT}}{{\left( {v - nb} \right)}} - \dfrac{{{n^2}a}}{{{V^2}}}
Now we can substitute the known values we get,
P=(3.60mol)(0.08314barLK1mol1)×(453K)(5.90L3.60mol×0.03049Lmol2)P = \dfrac{{\left( {3.60mol} \right)\left( {0.08314\,bar\,L \cdot {K^{ - 1}}mo{l^{ - 1}}} \right) \times \left( {453K} \right)}}{{\left( {5.90L - 3.60mol \times 0.03049\,L \cdot mo{l^{ - 2}}} \right)}}
P=135.6bar5.900.10982.061barP = \dfrac{{135.6bar}}{{5.90 - 0.1098}} - 2.061bar
P=23.42bar2.061barP = 23.42bar - 2.061bar
On simplification we get,
P=21.4barP = 21.4bar

The pressure is calculated as 21.4bar21.4bar.

Note: Now we can discuss the certain of the advantages of van der Waals equation are,
Determines the behaviour of gases better than the ideal gas equation.
Applicable for gases and fluids.
Certain of the disadvantages of van der Waals equation are,
We could get better results of all real gases only above critical temperature using van der Waals equation.
Vander Waals completely fails in the transformation phase of gas to the liquid below a critical temperature.