For an ideal solution, the total vapour pressure is given by Raoult’s Law, which states:
Ptotal = Pbenzene + Ptoluene
Where:
Here, P0 benzene and P0 toluene are the vapour pressures of pure benzene and toluene, and Xbenzene and Xtoluene are the mole fractions of benzene and toluene, respectively.
The mole fraction of benzene Xbenzene is related to the total vapour pressure by the equation:
Ptotal = P0 benzene · Xbenzene + P0 toluene · (1 − Xbenzene)
Substitute the given values into the equation:
0.3 = 0.5 · Xbenzene + 0.2 · (1 − Xbenzene)
Simplify and solve for Xbenzene:
0.3 = 0.5 · Xbenzene + 0.2 − 0.2 · Xbenzene
0.3 − 0.2 = 0.5 · Xbenzene − 0.2 · Xbenzene
0.1 = 0.3 · Xbenzene
Xbenzene = \( \frac{0.1}{0.3} = 0.34 \)
Thus, the mole fraction of benzene in the mixture is 0.34.
For a single component system at vapor-liquid equilibrium, the extensive variables A, V, S and N denote the Helmholtz free energy, volume, entropy, and number of moles, respectively, in a given phase. If superscripts \( (\nu) \) and \( (\ell) \) denote the vapor and liquid phase, respectively, the relation that is NOT CORRECT is