Homework #2 (Chapter 4, 5, 6)
Due date : June 5th, 2023
1. Pressure was exerted with a piston on molten naphthalene at 95°C. The vapour pressure of
naphthalene under 1.0 bar is 2.0 kPa and its density is 0.962 g cm−3. What is its vapour pressure
when the pressure on the liquid is 15 MPa? (Molar mass of naphthalene: 128.17 g mol−1,
R=8.3145 J K-1 mol-1)
2. The vapour pressure of dichloromethane at 24.1°C is 53.3 kPa and its enthalpy of vaporization
is 28.7 kJ mol−1. Estimate the temperature at which its vapour pressure is 70.0 kPa. (R=8.3145
J K-1 mol-1)
3. The vapour pressure of a liquid between 15°C and 35°C fits the expression log(p/Torr) = 8.750
− 1625/(T/K). Calculate (a) the enthalpy of vaporization and (b) the normal boiling point of
the liquid. (R=8.3145 J K-1 mol-1)
4. Calculate the melting point of ice under a pressure of 10 MPa. Assume that the density of ice
under these conditions is approximately 0.915 g cm−3 and that of liquid water is 0.998 g cm−3.
5. The vapour pressure of 2-propanol is 50.00 kPa at 338.8°C, but it fell to 49.62 kPa when 8.69
g of an involatile organic compound was dissolved in 250 g of 2-propanol. Calculate the molar
mass of the compound. (Molar mass of 2-propanol: 60.096 g mol-1)
6. By measuring the equilibrium between liquid and vapour phases of an acetone(A)/methanol(M)
solution at 57.2°C at 1.00 atm, it was found that xA = 0.400 when yA = 0.516. Calculate the
activities and activity coefficients of both components in this solution on the Raoult’s law basis.
The vapour pressures of the pure components at this temperature are: p*A = 105 kPa and p*M
= 73.5 kPa. (xA is the mole fraction in the liquid and yA the mole fraction in the vapour,)
7. In the gas-phase reaction 2A + B ⇌ 3C + 2D, it was found that, when 1.00 mol A, 2.00 mol
B, and 1.00 mol D were mixed and allowed to come to equilibrium at 25°C, the resulting
mixture contained 0.90 mol C at a total pressure of 1.00 bar. Calculate (a) the mole fractions
of each species at equilibrium, (b) Kx, (c) K, and (d) ΔrG⊖.
8. For CaF2(s) ⇌ Ca2+(aq) + 2F−(aq), K = 3.9 × 10−11 at 25°C and the standard Gibbs energy of
formation of CaF2(s) is −1167 kJ mol−1. Calculate the standard Gibbs energy of formation of
CaF2(aq).
9. The dissociation vapour pressure of NH4Cl at 427°C is 608 kPa but at 459°C it has risen to
1115 kPa. Calculate (a) the equilibrium constant, (b) the standard reaction Gibbs energy, (c)
the standard enthalpy, (d) the standard entropy of dissociation, all at 427°C. Assume that the
vapour behaves as a perfect gas and that ΔH⊖ and ΔS⊖ are independent of temperature in the
range given.
10. Calculate the equilibrium constants of the following reactions at 25°C from standard
potential data:
(a) Sn(s) + Sn4+ (aq) ⇌ 2 Sn2+ (aq)
(b) Sn(s) + 2 AgCl(s) ⇌ SnCl2(aq) + 2 Ag(s)