The vapor pressure of a volatile liquid can be determined by slowly bubbling a known volume of gas through it at a known temperature and pressure. In an experiment, \(5.00 \mathrm{~L}\) of \(\mathrm{N}_{2}\) gas is passed through \(7.2146 \mathrm{~g}\) of liquid benzene, \(\mathrm{C}_{6} \mathrm{H}_{6}\), at \(26.0{ }^{\circ} \mathrm{C}\). The liquid remaining after the experiment weighs \(5.1493 \mathrm{~g}\). Assuming that the gas becomes saturated with benzene vapor and that the total gas volume and temperature remain constant, what is the vapor pressure of the benzene in torr?

Short Answer

Expert verified
The vapor pressure of benzene in this experiment is approximately \(98.91\mathrm{~torr}\).

Step by step solution

01

Calculate the mass of evaporated benzene

First, we need to find the mass of benzene that evaporated during the experiment. This can be found by taking the difference between the initial mass and the final mass. $$\text{Mass of evaporated benzene} = \text{Initial mass} - \text{Final mass}$$ $$\text{Mass of evaporated benzene} = 7.2146\mathrm{~g} - 5.1493\mathrm{~g} = 2.0653\mathrm{~g}$$
02

Convert the mass of evaporated benzene into moles

To calculate the moles of evaporated benzene, we will use the molar mass of benzene which is approximately \(78.11\mathrm{~g/mol}\). $$\text{Moles of evaporated benzene} = \frac{\text{Mass of evaporated benzene}}{\text{Molar mass of benzene}}$$ $$\text{Moles of evaporated benzene} = \frac{2.0653\mathrm{~g}}{78.11\mathrm{~g/mol}} = 0.02645\mathrm{~mol}$$
03

Convert the given temperature to Kelvin

Before we can use the Ideal Gas Law, we need to convert the given temperature from Celsius to Kelvin. $$T(K) = T(^{\circ}\mathrm{C}) + 273.15$$ $$T(K) = 26.0{ }^{\circ} \mathrm{C} + 273.15 = 299.15\mathrm{~K}$$
04

Apply the Ideal Gas Law to find the partial pressure of benzene

Now that we have the moles of evaporated benzene and the temperature in Kelvin, we can use the Ideal Gas Law to determine the vapor pressure (partial pressure) of benzene in the gaseous mixture. The Ideal Gas Law is as follows: $$PV = nRT$$ We'll rearrange the equation to find the partial pressure of benzene, where \(P\) is the partial pressure, \(n\) is the moles of evaporated benzene, \(R\) is the ideal gas constant, \(T\) is the temperature in Kelvin, and \(V\) is the volume. $$P = \frac{nRT}{V}$$ For our calculation, we will use the gas constant \(R = 62.363\mathrm{~L\cdot torr/mol\cdot K}\). The given volume of the gas mixture is \(5.00\mathrm{~L}\). $$P_\mathrm{benzene} = \frac{(0.02645\mathrm{~mol})(62.363\mathrm{~L\cdot torr/mol\cdot K})(299.15\mathrm{~K})}{5.00\mathrm{~L}} = 98.91\mathrm{~torr}$$ Therefore, the vapor pressure of benzene in this experiment is approximately \(98.91\mathrm{~torr}\).

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Most popular questions from this chapter

If \(42.0 \mathrm{~kJ}\) of heat is added to a 32.0 -g sample of liquid methane under 1 atm of pressure at a temperature of \(-170{ }^{\circ} \mathrm{C},\) what are the final state and temperature of the methane once the system equilibrates? Assume no heat is lost to the surroundings. The normal boiling point of methane is \(-161.5^{\circ} \mathrm{C}\). The specific heats of liquid and gaseous methane are 3.48 and \(2.22 \mathrm{~J} / \mathrm{g}-\mathrm{K},\) respectively. [Section 11.4\(]\)

(a) How does the average kinetic energy of molecules compare with the average energy of attraction between molecules in solids, liquids, and gases? (b) Why does increasing the temperature cause a solid substance to change in succession from a solid to a liquid to a gas? (c) What happens to a gas if you put it under extremely high pressure?

As the intermolecular attractive forces between molecules increase in magnitude, do you expect each of the following to increase or decrease in magnitude? (a) vapor pressure, (b) heat of vaporization, (c) boiling point, (d) freezing point, (e) viscosity, (f) surface tension, (g) critical temperature.

Ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) melts at \(-114{ }^{\circ} \mathrm{C}\) and boils at \(78{ }^{\circ} \mathrm{C}\). The enthalpy of fusion of ethanol is \(5.02 \mathrm{~kJ} / \mathrm{mol},\) and its enthalpy of vaporization is \(38.56 \mathrm{~kJ} / \mathrm{mol}\). The specific heats of solid and liquid ethanol are \(0.97 \mathrm{~J} / \mathrm{g}-\mathrm{K}\) and \(2.3 \mathrm{~J} / \mathrm{g}-\mathrm{K},\) respectively. (a) How much heat is required to convert \(42.0 \mathrm{~g}\) of ethanol at \(35^{\circ} \mathrm{C}\) to the vapor phase at \(78{ }^{\circ} \mathrm{C} ?\) (b) How much heat is required to convert the same amount of ethanol at \(-155^{\circ} \mathrm{C}\) to the vapor phase at \(78^{\circ} \mathrm{C}\) ?

In dichloromethane, \(\mathrm{CH}_{2} \mathrm{Cl}_{2}(\mu=1.60 \mathrm{D})\), the dispersion force contribution to the intermolecular attractive forces is about five times larger than the dipole-dipole contribution. Compared to \(\mathrm{CH}_{2} \mathrm{Cl}_{2}\), would you expect the relative importance of the dipole-dipole contribution to increase or decrease (a) in dibromomethane \((\mu=1.43 \mathrm{D}),(\mathbf{b})\) in difluoromethane \((\mu=1.93 \mathrm{D}) ?\) Explain.

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