The normal boiling point for ethyl alcohol is \(78.4^{\circ} \mathrm{C} .5^{\circ}\) for \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(g)\) is \(282.7 \mathrm{~J} / \mathrm{mol} \cdot \mathrm{K}\). At what temperature is the vapor pressure of ethyl alcohol \(357 \mathrm{~mm} \mathrm{Hg} ?\)

Short Answer

Expert verified
Answer: The temperature at which the vapor pressure of ethyl alcohol is 357 mm Hg is approximately 66.4°C.

Step by step solution

01

Find the enthalpy of vaporization at T = 78.4°C using molar heat capacity

Since we are given the molar heat capacity at constant volume for C2H5OH(g), we can find the enthalpy of vaporization at T1 = 78.4°C (the given normal boiling point) using the following equation: \(\Delta H_{vap} = C_{v}(T_{2} - T_{1}) \text{(Assumption: constant molar heat capacity)}\) We have the molar heat capacity and T1, but we need to find T2. At the boiling point, the vapor pressure of the liquid is equal to the atmospheric pressure. Assuming standard conditions, the atmospheric pressure is 1 atm, which can be converted to mm Hg: \(1 \ \text{atm} = 760 \ \text{mm Hg}\) Since we know the vapor pressure is 357 mm Hg, we can find T2 by solving for it using the Clausius-Clapeyron equation. However, we first need the enthalpy of vaporization.
02

Convert temperatures to Kelvin

To use the Clausius-Clapeyron equation and find the enthalpy of vaporization, we need to convert the given Celsius temperatures to Kelvin: \(T_{1(K)} = T_{1(°C)} + 273.15\) \(T_{1(K)} = 78.4 + 273.15 = 351.55 \ \text{K}\)
03

Calculate the enthalpy of vaporization

Now we can substitute the conversion factor from Step 2 into the first equation for enthalpy of vaporization: \(\Delta H_{vap} = C_{v}(T_{2} - T_{1})\) \(\Delta H_{vap} = 282.7 \ \text{J/mol K} \cdot (760 - 351.55) \ \text{K}\) \(\Delta H_{vap} \approx 115189.485 \ \text{J/mol}\)
04

Apply the Clausius-Clapeyron equation to find T2

With all necessary values to use the Clausius-Clapeyron equation, we can solve for the temperature at which the vapor pressure of ethyl alcohol is 357 mm Hg: \(ln\frac{P_2}{P_1}=-\frac{\Delta H_{vap}}{R}\left(\frac{1}{T2}-\frac{1}{T1}\right)\) \(ln\frac{357}{760}=-\frac{115189.485}{8.314}\left(\frac{1}{T2}-\frac{1}{351.55}\right)\) Now, solve for the temperature T2: \(T2 \approx 339.55 \ \text{K}\)
05

Convert the final temperature to Celsius

Finally, we'll convert the temperature back to Celsius for the final answer: \(T_{2(°C)} = T_{2(K)} - 273.15\) \(T_{2(°C)} = 339.55 - 273.15\) \(T_{2(°C)} \approx 66.4 ^{\circ}\text{C}\) The temperature at which the vapor pressure of ethyl alcohol is 357 mm Hg is approximately 66.4°C.

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Most popular questions from this chapter

Predict the sign of \(\Delta S^{\circ}\) for each of the following reactions. (a) \(\mathrm{H}_{2}(g)+\mathrm{Ni}^{2+}(a q) \longrightarrow 2 \mathrm{H}^{+}(a q)+\mathrm{Ni}(s)\) (b) \(\mathrm{Cu}(s)+2 \mathrm{H}^{+}(a q) \longrightarrow \mathrm{H}_{2}(g)+\mathrm{Cu}^{2+}(a q)\) (c) \(\mathrm{N}_{2} \mathrm{O}_{4}(g) \longrightarrow 2 \mathrm{NO}_{2}(g)\)

Earlier civilizations smelted iron from ore by heating it with charcoal from a wood fire: $$ 2 \mathrm{Fe}_{2} \mathrm{O}_{3}(s)+3 \mathrm{C}(s) \longrightarrow 4 \mathrm{Fe}(s)+3 \mathrm{CO}_{2}(g) $$ (a) Obtain an expression for \(\Delta G^{\circ}\) as a function of temperature. Prepare a table of \(\Delta G^{\circ}\) values at \(100-\mathrm{K}\) intervals between \(100 \mathrm{~K}\) and \(500 \mathrm{~K}\) (b) Calculate the lowest temperature at which the smelting could be carried out.

For the reaction $$ 2 \mathrm{Cl}^{-}(a q)+\mathrm{Br}_{2}(l) \longrightarrow \mathrm{Cl}_{2}(g)+2 \mathrm{Br}^{-}(a q) $$ calculate the temperature at which \(\Delta G^{\circ}=0 .\)

Show by calculation whether the reaction $$ \mathrm{HC}_{2} \mathrm{H}_{3} \mathrm{O}_{2}(a q) \rightleftharpoons \mathrm{H}^{+}(a q)+\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{O}_{2}^{-}(a q) \quad \Delta G^{\circ}=+27.2 \mathrm{~kJ} $$ is spontaneous at \(25^{\circ} \mathrm{C}\) (a) when \(\left[\mathrm{H}^{+}\right]=\left[\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{O}_{2}^{-}\right]=0.85 M_{;}\left[\mathrm{HC}_{2} \mathrm{H}_{3} \mathrm{O}_{2}\right]=0.15 \mathrm{M}\). (b) when \(\left[\mathrm{H}^{+}\right]=\left[\mathrm{C}_{2} \mathrm{H}_{3} \mathrm{O}_{2}^{-}\right]=2.0 \times 10^{-3} \mathrm{M} ;\left[\mathrm{HC}_{2} \mathrm{H}_{3} \mathrm{O}_{2}\right]=1.0 \mathrm{M}\).

Theoretically, one can obtain zinc from an ore containing zinc sulfide, \(\mathrm{ZnS}\), by the reaction $$ \mathrm{ZnS}(s) \longrightarrow \mathrm{Zn}(s)+\mathrm{S}(s) $$ (a) Show by calculation that this reaction is not feasible at \(25^{\circ} \mathrm{C}\). (b) Show that by coupling the above reaction with the reaction $$ \mathrm{S}(s)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{SO}_{2}(g) $$ the overall reaction, in which \(\mathrm{Zn}\) is obtained by roasting in oxygen, is feasible at \(25^{\circ} \mathrm{C}\).

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