A "canned heat" product used to warm buffet dishes consists of a homogeneous mixture of ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) and paraffin, which has an average formula of $\mathrm{C}_{24} \mathrm{H}_{50}\(. What mass of \)\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}$ should be added to \(620 \mathrm{~kg}\) of the paraffin to produce $1.07 \mathrm{kPa}\( of ethanol vapor pressure at \)35^{\circ} \mathrm{C}$ ? The vapor pressure of pure ethanol at \(35^{\circ} \mathrm{C}\) is \(13.3 \mathrm{kPa}\).

Short Answer

Expert verified
The mass of ethanol to be added to 620 kg of paraffin to produce 1.07 kPa of ethanol vapor pressure at 35°C is approximately 7,389.02 g.

Step by step solution

01

Understanding Raoult's Law

Raoult's law states that the partial pressure of a component in a mixture is equal to the mole fraction of that component multiplied by the vapor pressure of the pure component. Mathematically, it can be represented as: \( P_A = x_A P_A^* \) where, \(P_A\) is the partial pressure of component A in the mixture, \(x_A\) is the mole fraction of component A in the mixture, and \(P_A^*\) is the vapor pressure of pure component A.
02

Determine the mole fraction of ethanol

In the given problem, the vapor pressure of ethanol in the mixture is 1.07 kPa, and the vapor pressure of pure ethanol is 13.3 kPa. We can use Raoult's law to determine the mole fraction of ethanol in the mixture: \(1.07 \mathrm{kPa} = x_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} \times 13.3 \mathrm{kPa} \) Solving for \( x_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} \): \( x_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} = 0.0805 \)
03

Calculate the moles of paraffin and ethanol

To find the mass of ethanol that should be added to the mixture, we need to determine the moles of paraffin and ethanol. The mass of paraffin is given as 620 kg, and the average molecular formula of paraffin is C24H50. First, let's find the molar mass of paraffin: \( \mathrm{MM}_{\mathrm{C}_{24}\mathrm{H}_{50}} = 24 \times 12.01 + 50 \times 1.01 = 338.34 \hspace{2mm} \mathrm{g/mol} \) Now, we can find the moles of paraffin: \(\mathrm{moles}_{\mathrm{C}_{24}\mathrm{H}_{50}} = \frac{620,000 \hspace{2mm} \mathrm{g}}{338.34 \hspace{2mm} \mathrm{g/mol}} = 1833.49 \hspace{2mm} \mathrm{mol} \) Now, let's find the moles of ethanol using the mole fraction of ethanol: \( \frac{\mathrm{moles}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}}}{\mathrm{moles}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} + \mathrm{moles}_{\mathrm{C}_{24}\mathrm{H}_{50}}} = 0.0805 \) Solving for the moles of ethanol: \( \mathrm{moles}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} = 0.0805 \times \mathrm{moles}_{\mathrm{C}_{24}\mathrm{H}_{50}} / (1 - 0.0805) = 160.41 \hspace{2mm} \mathrm{mol} \)
04

Calculate the mass of ethanol to be added

Finally, we can find the mass of ethanol to be added by using the molar mass of ethanol, which is: \( \mathrm{MM}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} = 2 \times 12.01 + 6 \times 1.01 + 1 \times 16 = 46.07 \hspace{2mm} \mathrm{g/mol} \) The mass of ethanol to be added is: \( \mathrm{mass}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} = \mathrm{moles}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} \times \mathrm{MM}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} \) \( \mathrm{mass}_{\mathrm{C}_{2}\mathrm{H}_{5}\mathrm{OH}} = 160.41 \hspace{2mm} \mathrm{mol} \times 46.07 \hspace{2mm} \mathrm{g/mol} = 7,389.02 \hspace{2mm} \mathrm{g} \) So, 7,389.02 g of ethanol should be added to 620 kg of the paraffin to produce 1.07 kPa of ethanol vapor pressure at 35°C.

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Most popular questions from this chapter

The following table presents the solubilities of several gases in water at \(25^{\circ} \mathrm{C}\) under a total pressure of gas and water vapor of 101.3 kPa. (a) What volume of \(\mathrm{CH}_{4}(g)\) under standard conditions of temperature and pressure is contained in \(4.0 \mathrm{~L}\) of a saturated solution at \(25^{\circ} \mathrm{C} ?\) (b) The solubilities (in water) of the hydrocarbons are as follows: methane \(<\) ethane \(<\) ethylene. Is this because ethylene is the most polar molecule? (c) What intermolecular interactions can these hydrocarbons have with water? (d) Draw the Lewis dot structures for the three hydrocarbons. Which of these hydrocarbons possess \(\pi\) bonds? Based on their solubilities, would you say \(\pi\) bonds are more or less polarizable than \(\sigma\) bonds? (e) Explain why NO is more soluble in water than either \(\mathrm{N}_{2}\) or \(\mathrm{O}_{2} .\) (f) \(\mathrm{H}_{2} \mathrm{~S}\) is more water-soluble than almost all the other gases in table. What intermolecular forces is $\mathrm{H}_{2} \mathrm{~S}\( likely to have with water? \)(\mathbf{g}) \mathrm{SO}_{2}$ is by far the most water-soluble gas in table. What intermolecular forces is \(\mathrm{SO}_{2}\) likely to have with water? $$ \begin{array}{lc} \hline \text { Gas } & \text { Solubility (mM) } \\ \hline \mathrm{CH}_{4} \text { (methane) } & 1.3 \\ \mathrm{C}_{2} \mathrm{H}_{6} \text { (ethane) } & 1.8 \\ \mathrm{C}_{2} \mathrm{H}_{4} \text { (ethylene) } & 4.7 \\ \mathrm{~N}_{2} & 0.6 \\ \mathrm{O}_{2} & 1.2 \\ \mathrm{NO} & 1.9 \\ \mathrm{H}_{2} \mathrm{~S} & 99 \\ \mathrm{SO}_{2} & 1476 \\ \hline \end{array} $$

Indicate whether each statement is true or false: (a) The higher the temperature, the more soluble most gases are in water. (b) The higher the temperature, the more soluble most ionic solids are in water. (c) As you cool a saturated solution from high temperature to low temperature, solids start to crystallize out of solution if you achieve a supersaturated solution. (d) If you take a saturated solution and raise its temperature, you can (usually) add more solute and make the solution even more concentrated.

During a person's typical breathing cycle, the \(\mathrm{CO}_{2}\) concentration in the expired air rises to a peak of \(4.6 \%\) by volume. (a) Calculate the partial pressure of the \(\mathrm{CO}_{2}\) in the expired air at its peak, assuming \(101.3 \mathrm{kPa}\) pressure and a body temperature of $37^{\circ} \mathrm{C}\(. (b) What is the molarity of the \)\mathrm{CO}_{2}$ in the expired air at its peak, assuming a body temperature of \(37^{\circ} \mathrm{C} ?\)

You take a sample of water that is at room temperature and in contact with air and put it under a vacuum. Right away, you see bubbles leave the water, but after a little while, the bubbles stop. As you keep applying the vacuum, more bubbles appear. A friend tells you that the first bubbles were water vapor, and the low pressure had reduced the boiling point of water, causing the water to boil. Another friend tells you that the first bubbles were gas molecules from the air (oxygen, nitrogen, and so forth) that were dissolved in the water. Which friend is mostly likely to be correct? What, then, is responsible for the second batch of bubbles? [Section 13.4]

Describe how you would prepare each of the following aqueous solutions: \((\mathbf{a}) 1.50 \mathrm{~L}\) of $0.110 \mathrm{M}\left(\mathrm{NH}_{4}\right)_{2} \mathrm{SO}_{4}$ solution, starting with solid $\left(\mathrm{NH}_{4}\right)_{2} \mathrm{SO}_{4} ;(\mathbf{b}) 225 \mathrm{~g}\( of a solution that is \)0.65 \mathrm{~m}\( in \)\mathrm{Na}_{2} \mathrm{CO}_{3},\( starting with the solid solute; \)(\mathbf{c}) 1.20$ \(\mathrm{L}\) of a solution that is $15.0 \% \mathrm{~Pb}\left(\mathrm{NO}_{3}\right)_{2}$ by mass (the density of the solution is \(1.16 \mathrm{~g} / \mathrm{mL}\) ), starting with solid solute; (d) a \(0.50 \mathrm{M}\) solution of \(\mathrm{HCl}\) that would just neutralize \(5.5 \mathrm{~g}\) of \(\mathrm{Ba}(\mathrm{OH})_{2}\) starting with $6.0 \mathrm{MHCl}$.

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