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Benzaldehyde, a flavoring agent, is obtained by the dehydrogenation of benzyl alcohol. $$ \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}(g) \rightleftharpoons \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}(g)+\mathrm{H}_{2}(g) $$ \(K\) for the reaction at \(250^{\circ} \mathrm{C}\) is \(0.56 .\) If \(1.50 \mathrm{~g}\) of benzyl alcohol is placed in a \(2.0-\mathrm{L}\) flask and heated to \(250^{\circ} \mathrm{C}\) (a) what is the partial pressure of the benzaldehyde when equilibrium is established? (b) how many grams of benzyl alcohol remain at equilibrium?

Short Answer

Expert verified
In summary, for the given reaction at equilibrium, the partial pressure of benzaldehyde is approximately \(0.214\: Atm\), and the amount of benzyl alcohol remaining is approximately \(0.425\:g\).

Step by step solution

01

Convert the given amount of benzyl alcohol into moles.

First, we need to determine the number of moles of benzyl alcohol. To do this, we will use the molar mass of benzyl alcohol, which is approximately \({108.14\:g/mol}\). $$ \text{moles of benzyl alcohol} = \frac{1.50\:g}{108.14\:g/mol} = 0.0139\:\text{mol} $$
02

Set up the initial and equilibrium concentrations in the reaction.

Next, let's set up the initial and equilibrium concentrations in a table. | | Benzyl Alcohol | Benzaldehyde | Hydrogen Gas | |----------|----------------|--------------|--------------| | Initial | 0.0139 mol | 0 mol | 0 mol | | Change | -x mol | +x mol | +x mol | | Equlbrm | 0.0139-x mol | x mol | x mol | Here, x represents the moles of benzyl alcohol that will reacted to form benzaldehyde and hydrogen gas.
03

Use the equilibrium constant expression to find the change in the concentrations of the substances and obtain the partial pressure of benzaldehyde.

Now we will use the equilibrium constant expression to solve for x, and then calculate the equilibrium partial pressure of benzaldehyde. The partial pressure of each substance can be calculated using the ideal gas law, \(PV=nRT\). For this problem, the total volume is \(2.0\:L\), and the temperature is \(250^\circ C = 523\:K\). The gas constant R in terms of pressure is \(0.0821 \: Atmosphere \cdot L / mol \cdot K\). $$ K = \frac{P_{\text{benzaldehyde}}\:P_{H_2}}{P_{\text{benzylalcohol}}} \:\Rightarrow\: [0.56] = \frac{x^2/2}{(0.0139-x)/2} $$ Solving for x, we get: $$ x \approx 0.00997\: \text{mol} $$ Now, we can find the partial pressure of benzaldehyde using the formula we derived above: $$ P_{\text{benzaldehyde}} = \frac{nRT}{V} =\frac{(0.00997\:mol)(0.0821\:Atm\:L^1 \cdot mol^{-1} \cdot K^{-1})(523\:K)}{2.0\:L} $$ $$ \Rightarrow\: P_{\text{benzaldehyde}} \approx 0.214\:Atm $$ So, the partial pressure of benzaldehyde is approximately \(0.214\: Atm\)
04

Calculate the remaining amount of benzyl alcohol in grams.

Now, we will determine the moles of benzyl alcohol remaining at equilibrium, and convert it into grams. From Step 3, we know x is approximately \(0.00997\:\text{mol}\). $$ \text{moles of benzylalcohol at equilibrium} = \text{initial moles - x} = 0.0139 - 0.00997 = 0.00393\: \text{mol} $$ $$ \text{grams of benzylalcohol remaining} = 0.00393 \: \text{mol} \times 108.14 \: \text{g/mol} \approx 0.425\:g $$ Therefore, approximately \(0.425\:g\) of benzyl alcohol remains at equilibrium.

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Most popular questions from this chapter

At \(500^{\circ} \mathrm{C}, K\) for the formation of ammonia from nitrogen and hydrogen gases is \(1.5 \times 10^{-5}\). $$\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons 2 \mathrm{NH}_{3}(g)$$ Calculate the equilibrium partial pressure of hydrogen if the equilibrium partial pressures of ammonia and nitrogen are \(0.015 \mathrm{~atm}\) and $1.2 \mathrm{~atm}$, respectively.

Consider the equilibrium $$ \mathrm{H}_{2}(g)+\mathrm{S}(s) \rightleftharpoons \mathrm{H}_{2} \mathrm{~S}(g) $$ When this system is at equilibrium at \(25^{\circ} \mathrm{C}\) in a \(2.00-\mathrm{L}\) container, \(0.120 \mathrm{~mol}\) of \(\mathrm{H}_{2}, 0.034 \mathrm{~mol}\) of \(\mathrm{H}_{2} \mathrm{~S},\) and \(0.4000 \mathrm{~mol}\) of \(\mathrm{S}\) are present. When the temperature is increased to \(35^{\circ} \mathrm{C}\), the partial pressure of \(\mathrm{H}_{2}\) increases to \(1.56 \mathrm{~atm} .\) (a) What is \(K\) for the reaction at \(25^{\circ} \mathrm{C} ?\) (b) What is \(K\) for the reaction at \(35^{\circ} \mathrm{C} ?\)

Consider the decomposition of ammonium hydrogen sulfide: $$ \mathrm{NH}_{4} \mathrm{HS}(s) \rightleftharpoons \mathrm{NH}_{3}(g)+\mathrm{H}_{2} \mathrm{~S}(g) $$ In a sealed flask at \(25^{\circ} \mathrm{C}\) are \(10.0 \mathrm{~g}\) of \(\mathrm{NH}_{4} \mathrm{HS}\), ammonia with a partial pressure of \(0.692 \mathrm{~atm},\) and \(\mathrm{H}_{2} \mathrm{~S}\) with a partial pressure of \(0.0532 \mathrm{~atm}\). When equilibrium is established, it is found that the partial pressure of ammonia has increased by 12.4\%. Calculate \(K\) for the decomposition of \(\mathrm{NH}_{4} \mathrm{HS}\) at \(25^{\circ} \mathrm{C}\).

Sulfur oxychloride, \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\), decomposes to sulfur dioxide and chlorine gases. $$ \mathrm{SO}_{2} \mathrm{Cl}_{2}(g) \rightleftharpoons \mathrm{SO}_{2}(g)+\mathrm{Cl}_{2}(g) $$ At a certain temperature, the equilibrium partial pressures of \(\mathrm{SO}_{2}, \mathrm{Cl}_{2},\) and \(\mathrm{SO}_{2} \mathrm{Cl}_{2}\) are \(1.88 \mathrm{~atm}, 0.84 \mathrm{~atm},\) and \(0.27 \mathrm{~atm}\) respectively. (a) What is \(K\) at that temperature? (b) Enough \(\mathrm{Cl}_{2}\) condenses to reduce its partial pressure to 0.68 atm. What are the partial pressures of all gases when equilibrium is reestablished?

At \(800^{\circ} \mathrm{C}, K=2.2 \times 10^{-4}\) for the following reaction $$ 2 \mathrm{H}_{2} \mathrm{~S}(g) \rightleftharpoons 2 \mathrm{H}_{2}(g)+\mathrm{S}_{2}(g) $$ Calculate \(K\) at \(800^{\circ} \mathrm{C}\) for (a) the synthesis of one mole of \(\mathrm{H}_{2} \mathrm{~S}\) from \(\mathrm{H}_{2}\) and \(\mathrm{S}_{2}\) gases. (b) the decomposition of one mole of \(\mathrm{H}_{2} \mathrm{~S}\) gas.

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