For the reaction below, \(K_{\mathrm{p}}=1.16\) at \(800 .^{\circ} \mathrm{C}\) $$\mathrm{CaCO}_{3}(s) \rightleftharpoons \mathrm{CaO}(s)+\mathrm{CO}_{2}(g)$$ If a 20.0 -g sample of \(\mathrm{CaCO}_{3}\) is put into a 10.0 -L container and heated to \(800 .^{\circ} \mathrm{C},\) what percentage by mass of the \(\mathrm{CaCO}_{3}\) will react to reach equilibrium?

Short Answer

Expert verified
The percentage of calcium carbonate reacting to reach equilibrium by mass is approximately 25.26% at 800°C with Kp = 1.16.

Step by step solution

01

Calculate the initial amount of calcium carbonate in moles

We are given a 20.0 g sample of CaCO3, using its molar mass, we can convert this mass to moles: Molar mass of CaCO3 = 40.08 (for Ca) + 12.01 (for C) + 3 * 16.00 (for O) = 100.09 g/mol Now, calculate the moles of CaCO3: moles of CaCO3 = (20.0 g) / (100.09 g/mol) = 0.2 mol
02

Write the expression for Kp definition and ICE table

The reaction at equilibrium can be described by the equilibrium constant Kp, which is given as 1.16. Write the expression for Kp: \(K_p = \frac{[CO_2]^{\delta n_{CO_2}}}{[CaCO_3]^{\delta n_{CaCO_3}}[CaO]^{\delta n_{CaO}}}\) In this case, since CaCO3 and CaO are in solid state and their concentrations remain constant, their activity is considered as 1. We can simplify the expression: \(K_p = [CO_2]\) Now, let's create an ICE (Initial - Change - Equilibrium) table for the reaction: | | CaCO3 | CaO | CO2 | |:----------:|:-----:|:------:|:-----:| | Initial | 0.2 | 0 | 0 | | Change | -x | x | x | | Equilibrium| 0.2-x | x | x | Where x is the amount of CaCO3 that reacts to reach equilibrium.
03

Calculate the equilibrium partial pressure of CO2

We can now calculate the equilibrium partial pressure of CO2. We know that Kp = [CO2] and that the volume of the container is 10.0 L. The relationship between partial pressure and concentration is given by: \(P_{CO2} = \frac{n_{CO2}RT}{V}\) Where R is the ideal gas constant = 0.0821 L atm/mol K and T is the temperature in Kelvin (in this case, 800°C = 1073.15 K). We can express the equilibrium concentration of CO2 in terms of the partial pressure as: \([CO_2] = \frac{P_{CO2}V}{n_{CO2}R}\) Substitute this into the Kp expression: \(K_p = \frac{P_{CO2}V}{n_{CO2}R}\) Solve for P_CO2: \(P_{CO2} = K_p n_{CO2}R\) Now, substitute the values of Kp, n_CO2 (which is x), R, and V: \(P_{CO2} = (1.16)(x)(0.0821)(1073.15)\)
04

Calculate the amount of reacted CaCO3 to reach equilibrium

We can use the relationship between partial pressure and concentration to find the value of x, which represents the amount of CaCO3 that reacted to reach equilibrium: \(P_{CO2} = x*RT/V\) \(x = \frac{P_{CO2}V}{RT}\) Plug in the values for P_CO2, R, T, and V: \(x = \frac{(1.16)(0.0821)(1073.15)(10.0)}{0.2}\) x = 0.05051 mol
05

Calculate the percentage of reacted CaCO3 and express it by mass

Now that we have the moles of reacted CaCO3, we can calculate the percentage of the initial 20.0 g sample that reacted: Percentage reacted = \(\frac{reacted \:moles}{initial\: moles} \times 100\) Percentage reacted = \(\frac{0.05051}{0.2} \times 100 \approx 25.26\% \) The percentage of calcium carbonate reacting to reach equilibrium by mass is 25.26%.

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Most popular questions from this chapter

At a particular temperature a \(2.00-\mathrm{L}\) flask at equilibrium contains \(2.80 \times 10^{-4}\) mole of \(\mathrm{N}_{2}, 2.50 \times 10^{-5}\) mole of \(\mathrm{O}_{2},\) and \(2.00 \times 10^{-2}\) mole of $\mathrm{N}_{2} \mathrm{O}\( . Calculate \)K$ at this temperature for the reaction $$2 \mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{N}_{2} \mathrm{O}(g)$$ If $\left[\mathrm{N}_{2}\right]=2.00 \times 10^{-4} M,\left[\mathrm{N}_{2} \mathrm{O}\right]=0.200 M,\( and \)\left[\mathrm{O}_{2}\right]=\( \)0.00245 M,$ does this represent a system at equilibrium?

Given \(K=3.50\) at \(45^{\circ} \mathrm{C}\) for the reaction $$\mathrm{A}(g)+\mathrm{B}(g) \rightleftharpoons \mathrm{C}(g)$$ and \(K=7.10\) at \(45^{\circ} \mathrm{C}\) for the reaction $$2 \mathrm{A}(g)+\mathrm{D}(g) \rightleftharpoons \mathrm{C}(g)$$ what is the value of \(K\) at the same temperature for the reaction $$\mathrm{C}(g)+\mathrm{D}(g) \rightleftharpoons 2 \mathrm{B}(g)$$ What is the value of \(K_{\mathrm{p}}\) at \(45^{\circ} \mathrm{C}\) for the reaction? Starting with 1.50 atm partial pressures of both \(\mathrm{C}\) and \(\mathrm{D},\) what is the mole fraction of \(\mathrm{B}\) once equilibrium is reached?

At a particular temperature, 8.1 moles of \(\mathrm{NO}_{2}\) gas are placed in a 3.0 -L container. Over time the \(\mathrm{NO}_{2}\) decomposes to \(\mathrm{NO}\) and \(\mathrm{O}_{2} :\) $$2 \mathrm{NO}_{2}(g) \rightleftharpoons 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g)$$ At equilibrium the concentration of \(\mathrm{NO}(g)\) was found to be 1.4 \(\mathrm{mol} / \mathrm{L}\) . Calculate the value of \(K\) for this reaction.

Nitric oxide and bromine at initial partial pressures of 98.4 and 41.3 torr, respectively, were allowed to react at \(300 .\) K. At equilibrium the total pressure was 110.5 torr. The reaction is $$2 \mathrm{NO}(g)+\mathrm{Br}_{2}(g) \rightleftharpoons 2 \mathrm{NOBr}(g)$$ a. Calculate the value of \(K_{\mathrm{p}}\) . b. What would be the partial pressures of all species if NO and \(\mathrm{Br}_{2},\) both at an initial partial pressure of \(0.30 \mathrm{atm},\) were allowed to come to equilibrium at this temperature?

Consider the following reaction: $$\mathrm{H}_{2} \mathrm{O}(g)+\mathrm{CO}(g) \rightleftharpoons \mathrm{H}_{2}(g)+\mathrm{CO}_{2}(g)$$ Amounts of \(\mathrm{H}_{2} \mathrm{O}, \mathrm{CO}, \mathrm{H}_{2},\) and \(\mathrm{CO}_{2}\) are put into a flask so that the composition corresponds to an equilibrium position. If the CO placed in the flask is labeled with radioactive \(^{14} \mathrm{C}\) will \(^{14} \mathrm{C}\) be found only in \(\mathrm{CO}\) molecules for an indefinite period of time? Explain.

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