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Consider the decomposition of the compound \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\) as follows: $$\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}(g) \rightleftharpoons \mathrm{C}_{2} \mathrm{H}_{6}(g)+3 \mathrm{CO}(g)$$ When a 5.63 -g sample of pure \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}(g)\) was sealed into an otherwise empty \(2.50-\mathrm{L}\) flask and heated to \(200 .^{\circ} \mathrm{C},\) the pres- sure in the flask gradually rose to 1.63 \(\mathrm{atm}\) and remained at that value. Calculate \(K\) for this reaction.

Short Answer

Expert verified
The equilibrium constant \(K\) for the given decomposition reaction of \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\) can be calculated by using the initial mass and volume of the system, the final pressure, and setting up an ICE table. Calculate initial moles, total moles at equilibrium, and changes in moles during the reaction to find equilibrium concentrations. Then, use these equilibrium concentrations to calculate the equilibrium constant \(K\).

Step by step solution

01

Find the initial moles

First, we need to find the initial moles of \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\) using the given mass and the molar mass of the compound. Molar mass of \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} = 5\times 12.01 + 6\times 1.01 + 3\times 16.00 = 114.11 \ \text{g/mol}\). Initial moles \((n_i)\) of \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} = \frac{5.63\ \text{g}}{114.11\ \text{g/mol}}\)
02

Setup the ICE table

Set up an ICE (initial, change, equilibrium) table to record the changes in moles of reactants and products during the reaction. Reaction: $$\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}(g) \rightleftharpoons \mathrm{C}_{2} \mathrm{H}_{6}(g)+3 \mathrm{CO}(g)$$ | | \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\) | \(\mathrm{C}_{2} \mathrm{H}_{6}\) | \(3\ \mathrm{CO}\) | |---------- |------------------------------------ |---------------------------- |-------------- | | Initial | \(n_i\) | 0 | 0 | | Change | \(-x\) | \(+x\) | \(+3x\) | | Equilibrium | \(n_i - x\) | \(x\) | \(3x\) |
03

Calculate final moles using the final pressure and ideal gas law

Using the final pressure \((P_f = 1.63\ \text{atm})\) and ideal gas law, we can find the total moles of gas at equilibrium and use it to calculate \(x\). Ideal Gas Law: \(PV=nRT\) Total moles of gas \((n_t)\) at equilibrium: $$n_t = \frac{PV}{RT} = \frac{(1.63\ \text{atm})(2.50\ \text{L})}{(0.0821\ \text{L.atm/mol.K})(293\ \text{K})}$$ As the total moles of gas at equilibrium are equal to the sum of moles of all the gases, we can write, $$n_t = n_{\text{C}_{5} \text{H}_{6} \text{O}_{3}} + n_{\text{C}_{2} \text{H}_{6}} + n_{\text{CO}} = (n_i - x) + x + 3x$$ Now we can substitute the known values and calculate \(x\).
04

Calculate the equilibrium concentrations

Once we have \(x\), we can find the equilibrium concentrations of \(\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}\), \(\mathrm{C}_{2} \mathrm{H}_{6}\), and \(\mathrm{CO}\) using the equilibrium moles and the given volume of the flask. Equilibrium concentration (\(\textit{conc}\)) for each species: \([\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}]_{eq} = \frac{n_{\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}}}{V} = \frac{n_i - x}{2.50\ \text{L}}\) \([\mathrm{C}_{2} \mathrm{H}_{6}]_{eq} = \frac{n_{\mathrm{C}_{2} \mathrm{H}_{6}}}{V} = \frac{x}{2.50\ \text{L}}\) \([\mathrm{CO}]_{eq} = \frac{n_{\mathrm{CO}}}{V} = \frac{3x}{2.50\ \text{L}}\)
05

Calculate the equilibrium constant

Finally, we can calculate the equilibrium constant using the known equilibrium concentrations and the balanced chemical equation: $$K = \frac{[\mathrm{C}_{2} \mathrm{H}_{6}]_{eq} [\mathrm{CO}]_{eq}^3}{[\mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3}]_{eq}}$$ Now, substitute the values for the equilibrium concentrations and calculate the value of \(K\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Equilibrium
Chemical equilibrium occurs when a chemical reaction reaches a state where the concentrations of reactants and products remain constant over time. This does not mean the reactions stop entirely but that the forward and reverse reactions occur at the same rate. Therefore, no net change in the amounts of substances occurs.

In the decomposition reaction of \,\( \mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} \) into \,\( \mathrm{C}_{2} \mathrm{H}_{6} \) and \,\( 3 \mathrm{CO} \), we reach equilibrium when the rate of forming \,\( \mathrm{C}_{2} \mathrm{H}_{6} \) and \,\( \mathrm{CO} \) equals the rate of their recombination to form \,\( \mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} \).

At equilibrium, the system can be described using the equilibrium constant \( K \), which is a ratio of the product concentrations to the reactant concentrations, each raised to the power of their stoichiometric coefficients. This value depends on temperature but not on the initial concentrations of reactants and products.
Ideal Gas Law
The Ideal Gas Law is a fundamental equation in chemistry, expressed as \,\( PV = nRT \). This relation connects the pressure \( P \), volume \( V \), and temperature \( T \) of a gas with the number of moles \( n \) and the ideal gas constant \( R = 0.0821 \ \text{L.atm/mol.K} \).

In the context of the decomposition reaction, this law helps us determine the total number of moles of gas present at equilibrium. By substituting given values of pressure, volume, and temperature of the system, we can calculate the total moles of gases formed.

This calculation is crucial as it allows us to figure out the extent of the reaction and ultimately the value of the equilibrium constant \( K \). Employing the Ideal Gas Law ensures that we understand how gas behaviors influence the equilibrium in gaseous reactions.
Decomposition Reactions
Decomposition reactions involve a single compound breaking down into two or more simpler substances. In the given exercise, the decomposition of \,\( \mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} \) results in the formation of \,\( \mathrm{C}_{2} \mathrm{H}_{6} \) and \,\( 3 \mathrm{CO} \).

Such reactions often require an external source of heat because breaking the bonds of the original compound requires energy. This specific decomposition reaction is initiated by heating the compound to \( 200. \ ^{\circ} \mathrm{C} \).

Decomposition reactions are significant in various scientific applications, including understanding stability profiles of compounds and determining energy requirements for product formation. This reaction type is fundamental in both academic studies and industrial processes.
ICE Table
The ICE table is a systematic method for keeping track of concentrations or moles of reactants and products in a chemical reaction over time. The acronym ICE stands for Initial, Change, and Equilibrium.

The ICE table begins with initial concentrations or moles before the reaction takes place. Then, based on the stoichiometry of the reaction, change values (usually represented with variables like \( x \)) are used to describe how much the concentrations of reactants decrease and products increase. Finally, the equilibrium row helps us compute their final concentrations or moles.

In the decomposition of \,\( \mathrm{C}_{5} \mathrm{H}_{6} \mathrm{O}_{3} \), the ICE table is instrumental to organize how the number of moles of each substance changes and reaches its equilibrium state. This setup allows for straightforward calculations of equilibrium concentrations, enabling the determination of the equilibrium constant \( K \).

By using the ICE table, one can systematically solve complex equilibrium problems with clarity and precision.

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Most popular questions from this chapter

Le Chatelier's principle is stated (Section 13.7\()\) as follows: "If a change is imposed on a system at equilibrium, the position of the equilibrium will shift in a direction that tends to reduce that change." The system \(\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons 2 \mathrm{NH}_{3}(g)\) is used as an example in which the addition of nitrogen gas at equilibrium results in a decrease in \(\mathrm{H}_{2}\) concentration and an increase in \(\mathrm{NH}_{3}\) concentration. In the experiment the volume is assumed to be constant. On the other hand, if \(\mathrm{N}_{2}\) is added to the reaction system in a container with a piston so that the pressure can be held constant, the amount of \(\mathrm{NH}_{3}\) actually could decrease and the concentration of \(\mathrm{H}_{2}\) would increase as equilibrium is reestablished. Explain how this can happen. Also, if you consider this same system at equilibrium, the addition of an inert gas, holding the pressure constant, does affect the equilibrium position. Explain why the addition of an inert gas to this system in a rigid container does not affect the equilibrium position.

The equilibrium constant is 0.0900 at \(25^{\circ} \mathrm{C}\) for the reaction $$\mathrm{H}_{2} \mathrm{O}(g)+\mathrm{Cl}_{2} \mathrm{O}(g) \rightleftharpoons 2 \mathrm{HOCl}(g)$$ For which of the following sets of conditions is the system at equilibrium? For those that are not at equilibrium, in which direction will the system shift? a. A 1.0 -L flask contains 1.0 mole of HOCl, 0.10 mole of \(\mathrm{Cl}_{2} \mathrm{O}\) , and 0.10 mole of \(\mathrm{H}_{2} \mathrm{O}\) . b. A 2.0 -L flask contains 0.084 mole of HOCl, 0.080 mole of \(\mathrm{Cl}_{2} \mathrm{O}\) , and 0.98 mole of \(\mathrm{H}_{2} \mathrm{O}\) . c. A 3.0 - flask contains 0.25 mole of HOCl, 0.0010 mole of \(\mathrm{Cl}_{2} \mathrm{O},\) and 0.56 mole of \(\mathrm{H}_{2} \mathrm{O}\) .

At \(900^{\circ} \mathrm{C}, K_{\mathrm{p}}=1.04\) for the reaction $$\mathrm{CaCO}_{3}(s) \rightleftharpoons \mathrm{CaO}(s)+\mathrm{CO}_{2}(g)$$ At a low temperature, dry ice (solid \(\mathrm{CO}_{2} ),\) calcium oxide, and calcium carbonate are introduced into a \(50.0-\mathrm{L}\) reaction chamber. The temperature is raised to \(900^{\circ} \mathrm{C},\) resulting in the dry ice converting to gaseous \(\mathrm{CO}_{2} .\) For the following mixtures, will the initial amount of calcium oxide increase, decrease, or remain the same as the system moves toward equilibrium at \(900^{\circ} \mathrm{C} ?\) a. \(655 \mathrm{g} \mathrm{CaCO}_{3}, 95.0 \mathrm{g}\) CaO, \(P_{\mathrm{CO}_{2}}=2.55 \mathrm{atm}\) b. \(780 \mathrm{g} \mathrm{CaCO}_{3}, 1.00 \mathrm{g} \mathrm{CaO}, P_{\mathrm{CO}_{2}}=1.04 \mathrm{atm}\) c. \(0.14 \mathrm{g} \mathrm{CaCO}_{3}, 5000 \mathrm{g} \mathrm{CaO}, P_{\mathrm{CO}_{2}}=1.04 \mathrm{atm}\) d. \(715 \mathrm{g} \mathrm{CaCO}_{3}, 813 \mathrm{g} \mathrm{CaO}, P_{\mathrm{CO}_{2}}=0.211 \mathrm{atm}\)

The value of the equilibrium constant \(K\) depends on which of the following (more than one answer may be correct)? a. the initial concentrations of the reactants b. the initial concentrations of the products c. the temperature of the system d. the nature of the reactants and products Explain.

At \(125^{\circ} \mathrm{C}, K_{\mathrm{p}}=0.25\) for the reaction $$2 \mathrm{NaHCO}_{3}(s) \rightleftharpoons \mathrm{Na}_{2} \mathrm{CO}_{3}(s)+\mathrm{CO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(g)$$ A \(1.00-\mathrm{L}\) flask containing 10.0 \(\mathrm{g} \mathrm{NaHCO}_{3}\) is evacuated and heated to \(125^{\circ} \mathrm{C} .\) a. Calculate the partial pressures of \(\mathrm{CO}_{2}\) and \(\mathrm{H}_{2} \mathrm{O}\) after equilibrium is established. b. Calculate the masses of \(\mathrm{NaHCO}_{3}\) and \(\mathrm{Na}_{2} \mathrm{CO}_{3}\) present at equilibrium. c. Calculate the minimum container volume necessary for all of the \(\mathrm{NaHCO}_{3}\) to decompose.

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