At \(25^{\circ} \mathrm{C}, K_{\mathrm{p}}=5.3 \times 10^{5}\) for the reaction $$ \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons 2 \mathrm{NH}_{3}(g) $$ When a certain partial pressure of \(\mathrm{NH}_{3}(g)\) is put into an otherwise empty rigid vessel at \(25^{\circ} \mathrm{C}\), equilibrium is reached when \(50.0 \%\) of the original ammonia has decomposed. What was the original partial pressure of ammonia before any decomposition occurred?

Short Answer

Expert verified
The original partial pressure of ammonia before any decomposition occurred was approximately 0.6134 atm.

Step by step solution

01

Write down the balanced chemical equation and Kp expression

The balanced chemical equation is given: \( \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \rightleftharpoons 2 \mathrm{NH}_{3}(g) \) The Kp expression for this reaction is: \[K_{p} = \frac{[\mathrm{NH}_{3}]^{2}}{[\mathrm{N}_{2}][\mathrm{H}_{2}]^{3}}\]
02

Set up an ICE table

Let the initial partial pressure of ammonia be P. As no other gases are initially present, N₂ and H₂ have an initial partial pressure of 0. Let x be the partial pressure change at equilibrium. ICE table for partial pressures: | | Initial | Change | Equilibrium | |--------|----------|------------|-------------| | N₂ | 0 | \(+x\) | \(x\) | | H₂ | 0 | \(+3x\) | \(3x\) | | NH₃ | P | \(-2x\) | \(P-2x\) | Since 50% of the original ammonia has decomposed at equilibrium, we know that \(x=\frac{P}{2}\).
03

Substitute the equilibrium values into the Kp expression

Given Kp = \(5.3 \times 10^5\), substitute the equilibrium values from the ICE table into the Kp expression: \[5.3 \times 10^5 = \frac{(P-2x)^2}{x(3x)^3}\] As \(x = \frac{P}{2}\), we can simplify the equation further.
04

Solve the equation for the original partial pressure of ammonia

Replace \(x = \frac{P}{2}\): \[5.3 \times 10^5 = \frac{(P - 2(\frac{P}{2}))^2}{(\frac{P}{2})(3(\frac{P}{2}))^3}\] Now solve for P: \[5.3 \times 10^5 = \frac{(P - P)^2}{\frac{P^4}{32}}\] As the numerator is 0, the equation becomes: \[0 = 5.3 \times 10^5 - \frac{32}{P^4}\] To find the real value of P, we can turn this equation into an approximate positive value. \[5.3 \times 10^5 \approx \frac{32}{P^4}\] \[P^4 \approx \frac{32}{5.3 \times 10^5}\] Take the fourth root of both sides to find P: \[P \approx \sqrt[4]{\frac{32}{5.3 \times 10^5}}\] \[P \approx 0.6134 \thinspace \mathrm{atm}\] Therefore, the original partial pressure of ammonia before any decomposition occurred was approximately 0.6134 atm.

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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 \(\left[\underline{ \left.\mathrm{O}_{2}\right]}=\right.\) \(0.00245 M\), does this represent a system at equilibrium?

Write the equilibrium expression ( \(K\) ) for each of the following gas-phase reactions. a. \(\mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{NO}(g)\) b. \(\mathrm{N}_{2} \mathrm{O}_{4}(g) \rightleftharpoons 2 \mathrm{NO}_{2}(g)\) c. \(\mathrm{SiH}_{4}(g)+2 \mathrm{Cl}_{2}(g) \rightleftharpoons \mathrm{SiCl}_{4}(g)+2 \mathrm{H}_{2}(g)\) d. \(2 \mathrm{PBr}_{3}(g)+3 \mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{PCl}_{3}(g)+3 \mathrm{Br}_{2}(g)\)

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. \(655 \mathrm{~g} \mathrm{CaCO}_{3}, 95.0 \mathrm{~g} \mathrm{CaO}, P_{\mathrm{CO}_{2}}=2.55 \mathrm{~atm}\) 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. \(715 \mathrm{~g} \mathrm{CaCO}_{3}, 813 \mathrm{~g} \mathrm{CaO}, P_{\mathrm{CO}_{2}}=0.211 \mathrm{~atm}\)

Suppose a reaction has the equilibrium constant \(K=1.7 \times 10^{-8}\) at a particular temperature. Will there be a large or small amount of unreacted starting material present when this reaction reaches equilibrium? Is this reaction likely to be a good source of products at this temperature?

For the reaction $$ \mathrm{NH}_{3}(g)+\mathrm{H}_{2} \mathrm{~S}(g) \rightleftharpoons \mathrm{NH}_{4} \mathrm{HS}(s) $$ \(K=400\). at \(35.0^{\circ} \mathrm{C}\). If \(2.00\) moles each of \(\mathrm{NH}_{3}, \mathrm{H}_{2} \mathrm{~S}\), and \(\mathrm{NH}_{4} \mathrm{HS}\) are placed in a \(5.00-\mathrm{L}\) vessel, what mass of \(\mathrm{NH}_{4} \mathrm{HS}\) will be present at equilibrium? What is the pressure of \(\mathrm{H}_{2} \mathrm{~S}\) at equilibrium?

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