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Question: Ammonia gas at \(76cm\,Hg\) pressure was connected to a manometer. After sparking in the flask, ammo...

Ammonia gas at 76cmHg76cm\,Hg pressure was connected to a manometer. After sparking in the flask, ammonia is partially dissociated as follows:
2NH3(g)N2(g)+3H2(g)2N{H_3}\left( g \right) \rightleftharpoons {N_2}\left( g \right) + 3{H_2}\left( g \right)
The level in the mercury column of the manometer was found to show a difference of 18cm18cm. What is the partial pressure of H2(g){H_2}\left( g \right)at equilibrium?
(A) 18cmHg18cm\,Hg
(B) 9cmHg9cm\,Hg
(C) 27cmHg27cm\,Hg
(D) 24cmHg24cm\,Hg

Explanation

Solution

According to the ideal gas law, partial pressure is inversely proportional to volume. It is also directly proportional to moles and temperature.

Complete step by step answer:
According to the question, ammonia is partially dissociated to nitrogen gas and hydrogen gas as follows:
2NH3(g)N2(g)+3H2(g)2N{H_3}\left( g \right) \rightleftharpoons {N_2}\left( g \right) + 3{H_2}\left( g \right)
It is given that ammonia NH3N{H_3} is at 76cmHg76cm\,\,Hg pressure
Therefore, we can consider 76cmHg76cm\,\,Hg as the initial pressure.
Initial, NH3(g)76cmHgN2(g)0+3H2(g)0\mathop {N{H_3}\left( g \right)}\limits_{76cm\,\,Hg} \rightleftharpoons \mathop {{N_2}\left( g \right)}\limits_0 + \mathop {3{H_2}\left( g \right)}\limits_0
Let at time =t = tequilibrium is obtained and the dissociation (let) be xx
At time = t$$$$\begin{array}{*{20}{c}} {76 - 2x}& &{3x} \end{array}
(Equilibrium)
Thus, we have written taking in view the stoichiometric coefficients.
The total pressure after dissociation =762x+x+3x=76+2x = 76 - 2x + x + 3x = 76 + 2x
So, the increase in pressure =762x76=2x = 76 - 2x - 76 = 2x
Increase in pressure = 18cmHg18cm\,Hg
(as given in the question)
2x=182x = 18
x=9cmHgx = 9cm\,Hg
We know that, the partial pressure of H2(g){H_2}\left( g \right)is 3x3x so the answer is 3×9=27cm3 \times 9 = 27cm

So, the correct answer is “Option C”.

Additional Information:
The total pressure of a mixture of gases can be defined as the sum of pressures of each individual gas
PTotal = P1+P2+P3+P4......P\,{\text{Total = }}{{\text{P}}_1} + {{\text{P}}_2} + {{\text{P}}_3} + {{\text{P}}_4}......

Note:
The partial pressure of an individual gas is equal to the total pressure multiplied by mole fraction of that gas.
Partial pressure of Gas A = Total pressure ×mole fraction of Gas A{\text{Partial pressure of Gas A = Total pressure }} \times {\text{mole fraction of Gas A}}
PA = PTXA{{\text{P}}_{\text{A}}}{\text{ = }}{{\text{P}}_{\text{T}}}{{\text{X}}_{\text{A}}}