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Chemical Equilibrium question

2016 · Shift 2 · Q6
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  5. /2016 · Shift 2 · Q6

Chemical Equilibrium question

2016 · Shift 2 · Q6

JEE AdvancedChemistryChemical EquilibriumMCQ+3 / −1
Paragraph Thermal decomposition of gaseous X2X_2X2​ to gaseous X at 298 K takes place according to the following equations: X2X_2X2​ (g) ⇋\leftrightharpoons⇋ 2X (g) The standard reaction Gibbs energy, ΔrGo\Delta _rG^oΔr​Go, of this reaction is positive. At the start of the reaction, there is one mole of X2X_2X2​ and no X. As the reaction proceeds, the number of moles of X formed is given by β\betaβ. Thus, βequilibrium\beta _{equilibrium}βequilibrium​ is the number of moles of X formed at equilibrium. The reaction is carried out at a constant total pressure of 2 bar. Consider the gases to behave ideally. (Given R = 0.083 L bar K-1 mol-1) Question The equilibrium constant Kp for this reaction at 298 K, in terms of βequilibrium\beta _{equilibrium}βequilibrium​, is
  1. A
    8βequilibrium22−βequilibrium{{8\beta _{equilibrium}^2} \over {2 - {\beta _{equilibrium}}}}2−βequilibrium​8βequilibrium2​​
  2. B
    8βequilibrium24−βequilibrium2{{8\beta _{equilibrium}^2} \over {4 - {\beta _{equilibrium}^2}}}4−βequilibrium2​8βequilibrium2​​
  3. C
    4βequilibrium22−βequilibrium{{4\beta _{equilibrium}^2} \over {2 - {\beta _{equilibrium}}}}2−βequilibrium​4βequilibrium2​​
  4. D
    4βequilibrium24−βequilibrium2{{4\beta _{equilibrium}^2} \over {4 - {\beta _{equilibrium}^2}}}4−βequilibrium2​4βequilibrium2​​
View written solutionFree

Correct answer: B

  1. Set up the reaction and mole balance

The reaction is X2(g)⇌2X(g)X_2(g) \rightleftharpoons 2X(g)X2​(g)⇌2X(g)

Initially:

  • moles of X2=1X_2 = 1X2​=1
  • moles of X=0X = 0X=0

Let β\betaβ be the number of moles of XXX formed at equilibrium.

Since 1 mole of X2X_2X2​ produces 2 moles of XXX, the moles of X2X_2X2​ decomposed are: β2\frac{\beta}{2}2β​

So at equilibrium: nX2=1−β2,nX=βn_{X_2}=1-\frac{\beta}{2}, \qquad n_X=\betanX2​​=1−2β​,nX​=β

Total moles at equilibrium: ntot=1−β2+β=1+β2n_{\text{tot}}=1-\frac{\beta}{2}+\beta=1+\frac{\beta}{2}ntot​=1−2β​+β=1+2β​


  1. Write mole fractions

yX2=1−β/21+β/2y_{X_2}=\frac{1-\beta/2}{1+\beta/2}yX2​​=1+β/21−β/2​

yX=β1+β/2y_X=\frac{\beta}{1+\beta/2}yX​=1+β/2β​

Given total pressure, P=2 barP=2\,\text{bar}P=2bar

Hence partial pressures are: pX2=yX2P=1−β/21+β/2⋅2p_{X_2}=y_{X_2}P=\frac{1-\beta/2}{1+\beta/2}\cdot 2pX2​​=yX2​​P=1+β/21−β/2​⋅2

pX=yXP=β1+β/2⋅2p_X=y_XP=\frac{\beta}{1+\beta/2}\cdot 2pX​=yX​P=1+β/2β​⋅2


  1. Expression for KpK_pKp​

For the reaction X2(g)⇌2X(g)X_2(g) \rightleftharpoons 2X(g)X2​(g)⇌2X(g)

Kp=(pX)2pX2K_p=\frac{(p_X)^2}{p_{X_2}}Kp​=pX2​​(pX​)2​

Substitute the above expressions: Kp=(2β1+β/2)2(2(1−β/2)1+β/2)K_p=\frac{\left(\dfrac{2\beta}{1+\beta/2}\right)^2}{\left(\dfrac{2(1-\beta/2)}{1+\beta/2}\right)}Kp​=(1+β/22(1−β/2)​)(1+β/22β​)2​

Now simplify: Kp=4β2(1+β/2)22(1−β/2)1+β/2K_p=\frac{\dfrac{4\beta^2}{(1+\beta/2)^2}}{\dfrac{2(1-\beta/2)}{1+\beta/2}}Kp​=1+β/22(1−β/2)​(1+β/2)24β2​​

Kp=4β2(1+β/2)2⋅1+β/22(1−β/2)K_p=\frac{4\beta^2}{(1+\beta/2)^2}\cdot \frac{1+\beta/2}{2(1-\beta/2)}Kp​=(1+β/2)24β2​⋅2(1−β/2)1+β/2​

Kp=2β2(1+β/2)(1−β/2)K_p=\frac{2\beta^2}{(1+\beta/2)(1-\beta/2)}Kp​=(1+β/2)(1−β/2)2β2​

Use (1+β/2)(1−β/2)=1−β24(1+\beta/2)(1-\beta/2)=1-\frac{\beta^2}{4}(1+β/2)(1−β/2)=1−4β2​

So, Kp=2β21−β2/4K_p=\frac{2\beta^2}{1-\beta^2/4}Kp​=1−β2/42β2​

Multiply numerator and denominator by 4: Kp=8β24−β2K_p=\frac{8\beta^2}{4-\beta^2}Kp​=4−β28β2​

At equilibrium, β=βequilibrium\beta=\beta_{\text{equilibrium}}β=βequilibrium​, hence Kp=8βequilibrium24−βequilibrium2K_p=\frac{8\beta_{\text{equilibrium}}^2}{4-\beta_{\text{equilibrium}}^2}Kp​=4−βequilibrium2​8βequilibrium2​​


  1. Match with options

This corresponds to: B\boxed{\text{B}}B​


  1. Comparison with stored correct answer

Stored correct answer: B

Derived answer: B

So, the derived answer agrees with the stored correct answer.

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