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Ionic Equilibrium question

2024 · 6 Apr · Shift 1 · Q23
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  5. /2024 · 6 Apr · Shift 1 · Q23

Ionic Equilibrium question

2024 · 6 Apr · Shift 1 · Q23

JEE MainChemistryIonic EquilibriumNumerical+4 / −1
Consider the dissociation of the weak acid HX as given below HX(aq)⇌H+(aq)+X−(aq),Ka=1.2×10−5\mathrm{HX}(\mathrm{aq}) \rightleftharpoons \mathrm{H}^{+}(\mathrm{aq})+\mathrm{X}^{-}(\mathrm{aq}), \mathrm{Ka}=1.2 \times 10^{-5}HX(aq)⇌H+(aq)+X−(aq),Ka=1.2×10−5[Ka\mathrm{K}_{\mathrm{a}}Ka​: dissociation constant] The osmotic pressure of 0.03M0.03 \mathrm{M}0.03M aqueous solution of HX\mathrm{HX}HX at 300 K300 \mathrm{~K}300 K is ‾\underline{\hspace{2cm}}​×10−2\times 10^{-2}×10−2 bar (nearest integer). [Given : R=0.083 L bar mol−1 K−1\mathrm{R}=0.083 \mathrm{~L} \mathrm{~bar} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}R=0.083 L bar mol−1 K−1]
Numerical answer
View written solutionFree

Correct answer: 76

  1. Given data

    HX(aq)⇌H+(aq)+X−(aq),Ka=1.2×10−5\mathrm{HX}(aq) \rightleftharpoons \mathrm{H^+}(aq) + \mathrm{X^-}(aq), \qquad K_a = 1.2\times 10^{-5}HX(aq)⇌H+(aq)+X−(aq),Ka​=1.2×10−5

    Concentration of acid: C=0.03 MC = 0.03\,\text{M}C=0.03M

    Temperature: T=300 KT = 300\,\text{K}T=300K

    Gas constant: R=0.083 L bar mol−1K−1R = 0.083\,\text{L bar mol}^{-1}\text{K}^{-1}R=0.083L bar mol−1K−1

  2. Find degree of dissociation

    Let degree of dissociation be α\alphaα.

    Initial and equilibrium concentrations:

    & \mathrm{HX} & \mathrm{H^+} & \mathrm{X^-} \\ \hline \text{Initial} & C & 0 & 0 \\ \text{Change} & -C\alpha & +C\alpha & +C\alpha \\ \text{Equilibrium} & C(1-\alpha) & C\alpha & C\alpha \end{array}$$ Therefore, $$K_a = \frac{[\mathrm{H^+}][\mathrm{X^-}]}{[\mathrm{HX}]} = \frac{(C\alpha)(C\alpha)}{C(1-\alpha)} = \frac{C\alpha^2}{1-\alpha}$$ Since HX is a weak acid, $\alpha$ is small, so $1-\alpha \approx 1$. Hence, $$K_a \approx C\alpha^2$$ $$\alpha = \sqrt{\frac{K_a}{C}} = \sqrt{\frac{1.2\times 10^{-5}}{0.03}}$$ $$\alpha = \sqrt{4\times 10^{-4}} = 2\times 10^{-2} = 0.02$$
  3. Van't Hoff factor

    For HX→H++X−\mathrm{HX} \to \mathrm{H^+} + \mathrm{X^-}HX→H++X− one particle gives 2 particles on dissociation.

    Therefore, i=1+α=1+0.02=1.02i = 1 + \alpha = 1 + 0.02 = 1.02i=1+α=1+0.02=1.02

  4. Osmotic pressure formula

    π=iCRT\pi = iCRTπ=iCRT

    Substitute the values: π=(1.02)(0.03)(0.083)(300)\pi = (1.02)(0.03)(0.083)(300)π=(1.02)(0.03)(0.083)(300)

    First, 0.083×300=24.90.083\times 300 = 24.90.083×300=24.9

    Then, 0.03×24.9=0.7470.03\times 24.9 = 0.7470.03×24.9=0.747

    Finally, π=1.02×0.747=0.76194 bar\pi = 1.02\times 0.747 = 0.76194\,\text{bar}π=1.02×0.747=0.76194bar

  5. Express in the asked form

    We need π=‾×10−2 bar\pi = \underline{\hspace{1cm}} \times 10^{-2}\,\text{bar}π=​×10−2bar

    0.76194 bar=76.194×10−2 bar0.76194\,\text{bar} = 76.194\times 10^{-2}\,\text{bar}0.76194bar=76.194×10−2bar

    Nearest integer =76= 76=76.

  6. Final answer

    76\boxed{76}76​

  7. Comparison with stored answer

    Stored correct answer = 767676.

    My derived answer matches the stored answer.

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