The dissociation of HX is represented as:
\[\text{HX} \rightleftharpoons \text{H}^+ + \text{X}^-\]
Initial concentration of HX: 0.03 M
At equilibrium:
\[[\text{HX}] = 0.03 - x, \quad [\text{H}^+] = x, \quad [\text{X}^-] = x\]
Using the dissociation constant $K_a$:
\[K_a = \frac{x^2}{0.03 - x}\]
For $K_a = 1.2 \times 10^{-5}$ and $0.03 - x \approx 0.03$ (since $K_a$ is very small):
\[1.2 \times 10^{-5} = \frac{x^2}{0.03}\]
\[x^2 = 1.2 \times 10^{-5} \times 0.03 = 3.6 \times 10^{-7}\]
\[x = \sqrt{3.6 \times 10^{-7}} = 6 \times 10^{-4}\]
Total solute concentration:
\[C_{\text{total}} = [\text{HX}] + [\text{H}^+] + [\text{X}^-] = 0.03 - x + x + x = 0.03 + x\]
\[C_{\text{total}} = 0.03 + 6 \times 10^{-4} = 0.0306 \, \text{M}\]
Osmotic pressure $\Pi$ is calculated using:
\[\Pi = C_{\text{total}}RT\]
\[\Pi = (0.0306) \times (0.083) \times (300)\]
\[\Pi = 76.19 \, \text{bar}\]
Nearest integer:
\[\Pi = 76 \times 10^{-2} \, \text{bar}\]
If \(A_2B \;\text{is} \;30\%\) ionised in an aqueous solution, then the value of van’t Hoff factor \( i \) is:
1.24 g of \(AX_2\) (molar mass 124 g mol\(^{-1}\)) is dissolved in 1 kg of water to form a solution with boiling point of 100.105°C, while 2.54 g of AY_2 (molar mass 250 g mol\(^{-1}\)) in 2 kg of water constitutes a solution with a boiling point of 100.026°C. \(Kb(H)_2\)\(\text(O)\) = 0.52 K kg mol\(^{-1}\). Which of the following is correct?