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Solutions question

2024 · 4 Apr · Shift 1 · Q21
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Solutions question

2024 · 4 Apr · Shift 1 · Q21

JEE MainChemistrySolutionsNumerical+4 / −1
2.5 g2.5 \mathrm{~g}2.5 g of a non-volatile, non-electrolyte is dissolved in 100 g100 \mathrm{~g}100 g of water at 25∘C25^{\circ} \mathrm{C}25∘C. The solution showed a boiling point elevation by 2∘C2^{\circ} \mathrm{C}2∘C. Assuming the solute concentration is negligible with respect to the solvent concentration, the vapor pressure of the resulting aqueous solution is ‾mm\underline{\hspace{2cm}}\mathrm{mm}​mm of Hg\mathrm{Hg}Hg(nearest integer) [Given : Molal boiling point elevation constant of water (Kb)=0.52 K.kgmol−1\left(\mathrm{K}_{\mathrm{b}}\right)=0.52 \mathrm{~K} . \mathrm{kg} \mathrm{mol}^{-1}(Kb​)=0.52 K.kgmol−1, 1 atm1 \mathrm{~atm}1 atm pressure =760 mm=760 \mathrm{~mm}=760 mm of Hg\mathrm{Hg}Hg, molar mass of water =18 g mol−1]=18 \mathrm{~g} \mathrm{~mol}^{-1}]=18 g mol−1]
Numerical answer
View written solutionFree

Correct answer: 707

  1. Use boiling point elevation to find molality

For a non-volatile, non-electrolyte:

ΔTb=Kbm\Delta T_b = K_b mΔTb​=Kb​m

Given:

ΔTb=2 K,Kb=0.52 K kg mol−1\Delta T_b = 2\,\text{K}, \qquad K_b = 0.52\,\text{K kg mol}^{-1}ΔTb​=2K,Kb​=0.52K kg mol−1

So,

m=ΔTbKb=20.52=3.846 mol kg−1m = \frac{\Delta T_b}{K_b} = \frac{2}{0.52} = 3.846\,\text{mol kg}^{-1}m=Kb​ΔTb​​=0.522​=3.846mol kg−1

  1. Calculate moles of solute in 100 g water

Mass of water:

100 g=0.100 kg100\,\text{g} = 0.100\,\text{kg}100g=0.100kg

Hence moles of solute:

n2=m×0.100=3.846×0.100=0.3846 moln_2 = m \times 0.100 = 3.846 \times 0.100 = 0.3846\,\text{mol}n2​=m×0.100=3.846×0.100=0.3846mol

  1. Calculate moles of water

n1=10018=5.556 moln_1 = \frac{100}{18} = 5.556\,\text{mol}n1​=18100​=5.556mol

  1. Find mole fraction of solvent

For a non-volatile solute, by Raoult’s law:

P=X1P0P = X_1 P^0P=X1​P0

Since the question says solute concentration is negligible with respect to solvent concentration, we use the approximation:

X1≈n1n1+n2X_1 \approx \frac{n_1}{n_1+n_2}X1​≈n1​+n2​n1​​

Now,

X1=5.5565.556+0.3846=5.5565.9406≈0.9353X_1 = \frac{5.556}{5.556+0.3846} = \frac{5.556}{5.9406} \approx 0.9353X1​=5.556+0.38465.556​=5.94065.556​≈0.9353

  1. Vapour pressure of solution

Taking vapour pressure of pure water as 1 atm=760 mm Hg1\,\text{atm} = 760\,\text{mm Hg}1atm=760mm Hg,

P=0.9353×760≈710.8 mm HgP = 0.9353 \times 760 \approx 710.8\,\text{mm Hg}P=0.9353×760≈710.8mm Hg

Nearest integer:

P≈711 mm HgP \approx 711\,\text{mm Hg}P≈711mm Hg

  1. Compare with stored answer

Derived answer is 711 mm Hg, whereas stored correct answer is 707 mm Hg.

The likely reason for the discrepancy is that the exact data used here lead to about 711 mm Hg711\,\text{mm Hg}711mm Hg. The value 707707707 does not follow from the standard application of boiling point elevation and Raoult’s law with the given constants.

If one uses the approximation for dilute solution directly:

ΔPP0=X2≈n2n1=0.38465.556≈0.0692\frac{\Delta P}{P^0} = X_2 \approx \frac{n_2}{n_1} = \frac{0.3846}{5.556} \approx 0.0692P0ΔP​=X2​≈n1​n2​​=5.5560.3846​≈0.0692

Then,

P=760(1−0.0692)≈707.4 mm HgP = 760(1-0.0692) \approx 707.4\,\text{mm Hg}P=760(1−0.0692)≈707.4mm Hg

which gives 707 mm Hg.

Since the problem explicitly says solute concentration is negligible compared to solvent concentration, this dilute-solution approximation is intended. Hence the exam-style expected answer is 707 mm Hg.

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