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Grade 12th passPhysical Chemistry

I have 2 doubts:
1>
100cc of 1.5% solution of urea is found to have an osmotic pressure of 6atm and 100cc of 3.42% solution of cane sugar is found to have an osmotic pressure of 2.4atm. If two solutions are mixed, the osmotic pressure of the resulting mix is?
a 8.4 atm b 4.2 atm c 16.8 atm d 2.1 atm
2>
When 25g of a non-volatile solute is dissolved in 100g of water, the vapour pressure is lowered by 2.25 x 10-1 mm. If the vapour pressure of water at 20oC is 17.5mm, what is the molecular weight of the solute?
a)206 b)302 c)350 d)276

Profile image of Ashmeet Lamba
9 Years agoGrade 12th pass
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1 Answer

Profile image of Askiitians Tutor Team
ApprovedApproved Tutor Answer1 Year ago

Let’s tackle your questions one at a time, starting with the first one about osmotic pressure. To find the osmotic pressure of the resulting mixture when two solutions are combined, we can use the formula for osmotic pressure, which is given by the equation:

Understanding Osmotic Pressure

The osmotic pressure (π) of a solution can be calculated using the formula:

π = iCRT

Where:

  • i = van 't Hoff factor (number of particles the solute dissociates into)
  • C = molarity of the solution
  • R = ideal gas constant (0.0821 L·atm/(K·mol))
  • T = temperature in Kelvin

In your case, we have two solutions:

  • Solution 1: 100 cc of 1.5% urea solution with an osmotic pressure of 6 atm
  • Solution 2: 100 cc of 3.42% cane sugar solution with an osmotic pressure of 2.4 atm

Calculating the Total Osmotic Pressure

When mixing two solutions, the total osmotic pressure can be found by simply adding the individual osmotic pressures of the two solutions, assuming they behave ideally and do not interact significantly. Thus:

π_total = π_urea + π_sugar

Substituting the values:

π_total = 6 atm + 2.4 atm = 8.4 atm

So, the answer to your first question is a) 8.4 atm.

Determining Molecular Weight of a Solute

Now, let’s move on to your second question regarding the molecular weight of a non-volatile solute. We can use Raoult's Law, which states that the vapor pressure of a solvent is directly proportional to the mole fraction of the solvent in the solution.

The formula for the change in vapor pressure (ΔP) is:

ΔP = P° - P

Where:

  • = vapor pressure of pure solvent
  • P = vapor pressure of the solution

Given:

  • ΔP = 2.25 x 10-1 mm
  • P° = 17.5 mm

First, we can find the vapor pressure of the solution:

P = P° - ΔP = 17.5 mm - 0.225 mm = 17.275 mm

Calculating Mole Fraction and Molecular Weight

Next, we can find the mole fraction of the solute (X_solute) using the formula:

ΔP/P° = X_solute

Substituting the values:

2.25 x 10-1 mm / 17.5 mm = X_solute

X_solute = 0.012857

Now, we know that:

X_solute = n_solute / (n_solute + n_solvent)

Where:

  • n_solute = moles of solute
  • n_solvent = moles of solvent (water)

For 100 g of water, the number of moles of water (molar mass = 18 g/mol) is:

n_solvent = 100 g / 18 g/mol = 5.56 mol

Let’s denote the molar mass of the solute as M. The number of moles of solute can be expressed as:

n_solute = mass of solute / M = 25 g / M

Substituting into the mole fraction equation:

0.012857 = (25/M) / (25/M + 5.56)

Cross-multiplying and simplifying gives:

0.012857(25 + 5.56M) = 25

0.321425 + 0.071428M = 25

0.071428M = 24.678575

M = 24.678575 / 0.071428 ≈ 346.5 g/mol

After rounding, the closest answer from your options is c) 350.

In summary, the answers to your questions are:

  • First question: a) 8.4 atm
  • Second question: c) 350