A non-volatile solute, urea ($CO(NH_2)_2$, molar mass $60 \ g/mol$), is dissolved in $180 \ g$ of water ($H_2O$, molar mass $18 \ g/mol$). If the vapor pressure of pure water at a certain temperature is $50 \ mmHg$, what is the vapor pressure of the solution when $18 \ g$ of urea is added?
$48.54 \ mmHg$
This problem involves calculating the vapor pressure of a solution containing a non-volatile solute (urea) dissolved in a solvent (water). We can solve this using Raoult's Law, which describes the relationship between the mole fraction of the solvent and the vapor pressure of the solution.
We are given:
The core principle here is Raoult's Law for solutions with non-volatile solutes. It states that the vapor pressure of the solution is equal to the mole fraction of the solvent multiplied by the vapor pressure of the pure solvent.
The formula is:
$P_{solution} = X_{solvent} \times P^0_{solvent}$
Where:
To find the mole fraction of the solvent ($X_{solvent}$), we need the moles of the solvent ($n_{solvent}$) and the moles of the solute ($n_{solute}$):
$X_{solvent} = \frac{n_{solvent}}{n_{solvent} + n_{solute}}$
The number of moles ($n$) is calculated as:
$n = \frac{\text{mass}}{\text{molar mass}}$
Using the given mass and molar mass of urea:
$n_{urea} = \frac{18 \ g}{60 \ g/mol} = 0.3 \ mol$
Using the given mass and molar mass of water:
$n_{water} = \frac{180 \ g}{18 \ g/mol} = 10 \ mol$
The total number of moles in the solution is the sum of the moles of water and urea:
$n_{total} = n_{water} + n_{urea} = 10 \ mol + 0.3 \ mol = 10.3 \ mol$
Now, we find the mole fraction of water:
$X_{water} = \frac{n_{water}}{n_{total}} = \frac{10 \ mol}{10.3 \ mol}$
$X_{water} \approx 0.97087$
Apply Raoult's Law using the calculated mole fraction of water and the given vapor pressure of pure water:
$P_{solution} = X_{water} \times P^0_{water}$
$P_{solution} = \frac{10}{10.3} \times 50 \ mmHg$
$P_{solution} \approx 0.97087 \times 50 \ mmHg$
$P_{solution} \approx 48.5435 \ mmHg$
Rounding the result to two decimal places, the vapor pressure of the solution is approximately $48.54 \ mmHg$. This value is lower than the vapor pressure of pure water, as expected when a non-volatile solute is added.
Detailed breakdown of the calculation:
| Component | Mass (g) | Molar Mass (g/mol) | Moles (mol) |
|---|---|---|---|
| Urea ($CO(NH_2)_2$) | $18$ | $60$ | $18 / 60 = 0.3$ |
| Water ($H_2O$) | $180$ | $18$ | $180 / 18 = 10$ |
Total Moles = Moles of Water + Moles of Urea = $10 \ mol + 0.3 \ mol = 10.3 \ mol$
Mole Fraction of Water ($X_{water}$) = $\frac{\text{Moles of Water}}{\text{Total Moles}} = \frac{10}{10.3}$
Vapor Pressure of Solution ($P_{solution}$) = $X_{water} \times P^0_{water}$ = $\frac{10}{10.3} \times 50 \ mmHg \approx 48.54 \ mmHg$
What will happen to the boiling point of water when a little common salt is added to water and then heated?
Which Statement is correct ?
The pH value of 1 × 10 -8 (M) HCl is:
Tyndall effect is not observed in:
Calculate the mass in grams of $0.25$ moles of calcium phosphate, $Ca_3(PO_4)_2$.
Use the following approximate atomic masses:
$Ca = 40.08 \text{ g/mol}$
$P = 30.97 \text{ g/mol}$
$O = 16.00 \text{ g/mol}$