The total pressure observed by mixing two liquids A and B is 350 , mm Hg when their mole fractions are 0.7 and 0.3 respectively The total pressure becomes 410 ,mm ,Hg if the mole fractions are changed to 0.2 and 0.8 respectively for A and B The vapour pressure of pure A is _________mm ,Hg (Nearest integer) Consider the liquids and solutions behave ideally.
Use Raoult's law: \(P_{\text{total}} = P_A^0 X_A + P_B^0 X_B\) for ideal solutions. Solve simultaneous equations for unknown vapour pressures.
To solve this problem, we apply Raoult's law, which is valid for ideal solutions. According to Raoult's law, the total vapor pressure \(P\) of a solution can be computed as:
\(P = x_A \cdot P_A^0 + x_B \cdot P_B^0\) where:
We have the following two equations from the problem:
1. For \(x_A = 0.7\) and \(x_B = 0.3\), total pressure \(P = 350\) mm Hg:
\(0.7 \cdot P_A^0 + 0.3 \cdot P_B^0 = 350\)
2. For \(x_A = 0.2\) and \(x_B = 0.8\), total pressure \(P = 410\) mm Hg:
\(0.2 \cdot P_A^0 + 0.8 \cdot P_B^0 = 410\)
We solve these simultaneous equations to find \(P_A^0\) and \(P_B^0\).
Multiply equation (1) by 4 and equation (2) by 7 to eliminate \(P_B^0\):
Equation (1):
\((4 \cdot 0.7) \cdot P_A^0 + (4 \cdot 0.3) \cdot P_B^0 = 4 \cdot 350\)
\(2.8 \cdot P_A^0 + 1.2 \cdot P_B^0 = 1400\)
Equation (2):
\((7 \cdot 0.2) \cdot P_A^0 + (7 \cdot 0.8) \cdot P_B^0 = 7 \cdot 410\)
\(1.4 \cdot P_A^0 + 5.6 \cdot P_B^0 = 2870\)
Subtract equation (1) from equation (2):
\((1.4 - 2.8) \cdot P_A^0 + (5.6 - 1.2) \cdot P_B^0 = 2870 - 1400\)
\(-1.4 \cdot P_A^0 + 4.4 \cdot P_B^0 = 1470\)
Re-arranging:
\(4.4 \cdot P_B^0 = 1.4 \cdot P_A^0 + 1470\)
\(P_B^0 = \frac{1.4 \cdot P_A^0 + 1470}{4.4}\)
Substitute \(P_B^0\) back into equation (1):
\(0.7 \cdot P_A^0 + 0.3 \cdot \left(\frac{1.4 \cdot P_A^0 + 1470}{4.4}\right) = 350\)
Simplifying:
\(0.7 \cdot P_A^0 + \frac{0.42 \cdot P_A^0 + 441}{4.4} = 350\)
\(0.7 \cdot P_A^0 + \frac{0.42 \cdot P_A^0 + 441}{4.4} = 350\)
\(0.7 \cdot P_A^0 \cdot 4.4 + 0.42 \cdot P_A^0 + 441 = 1540\)
\(3.08 \cdot P_A^0 + 0.42 \cdot P_A^0 = 1540 - 441\)
\(3.5 \cdot P_A^0 = 1099\)
\(P_A^0 = \frac{1099}{3.5}\)
\(P_A^0 ≈ 314\) mm Hg.
The calculated vapor pressure of pure A, \(314\) mm Hg, satisfies the expected range of 314,314. Therefore, the vapor pressure of pure A is \(314\) mm Hg.
The freezing point depression constant (\( K_f \)) for water is \( 1.86 \, {°C·kg/mol} \). If 0.5 moles of a non-volatile solute is dissolved in 1 kg of water, calculate the freezing point depression.