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.
Given:
The formula for freezing point depression is given by: \[ \Delta T_f = K_f \times m \] where: - \( \Delta T_f \) is the freezing point depression, - \( K_f \) is the freezing point depression constant, - \( m \) is the molality of the solution.
Molality is calculated using: \[ m = \frac{\text{moles of solute}}{\text{mass of solvent in kg}} \] Substituting the given values: \[ m = \frac{0.5 \, \text{mol}}{1 \, \text{kg}} = 0.5 \, \text{mol/kg} \]
Now, using the freezing point depression formula: \[ \Delta T_f = 1.86 \, \text{°C} \cdot \text{kg/mol} \times 0.5 \, \text{mol/kg} \] \[ \Delta T_f = 0.93 \, \text{°C} \]
The freezing point depression is \( \boxed{0.93 \, \text{°C}} \).
According to the generally accepted definition of the ideal solution there are equal interaction forces acting between molecules belonging to the same or different species. (This is equivalent to the statement that the activity of the components equals the concentration.) Strictly speaking, this concept is valid in ecological systems (isotopic mixtures of an element, hydrocarbons mixtures, etc.). It is still usual to talk about ideal solutions as limiting cases in reality since very dilute solutions behave ideally with respect to the solvent. This law is further supported by the fact that Raoult’s law empirically found for describing the behaviour of the solvent in dilute solutions can be deduced thermodynamically via the assumption of ideal behaviour of the solvent.
Answer the following questions:
(a) Give one example of miscible liquid pair which shows negative deviation from Raoult’s law. What is the reason for such deviation?
(b) (i) State Raoult’s law for a solution containing volatile components.
OR
(ii) Raoult’s law is a special case of Henry’s law. Comment.
(c) Write two characteristics of an ideal solution.