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The vapour pressure of acetone at \(20^{\circ} \mathrm{C}\) is 185 torr. When \(1.2 \mathrm{~g}\) of a non-volatile substance was dissolved in \(100 \mathrm{~g}\) of acetone at \(20^{\circ} \mathrm{C}\), its vapour pressure was 183 torr. The molar mass \(\left(\mathrm{g} \mathrm{mol}^{-1}\right)\) of the substance is (a) 32 (b) 64 (c) 128 (d) 488

Short Answer

Expert verified
The molar mass of the substance is 32 g/mol.

Step by step solution

01

Determine Change in Vapour Pressure

The change in vapour pressure when the substance is added can be calculated by subtracting the vapour pressure of the solution from the vapour pressure of pure acetone. So, the change is \(185\, \text{torr} - 183\, \text{torr} = 2\, \text{torr}\).
02

Calculate Relative Lowering of Vapour Pressure

The relative lowering of vapour pressure is given by \(\frac{\Delta P}{P_0} = \frac{2}{185}\), where \(\Delta P\) is the change in vapour pressure, and \(P_0\) is the original vapour pressure of acetone.
03

Apply the Formula for Molar Mass

Using the formula for the relative lowering of vapour pressure for solutions, we have \(\frac{\Delta P}{P_0} = \frac{n_2}{n_1 + n_2}\approx \frac{n_2}{n_1}\), since \(n_2\) (moles of solute) is much smaller than \(n_1\) (moles of solvent). Here, \(n_1 = \frac{100}{58} \approx 1.724\), as the molar mass of acetone is \(58 \text{ g/mol}\).
04

Calculate Moles of Solute

The relative lowering formula becomes \(\frac{2}{185} = \frac{1.2/M}{1.724}\), where \(M\) is the molar mass of the solute. Simplifying, \(\frac{1.2}{M} = \frac{2 \times 1.724}{185}\).
05

Solve for M

Rearrange and solve \(M = \frac{1.2 \times 185}{2 \times 1.724}\), which calculates to \(M \approx 32.06\). Thus, the closest molar mass option is \(32\, \text{g/mol}\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Relative Lowering of Vapour Pressure
The concept of relative lowering of vapour pressure is essential to understanding how solutions behave, especially when a solute is added to a solvent. When a non-volatile solute is dissolved in a solvent, the vapour pressure of the resulting solution decreases. This decrease is due to the fact that some of the solvent molecules at the surface are replaced by solute molecules, which do not evaporate. Thus, the overall number of solvent molecules that can escape into the vapour phase reduces. Relative lowering of vapour pressure can be expressed mathematically as:
  • \( \frac{\Delta P}{P_0} = \frac{P_0 - P_s}{P_0} \)
where \( \Delta P \) is the change in vapour pressure, \( P_0 \) is the vapour pressure of the pure solvent, and \( P_s \) is the vapour pressure of the solution. For our specific problem, the vapour pressure dropped from 185 torr to 183 torr upon adding the solute. This gives a relative lowering of vapour pressure as \( \frac{2}{185} \). Understanding this concept is crucial for calculating the molar mass of the solute in further steps.
Molar Mass Calculation
Calculating the molar mass of a solute in a solution involves using the concept of relative lowering of vapour pressure. From the previous concept, we learned how the vapour pressure changes. Now, using this change, the moles of solute can be correlated to the lost vapour pressure. The formula for this is:
  • \( \frac{\Delta P}{P_0} = \frac{n_2}{n_1} \)
Here, \( n_2 \) and \( n_1 \) are the moles of solute and solvent, respectively. Given that the molar mass of acetone, the solvent, is 58 g/mol, we can find the moles of solvent \( n_1 \) as:
  • \( n_1 = \frac{100}{58} \approx 1.724 \)
Substituting into the relative lowering equation, we solve for the molar mass \( M \) of the solute:
  • \( M = \frac{1.2 \times 185}{2 \times 1.724} \)
The outcome is approximately 32 g/mol, which matches close to option (a) 32 g/mol in the original choices.
Non-volatile Solute
A non-volatile solute is a substance that does not readily evaporate into the gas phase. This property is particularly useful in solutions where the goal is to reduce the vapour pressure without losing solute to evaporation. In our acetone example, the given solute is non-volatile, meaning it has little to no tendency to become a gas under the given conditions. When added to acetone, it stays in the liquid phase and replaces some of the acetone molecules that would otherwise contribute to vapour pressure. This results in a lowered vapour pressure for the solution compared to the pure solvent. Knowing about non-volatile solutes is essential for understanding colligative properties such as vapour pressure lowering, boiling point elevation, and freezing point depression. Since these properties depend on the number of solute particles rather than their identity, they are crucial in calculating attributes like molar mass. By grasping how non-volatile solutes function, students can better predict how solutions behave in real-world applications, such as antifreeze in car radiators or in processes like distillation.

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Most popular questions from this chapter

When mercuric iodide is added to the aqueous solution of potassium iodide, the (a) freezing point is raised (b) freezing point does not change (c) freezing point is lowered (d) boiling point does not change

The colligative properties of electrolytes require a slightly different approach than the one used for the colligative properties of non- electrolytes. The electrolytes dissociate into ions in solution. It is the number of solute particles that determine the colligative properties of a solution. The electrolyte solutions, therefore show abnormal colligative properties. To account for this effect we define a quantity; called the van't Hoff factor which is given by [solution] \(i=\) \(\frac{\text { Actual number of particles in solution after dissociation }}{\text { Number of formula units initally dissolved in solution }}\) \(\mathrm{i}=1\) (for non - electrolytes); \(\mathrm{i}>1\) (for electrolytes, undergoing dissociation) \(\mathrm{i}<1\) (for solute, undergoing association) For a solution of a non electrolyte in water, the van't Hoff factor is (a) Always equal to 2 (b) Always equal to 0 (c) \(>1\) but \(<2\) (d) \(\leq 1\)

Which of the following statement is true about ideal solutions? (a) the volume of mixing is zero (b) the enthalpy of mixing is zero (c) both \(\mathrm{A}\) and \(\mathrm{B}\) (d) none of these

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