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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 64 g/mol (option b).

Step by step solution

01

Understand Raoult's Law

Raoult's Law states that the vapour pressure of a solvent is lowered by the addition of a non-volatile solute. The change in vapour pressure is proportional to the mole fraction of the solute in the solution. The formula is: \( P_{solution} = P_{solvent} \times \text{(mole fraction of solvent)} \).
02

Calculate the change in vapour pressure

The initial vapour pressure of pure acetone is 185 torr, and the vapour pressure when non-volatile solute is added is 183 torr. The change in vapour pressure is: \( \Delta P = 185 - 183 = 2 \) torr.
03

Determine the mole fraction of solute

Use the formula \( \Delta P = P_{solvent} \times X_{solute} \) to find the mole fraction of the solute. Rearranging gives \( X_{solute} = \frac{\Delta P}{P_{solvent}} = \frac{2}{185} \approx 0.0108 \).
04

Calculate moles of acetone

The molar mass of acetone is 58 g/mol. The moles of acetone in 100 g are given by \( \frac{100}{58} \approx 1.724 \) moles of acetone.
05

Use mole fraction to find moles of solute

Since \( X_{solute} + X_{solvent} = 1 \), we have \( X_{solvent} \approx 1 - 0.0108 = 0.9892 \). The mole fraction of solvent is also equal to \( \frac{\text{moles of solvent}}{\text{total moles}} \). Solving, we find the moles of solute \( n_{solute} \): \( n_{solute} = 0.0108 \times 1.734 \approx 0.0187 \).
06

Calculate the molar mass of the solute

We know \( m_{solute} = 1.2 \) g and \( n_{solute} = 0.0187 \) moles. Thus, the molar mass \( M = \frac{1.2}{0.0187} \approx 64 \) g/mol.

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Key Concepts

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

Vapour Pressure
Vapour pressure is a key concept in understanding how substances interact when they are combined in a solution. It is defined as the pressure exerted by the vapor in equilibrium with its liquid or solid form. This equilibrium is established when molecules escape from the liquid phase and enter the vapor phase at a constant rate, much like a fine mist above a calm lake.
In our context, we look at how the vapour pressure of a solvent changes when a solute (usually non-volatile) is added. The addition of a non-volatile solute decreases the vapour pressure of the solvent. This effect can be explained by the fact that solute molecules occupy space at the surface level where molecules escape into the gaseous state.
Raoult's Law serves as a useful tool here. It quantifies this decrease in vapour pressure in direct proportion to the mole fraction of the solute. For example, if a solvent has a vapour pressure of 185 torr, like pure acetone at a given temperature, and decreases to 183 torr upon adding a solute, it means the solute is actively affecting how readily acetone molecules can transition to the gas phase.
Mole Fraction
The mole fraction is a way of expressing the concentration of a component in a mixture. It's calculated by dividing the number of moles of one component by the total number of moles in the mixture. This value gives us an idea of the proportion of the entire mixture made up by that specific component.
When applying Raoult’s Law, understanding the mole fraction is crucial. It is symbolized as either \(X\), \(X_{solute}\) for solute, or \(X_{solvent}\) for solvent. For instance, in our exercise, the mole fraction is used to determine how the presence of the solute has altered the vapour pressure of acetone.
To find the mole fraction of the solute in our solution, we use the change in vapour pressure as part of Raoult's Law formula: \( \Delta P = P_{solvent} \times X_{solute} \). Solving for the mole fraction gives context to how much of a presence the solute has in the solution.
Non-Volatile Solute
A non-volatile solute is a substance that does not easily vaporize under existing conditions. Instead of readily escaping into the gas phase, it remains dissolved in the solvent. This property of non-volatility makes it a significant factor in altering the physical properties of solutions.
In our exercise, a non-volatile solute was added to acetone, affecting its vapour pressure. Since the solute does not contribute to vapour pressure, it only impacts the solvent’s behavior. By decreasing the number of molecules that can escape into the gas phase, the non-volatile component significantly lowers the vapour pressure.
The decrease in vapour pressure is helpful when calculating the molarity of a solute in a given solution. For instance, understanding that the solute's presence decreases the vapour pressure from 185 to 183 torr can help us deduce its mole fraction, leading us closer to its molar mass.
Molar Mass Calculation
Finding the molar mass of a solute involves integrating various pieces of information gathered from the experiment. Molar mass is a measure of the number of grams per mole of a substance, and it's instrumental in identifying and understanding substances.
In the exercise, we understood the change in vapour pressure, determined the mole fraction of the solute, and used these to identify the number of moles present. With the weight of the solute provided (1.2 grams) and the calculated number of moles (approximately 0.0187 moles), we can determine the molar mass using the formula:
  • \( Molar \ Mass \ (M) = \frac{mass\ of\ solute}{moles\ of\ solute} \)
Substituting the values into this formula gives us a molar mass of about 64 g/mol, allowing us to select the correct option from the choices given.

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Most popular questions from this chapter

The mass of glucose that should be dissolved in \(50 \mathrm{~g}\) of water in order to produce the same lowering of vapour pressure as is produced by dissolving \(1 \mathrm{~g}\) of urea in the same quantity of water is (a) \(1 \mathrm{~g}\) (b) \(3 \mathrm{~g}\) (c) \(6 \mathrm{~g}\) (d) \(18 \mathrm{~g}\)

In a depression in freezing point experiment, it is found that (1) the vapour pressure of the solution is less than that of pure solvent (2) the vapour pressure of the solution is more than that of pure solvent (3) only solute molecules solidify at the freezing point (4) only solvent molecules solidify at the freezing point (a) 1,2 (b) 2,3 (c) 1,4 (d) 1,3

If liquids A and B form an ideal solution, the (a) enthalpy of mixing is zero (b) entropy of mixing is zero (c) free energy of mixing is zero (d) free energy as well as the entropy of mixing are each zero

Benzene and toluene form nearly ideal solutions. At \(20^{\circ} \mathrm{C}\), the vapour pressure of benzene is 75 torr and that of toluene is 22 torr. The partial vapour pressure of benzene at \(20^{\circ} \mathrm{C}\) for a solution containing \(78 \mathrm{~g}\) of benzene and \(46 \mathrm{~g}\) of toluene in torr is (a) 25 (b) 50 (c) \(37.5\) (d) \(53.5\)

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