If a solvent contains a few impurities, how does its boiling point compare to the pure solvent?
The boiling point of the compound will be slightly elevated.
Usually, the boiling point of a liquid has a rising temperature gradient. Impurities elevate the boiling point, and the elevation is proportional to their concentration.
As the distillation proceeds, the concentration of the impurity (left in the still pot) becomes greater and boiling point becomes higher. A second distillation of the first collected fraction is usually performed, and this gives a much more stable distillation profile in that the distillate is more pure, and a much better measurement of the boiling point may be achieved.
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In considering boiling point, we are likely talking about a liquid. When dissolving something unlike the liquid in the liquid, you add impurities into the liquid.
Consider the following expression, derived from the Gibbs-Duhem relation (Physical Chemistry: A Molecular Approach, Ch. 24-2, pg. 968):
#\mathbf(mu_j = mu_j^"*" + RTlnchi_j)# where:
#mu_j# is the chemical potential, or the partial molar free energy, of component#j# in solution. It is similar in principle to potential energy in that substances generally want to minimize chemical potential.#R# is the universal gas constant#T# is temperature in#"K"# #chi_j# is the mole fraction of component#j# in solution. It could be written as#(n_j)/(n_i + n_j)# for a solution containing components#i# and#j# , where#n_j# is the number of#"mol"# s of component#j# .#"*"# is the IUPAC notation for a pure substance, i.e. one that is not mixed with anything other than itself.
WHAT IF WE DISSOLVE SOMETHING IN THE SOLUTION?
If we suppose a liquid organic compound
#mu_j = mu_j^"*" + RT ln (chi_j color(blue)( + x))# where
#x# is the fraction of the solution that is no longer made up of#j# , meaning that#chi_j + x = 1# .Since
#chi_j# of a pure solution is#1# (the mole fraction of#j# in solution#j# when it is composed of only#j# is#100%# ), when#chi_j + x = 1# ,#0 < chi_j < 1# .When
#0 < chi_j < 1# , we have#lnchi_j < 0# , and therefore,#RTlnchi_j < 0# . So,#mu_j < mu_j^"*"# , so the chemical potential of the solution has decreased.Now consider the following diagram, which examines the chemical potential vs. the temperature at a constant pressure:
When crossing over to a different phase (e.g. solid
#-># liquid#-># gas), the slope abruptly changes, demonstrating a difference in entropy magnitudes between a solid, liquid, and a gas, and the graph reflects that because#((delmu)/(delT))_P = -S# .Right now, the graph shows
#mu_j^"*"# vs.#T# . We are looking at the liquid, so when#mu_j# for the liquid decreases,#mu_j < mu_j^"*"# , meaning that the straight line for the liquid moves downwards.Since the intersections indicate the boiling and freezing points, the boiling point has shifted to the right, and therefore, the boiling point increases.
This is why there is some boiling point elevation when you dissolve a solute into a solvent.
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The boiling point of a solvent containing impurities will be slightly higher than that of the pure solvent. This phenomenon is known as boiling point elevation. The presence of impurities disrupts the regularity of the solvent molecules, making it more difficult for them to escape into the gas phase. As a result, a higher temperature is required to reach the boiling point, leading to an elevation in the boiling point compared to the pure solvent.
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If a solvent contains impurities, its boiling point will be higher than that of the pure solvent. This phenomenon is known as boiling point elevation. The presence of impurities disrupts the regular crystal lattice structure of the solvent, making it more difficult for the solvent molecules to escape into the vapor phase. As a result, the solvent requires more energy (heat) to reach its boiling point, leading to an increase in the boiling point compared to the pure solvent.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
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