What is the mol fraction of ethylene glycol in the solution phase for an aqueous solution with a vapor pressure of #"760 torr"# if the pure vapor pressure was #"1077 torr"#?
As per Raoult's law:
where
There was a drop in vapor pressure because the solution's total vapor pressure—which is less than the pure vapor pressure of water—was disclosed.
To monitor that alteration:
After that, applying Raoult's law:
The shift in pressure was:
Thus, if ethylene glycol were present in the solution rather than the vapor phase, its mole fraction would be:
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The mole fraction of ethylene glycol in the solution phase can be calculated using Raoult's law, which states that the vapor pressure of a solution is proportional to the mole fraction of each component in the solution. The formula to calculate the mole fraction ((X)) of ethylene glycol in the solution phase is:
[X = \frac{{P_{\text{{ethylene glycol}}}}}{{P_{\text{{ethylene glycol}}} + P_{\text{{water}}}}]
Given that the vapor pressure of the solution ((P_{\text{{solution}}})) is equal to the vapor pressure of water ((P_{\text{{water}}})) due to Raoult's law, we can set:
[P_{\text{{solution}}} = P_{\text{{water}}} = 760 , \text{{torr}}]
The vapor pressure of pure ethylene glycol ((P_{\text{{ethylene glycol}}})) is given as (1077 , \text{{torr}}). Plugging in these values into the formula for the mole fraction, we can calculate (X).
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To calculate the mole fraction of ethylene glycol ((X_{EG})) in the solution phase, you can use Raoult's law:
[P_{solution} = X_{EG} \times P_{EG} + (1 - X_{EG}) \times P_{water}]
Given: [P_{solution} = 760 \text{ torr}] [P_{EG} = 1077 \text{ torr}] [P_{water} = 760 \text{ torr}]
Rearranging the equation to solve for (X_{EG}):
[X_{EG} = \frac{P_{solution} - P_{water}}{P_{EG} - P_{water}}]
Substituting the given values:
[X_{EG} = \frac{760 - 760}{1077 - 760}]
[X_{EG} = \frac{0}{317}]
[X_{EG} = 0]
So, the mole fraction of ethylene glycol in the solution phase ((X_{EG})) is 0.
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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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