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taurus [48]
3 years ago
6

4. An ideal solution contains 40 mole percent of A and 60 mole percent of B at 80 oC. The vapor pressure of pure A and B at this

temperature are 480 torr and 890 torr, respectively. Calculate the vapor pressure of the solution.
Chemistry
1 answer:
Vikentia [17]3 years ago
6 0

Answer :  The vapor pressure of the solution is, 726 torr.

Explanation : Given,

Mole percent of A = 40 %

Mole fraction of A = 0.4

Mole percent of B = 60 %

Mole fraction of A = 0.6

Now we have to calculate the partial pressure of A and B.

According to the Raoult's law,

p_i=X_i\times p^o_i

where,

p_i = vapor pressure of gas

p_^o_i = vapor pressure of pure gas  

X_i = mole fraction of gas

p_{A}=X_{A}\times p^o_A

p_{A}=0.4\times 480torr=192torr

and,

p_{A}=X_{A}\times p^o_A

p_{A}=0.6\times 890torr=534torr

Now we have to calculate the vapor pressure of the solution.

P_T=p_{A}+P_{B}

P_T=192torr+534torr

P_T=726torr

Thus, the vapor pressure of the solution is, 726 torr.

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Who conducted experiments to determine the quantity of charge carried by an electron?
MAXImum [283]

Answer:

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What is the mass of and object with a volume of 100 cm3 and a density of 10 g/cm3?
nadezda [96]

Answer:

1000 g

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4 0
3 years ago
You determine that it takes 26.0 mL of base to neutralize a sample of your unknown acid solution. The pH of the solution when ex
mojhsa [17]

Answer:

a. 1.78x10⁻³ = Ka

2.75 = pKa

b. It is irrelevant.

Explanation:

a. The neutralization of a weak acid, HA, with a base can help to find Ka of the acid.

Equilibrium is:

HA ⇄ H⁺ + A⁻

And Ka is defined as:

Ka = [H⁺] [A⁻] / [HA]

The HA reacts with the base, XOH, thus:

HA + XOH → H₂O + A⁻ + X⁺

As you require 26.0mL of the base to consume all HA, if you add 13mL, the moles of HA will be the half of the initial moles and, the other half, will be A⁻

That means:

[HA] = [A⁻]

It is possible to obtain pKa from H-H equation (Equation used to find pH of a buffer), thus:

pH = pKa + log₁₀ [A⁻] / [HA]

Replacing:

2.75 = pKa + log₁₀ [A⁻] / [HA]

As [HA] = [A⁻]

2.75 = pKa + log₁₀ 1

<h3>2.75 = pKa</h3>

Knowing pKa = -log Ka

2.75 = -log Ka

10^-2.75 = Ka

<h3>1.78x10⁻³ = Ka</h3>

b. As you can see, the initial concentration of the acid was not necessary. The only thing you must know is that in the half of the titration, [HA] = [A⁻]. Thus, the initial concentration of the acid doesn't affect the initial calculation.

7 0
3 years ago
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