Question #a2062

1 Answer
Sep 22, 2017

4%

Explanation:

The dissociation equilibrium for your weak acid "HA" can be written as follows

"HA"_ ((aq)) + "H"_ 2"O"_ ((l)) rightleftharpoons "H"_ 3"O"_ ((aq))^(+) + "A"_ ((aq))^(-)

By definition, the acid dissociation constant, K_a, is equal to--keep in mind that the concentrations of pure liquids are not added to the expression of the acid dissociation constant!

K_a = (["H"_3"O"^(+)] * ["A"^(-)])/(["HA"])

Now, you know that for every 1 mole of "HA" that dissociates, you get 1 mole of hydronium cations and 1 mole of "A"^(-), the conjugate base of the acid.

This means that, at equilibrium, you have

["H"_3"O"^(+)] = ["HA"] = x

The equilibrium concentration of the weak acid will be equal to

["HA"] = ["HA"]_ 0 - x

This basically tells you that in order to have x "M" of hydronium cations and of "A"^(-) in the solution, you need to consume x "M" of the weak acid.

Plug this into the expression of the acid dissociation constant to get--keep in mind that you have ["HA"]_0 = "0.50 M"

K_a = (x * x)/(0.50 -x)

K_a = (x^2)/(0.50 -x)

Now, because the value of the acid dissociation constant is very small compared to the initial concentration of the acid, you can use the following approximation

0.50 - x ~~ 0.50

This means that you have

8 * 10^(-4) = x^2/0.50

Rearrange to solve for x

x = sqrt(0.50 * 8 * 10^(-4)) = 0.02

This means that, at equilibrium, this solution contains

["H"_3"O"^(+)] = "0.02 M"

At this point, you need to check the approximation by using

(["H"_3"O"^(+)])/(["HA"]_0) * 100% < color(red)(5%)

You will have

(0.02 color(red)(cancel(color(black)("M"))))/(0.50color(red)(cancel(color(black)("M")))) * 100% = 4% < color(red)(5%)

This means that the approximation holds.

Moreover, this represents the percent dissociation of the acid, so you can say that

color(darkgreen)(ul(color(black)("% dissociation" = 4%)))

This means that for every 100 molecules of "HA" present in the solution only 4 will dissociate to produce hydronium cations and "A"^(-).