Asked by Lisa

Solve an equilibrium problem (using an ICE table) to calculate the pH of each solution: a solution that is 0.170 M in HC2H3O2 and 0.105 M in KC2H3O2

Answers

Answered by DrBob222
You don't need an ICE table to do this.
Use the Henderson-Hasselbalch equation.
Answered by Lisa
The book says to use ICE
Answered by DrBob222
OK. The book wants you to do it the hard way.
Here are the two equilibria.
......CH3COOH ==> H^+ + CH3COO^- for which
I.....0.170.......0......0
C......-x.........+x.....+x
E.....0.170-x.......x.......x

..........CH3COOK ==> K^+ + CH3COO^-
I.........0.105.......0.......0
C.........-0.105.....0.105...0.105
E.........0..........0.105.....0.105

Now write the Ka for CH3COOH.
Ka = (H^+)(CH3COO^-)/(CH3COOH)
So (H^+) = x
(CH3COO^- = x from CH3COOH and 0.105 from CH3COOK for a total of x+0.105
(CH3COOH) = 0.170-x, now plug all of that in
Ka = 1.8E-5 (but use the value in your text) = (x)(x+0.105)/(0.170-x)
We can avoid a quadratic equation by making a couple of simplifying assumptions.
x + 0.105 = 0.105 (since x will be small)
0.170-x = 0.170 (since x will be small) so now it looks this way.
1.8E-5=(x)(0.105)/0.170
Solve for x. I get 2.04E-5 for pH = 4.69. You shouldn't take my word for anything. Confirm all of this for yourself.
But look how much easier the HH equation makes things.
The HH equation is
pH = pKa + log [(base)/(acid)]
pKa = 4.74
base = 0.105
acid = 0.170
pH = 4.74+log(0.150/0.170 =
pH = 4.68
The small difference is in rounding errors.

Answered by emily
I agree that the Henderson-Hasslebalch equation is easier, but how do you find the pka without doing an ice table first?
Answered by Aiden
pKa = -log(Ka)
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