Step 3: Substitute into the equilibrium expression known (and unknown) information. Let x
equal the amount of H+that ionizes from HA. Because the molar ratio of [H+]:[A–] is 1:1, [A–]
also equals x, and we can approximate 0.50 −x as 0.50 (5% rule).
174 10.^5050 .x
2
# - =
Step 4: Solve for x.
x^2 = (1.74 × 10 –5)(0.50)
= 8.7 × 10 –6
x = 2.9 × 10 –3M = [H+]
(b) Restatement: pH and pOH in 0.50 M HA.
pH = −log[H+] = −log (2.9 × 10 –3) = 2.47
pH + pOH = 14
pOH = 14.0 −2.47 = 11.53
Note: Significant figures for logarithms is equal to the number of significant figures in the
mantissa.
(c) Restatement: % HA that does ionize.
%%%WholePart
HA
H
## 100 = 100
+
6
7
@
A
.
. %.%
050
==29 10# -^3 # 100 0 58
However, 0.58% represents the percentage of the HA molecules that doionize. Therefore,
100.00 −0.58 = 99.42% of the HA molecules do notionize.
(d) Given: Buffer pH = 6.50
Restatement: [HA]/[A–]?
Step 1: Recognize the need to use the Henderson-Hasselbalch equation.
log
acid
base
pH p= Ka+ (^106)
6
@
@
Step 2: Substitute into the equation the known (and unknown) information.
pKa= −log Ka= 4.76
.. log
HA
A
65 476=+
6
7
@
A
log ...
HA
A
=-=6 50 4 76 1 74
6
7
@
A
.
HA
A
=55 10#^1
6
7
@
A
Because the question is asking for [HA] / [A–], you need to take the reciprocal: 0.018 155
Equilibrium