Acid Base Equilibria Notes
Acid Base Equilibria Notes
This Table of
Contents is
1 Acids and Base Definitions clickable!
2 Strong and Weak Acids
4 Strong and Weak Bases
5 Acid-Base Neutralization Reactions
6 Conjugate Acids and Bases
9 Amphoteric Species
10 Autoionization
11 What is pH?
12 Significant Figure Rules for pH and pOH
13 Finding the pH of a Strong Acid
15 Finding the [H 3 O + ] of a Strong Acid
16 Finding the pOH of a Strong Base
17 Finding the [OH - ] of a Strong Base
18 Finding pH from [OH - ]
19 Finding the pH of a Strong Base
21 Finding [OH - ] from pH
22 Finding pH and pOH
23 Finding [OH - ] from [H 3 O + ]
24 Finding [H 3 O + ] from [OH - ]
25 Summary of All Formulas
26 What is K a ?
27 What is K b ?
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28 How to Build an ICE Table
31 How to Use the 5% Rule
32 When to Use the Quadratic Formula
34 Finding the pH of a Weak Acid
48 Finding the pH of a Weak Base
58 Main Steps for Finding pH of Acids and Bases
59 Finding K a and K b
64 Percent Ionization
74 Relationship between pKa and pKb
77 Finding Mass from pH
78 pH and Ideal Gas Law Question
81 Finding Volume using Density
83 Properties of Anions and Salts
84 Properties of Cations and Salts
85 Classifying Salts as Acidic, Basic or Neutral
91 Determining Acid Strength
94 Finding pH of a Solution with an Anion
98 Mixtures of Acids
example: HBr H + + Br -
example: NaOH Na + + OH -
example: HCl + NH 3 NH +4 + Cl -
Base Gains H +
example: HBr H + + Br -
example: HC 2 H 3 O 2 H + + C 2 H 3 O-2
Note:
All the below words refer to the acid splitting apart into its separate
ions. Ions are elements with a charge.
• Dissociate • Dissociation
• Ionize • Ionization
HI Hydroiodic acid HI H+ + I-
TIP: Strong bases are typically groups 1 & 2 metals combined with OH -
NH 3 Ammonia NH 3 + H 2 O NH4+ + OH -
C 6 H 5 NH 2 Aniline C 6 H 5 NH 2 + H 2 O C 6 H 5 NH+3 + OH -
CH 3 NH 2 Methylamine CH 3 NH 2 + H 2 O CH 3 NH+3 + OH -
Predicting Products:
HCl + NaOH • Combine the inner elements, starting with the
metal (+ charge) then the nonmetal (- charge).
These form an ionic compound which is the Salt.
Na + Cl - • Combine the outer elements, these form water.
H + OH -
Balanced Chemical Equation: HCl + NaOH NaCl + H 2 O
Acid Base Salt Water
Balance Charges
H 2 SO4 + LiOH
Li + SO2 -
4
Li + SO42 -
Li + SO42 -
Li 2 SO4
H + OH -
Balance Charges
H 3 PO4 + KOH
K + PO3 -
4
K + PO43 -
K + PO43 - K 3 PO4
H + OH -
HA + B HB + + A -
Acid + Base Conjugate Acid + Conjugate Base
HCl + NH 3
Base accepts H + and becomes new conjugate acid.
Step
2
HCl + NH 3 NH+4
Acid loses H + and becomes new conjugate base.
Step
3
HCl + NH 3 NH+4 + Cl -
Acid loses H +
HBr + H 2 O
Base accepts H + and becomes new conjugate acid.
Step
2
HBr + H 2 O H3O+
Acid loses H + and becomes new conjugate base.
Step
3
HBr + H 2 O H 3 O + + Br -
Acid Base Conjugate Acid Conjugate Base
Step
1
Acid donates H + to Base.
H 2 SO4 + H 2 O
Step
2 Base accepts H + and becomes new conjugate acid.
H 2 SO4 + H 2 O H3O+
Step
3
Acid loses H + and becomes new conjugate base.
H 2 SO4 + H 2 O H 3 O + + HSO4-
Acid Base Conjugate Acid Conjugate Base
B HB +
Base Conjugate Acid Charges:
Gaining an H + means
Base gains H + you add +1 to the charge.
CN - HCN CN - HCN
-1 Charge + 1 H + = 0 (No Charge)
Base Conjugate Acid
CO 32 - HCO 3-
-2 Charge + 1 H + = -1 Charge
Base gains H +
2-
CO 3 HCO 3-
Base Conjugate Acid
HA A-
Acid Conjugate Base Charges:
Losing an H + means you
Acid loses H + subtract 1 from the charge.
H 2 O + HCO 3- H 2 CO 3 + OH -
Acid Base Conjugate Acid Conjugate Base
H 2 O acts as an acid.
H 2 O + NH 3 NH4+ + OH -
Acid Base Conjugate Acid Conjugate Base
H2O + H2O H 3 O + + OH -
Acid Base Conjugate Acid Conjugate Base
• The equilibrium constant for water when it’s reacting with itself.
K w = [H 3 O + ] x [OH - ] OR K w = [H + ] x [OH - ]
• Numerical value.
Note:
K w = 1.0 x 10 - 14 Has no units
[H 3 O + ] and [H + ]
• We can set everything equal to each other. both refer to the
concentration of acid
K w = 1.0 x 10 - 14 = [H 3 O + ] x [OH - ]
[H 3 O + ] = 1.0 x 10 - 7
In a neutral solution at 25°C
[OH - ] = 1.0 x 10 - 7
pH Ion Concentration
[H 3 O + ] > [OH - ]
pH < 7 More acid than base
pH = 0 - 6 [H 3 O + ] > 1.0 x 10 - 7
[OH - ] < 1.0 x 10 - 7
pH Ion Concentration
[H 3 O + ] = [OH - ]
Equal amounts of acid and base
pH = 7 [H 3 O + ] = 1.0 x 10 - 7
[OH - ] = 1.0 x 10 - 7
pH Ion Concentration
[H 3 O + ] < [OH - ]
pH > 7 More base than acid
pH = 8 - 14 [H 3 O + ] < 1.0 x 10 - 7
[OH - ] > 1.0 x 10 - 7
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
Concentration to pH or pOH:
Given: [H 3 O + ] = 4.1 x 10 -4 M
pH = 3.39
The amount of decimal places the pH or pOH has equals the number of
sig figs the concentration will have.
pH or pOH to Concentration:
Given: pH = 3.39
[H 3 O + ] = 4.1 x 10 -4 M
Formula
pH = -log [H 3 O + ] or pH = -log [H + ]
[H 3 O + ] to pH:
Step
1 Since we are given the concentration of HCl which is a strong
acid, then that really means we are given [H 3 O + ].
pH = -log [H O + ] 3
pH = -log [0.11]
pH = 0.9586073148
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 0.11
2 sig figs = 2 decimal places
pH = 0.9586073148
Round up to 2 decimal places
pH = 0.96
[H 3 O + ] = 2(0.25)
[H 3 O + ] = 0.50 M
pH = -log [0.50]
pH = 0.3010299957
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 2 SO4 ] = 0.25 M
pH = 0.30
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14
Finding the [H 3 O + ] of a Strong Acid
Formula
[H 3 O + ] = 10 - pH or [H + ] = 10 - pH
pH to [H 3 O + ]
Given: pH = 5.6
[H 3 O + ] = 10 - pH
[H O + ] = 10 - 5.6
3
[H O + ] = 2.511886432 x 10 - 6
3
The amount of decimal places the pH or pOH has equals the number of
sig figs the concentration will have.
pH = 5.6
1 decimal place = 1 sig fig
[H 3 O + ] = 2.511886432 x 10 - 6
Round up to 1 sig fig
[H 3 O + ] = 3 x 10 - 6
Formula
pOH = -log [OH - ]
[OH - ] to pOH
Calculate the pOH of a 0.025 M solution of NaOH.
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[OH - ] = 0.025
2 sig figs = 2 decimal places
pOH = 1.602059991
Round to 2 decimal places
pOH = 1.60
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16
Finding the [OH - ] of a Strong Base
Formula
[OH - ] = 10 - pOH
pOH to [OH - ]
The amount of decimal places the pH or pOH has equals the number of
sig figs the concentration will have.
pOH = 2.1
1 decimal place = 1 sig fig
[OH - ] = 0.0079432823
Round up to 1 sig fig
[OH - ] = 0.008
Make sure units are in molarity (M) since this is the concentration
Step
3
of base.
[OH - ] = 0.008 M
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[OH - ] = 0.0020
2 sig figs = 2 decimal places
pOH = 2.698970004
Round up to 2 decimal places
pOH = 2.70
Step
4 Find pH by plugging in pOH into the formula.
pH + pOH = 14
pH + 2.70 = 14
- 2.70 - 2.70 subtract 2.70 from both sides
pH = 11.3
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18
Finding the pH of a Strong Base
Trick Question
Calculate the pH of a 7.5 x 10 - 6 M Mg(OH) 2 solution.
Note
We cannot just plug in the base concentration into any formula yet.
[OH - ] ≠ [Mg(OH) ] 2
This is because there's twice the amount of base concentration.
The 2 subscript on Mg(OH) 2 tells us 2 hydroxides dissociate.
2 [OH - ] = [Mg(OH) ] 2
[OH - ] = 2 (7.5 x 10 - 6 )
[OH - ] = 1.5 x 10 - 5 M
[H 3 O + ](1.5 x 10 - 5 ) = 1.0 x 10 - 14
[H 3 O + ](1.5 x 10 - 5 ) = 1.0 x 10 - 14
1.5 x 10 - 5 1.5 x 10 - 5
[H O + ] = 6.66666667 x 10 - 10 M
3
Round to 2 sig figs
[H 3 O + ] = 6.7 x 10 - 10 M
pH = -log [6.7 x 10 - 10 ]
pH = 9.175874166
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[Mg(OH) 2 ] = 7.5 x 10 - 6 M
pH = 9.175874166
Round up to 2 decimal places
pH = 9.18
Given: pH = 8.7
pH + pOH = 14
8.7 + pOH = 14
- 8.7 - 8.7 subtract 8.7 from both sides
pOH = 5.3
Find [OH - ] by plugging in pOH into the formula.
Step
2
[OH - ] = 10 - pOH
[OH - ] = 10 - 5.3
[OH - ] = 5.011872336 x 10 - 6 M
Step
3
Round to the correct amount of sig figs.
pOH = 5.3
1 decimal place = 1 sig fig
[OH - ] = 5.011872336 x 10 - 6 M
Round to 1 sig fig
[OH - ] = 5 x 10 - 6 M
pOH to pH
pH to pOH
Given: pH = 9.7
pH + pOH = 14
9.7 + pOH = 14
- 9.7 - 9.7 subtract 9.7 from both sides
pOH = 4.3
[H 3 O + ] to [OH - ]
Given: [H 3 O + ] = 2.7 x 10 - 4 M
[H 3 O + ] x [OH - ] = 1.0 x 10 - 14
[OH - ] to [H 3 O + ]
[H 3 O + ] x [OH - ] = 1.0 x 10 - 14
[H O + ] x 3.4 x 10 - 8 = 1.0 x 10 - 14
3
[H 3 O + ] x 3.4 x 10 - 8 = 1.0 x 10 - 14
divide 3.4 x 10 - 8 from both sides
3.4 x 10 - 8 3.4 x 10 - 8
[H 3 O + ] = 2.941176471 x 10 - 7 M
Round to 2 sig figs since the given only has 2 sig figs
[H 3 O + ] = 2.9 x 10 - 7 M
pH = -log [H 3 O + ] [H 3 O + ] = 10 - pH
pH to pOH [H 3 O + ] to [OH - ]
or or
pOH to pH -
[OH ] to [H 3 O + ]
[OH - ] to pH pH to [OH - ]
[H 3 O + ][A - ] [H + ][A - ]
K = or K a =
a [HA] [HA]
The value of K a tells us the strength of the acid:
K a the stronger the acid and pH.
K a the weaker the acid and pH.
d, because K a the weaker the acid and since 10 - 10 is the lowest, it is the weakest.
[BH + ][OH - ]
K b =
[B]
c, because K b the weaker the base and since 10 - 13 is the lowest, it is the weakest.
I = Initial concentration
C = Change in concentration
HA + H2O H3O+ + A-
C -x +x +x
Step
1 Start with adding initial concentration values to the first line.
H 2 O is excluded in an ICE Table.
HA + H2O H3O+ + A-
HA + H2O H3O+ + A-
I Initial Acid Concentration 0 0
C -x +x +x
HA + H2O H3O+ + A-
C -x +x +x
HCOOH + H 2 O H 3 O + + COOH -
I 0.100 0 0
HCOOH + H 2 O H 3 O + + COOH -
I 0.100 0 0
C -x +x +x
HCOOH + H 2 O H 3 O + + COOH -
I 0.100 0 0
C -x +x +x
E 0.100 - x x x
This rule states that if x is small then it will not drastically change the
initial concentration of the acid or base, the change is negligible.
Build an ICE Table and set Assume x is small for now, only to
Step Step
1 2
up the K a expression. check if the 5% rule is valid or not.
H 2 X + H 2 O H 3 O + + HX -
Apply the “x is small assumption” by
I 0.10 0 0 removing the x that is being subtracted.
1.20 x 10 -3 = x2
C -x +x +x 0.10 - x
1.20 x 10 -3 = x2
E 0.10 - x x x
0.10
Multiply both sides by 0.10.
Write the K a expression for the
above chemical equation. x2
0.10 x 1.20 x 10 -3 = x 0.10
0.10
[Products] coefficient 1.20 x 10 -4 = x 2
Ka =
[Reactants] coefficient Take the square root of both sides.
[H 3 O + ][HX - ]
Ka = 1.20 x 10 -4 = x2
[H 2 X]
x = 0.011
x2
Ka =
0.10 - x Step
Check if the 5% rule is valid.
3
Plug in the given K a value into the x
K a expression. 5% Rule = x 100
[initial acid]
Given: K a = 1.20 x 10 -3 0.011
5% Rule = x 100 = 11%
x2 0.10
1.20 x 10 -3 =
0.10 - x Since 11% is greater than 5%, the rule is
invalid, we cannot cancel out x and we must
use the quadratic formula.
Clue Since our K a > 10 -4 the 5% rule
will be invalid.
Add values
Move all values on the left side to -1.20 x 10 - 3 ± 1.44 x 10 - 6 + 4.8 x 10 - 4
the right side so that the left side x=
equals zero. 2
Take the square root
Add 1.20 x 10 -3 x to both sides
-1.20 x 10 - 3 ± 4.8144 x 10 - 4
1.20 x 10 -4 - 1.20 x 10 -3 x = x 2 x=
2
+ 1.20 x 10 -3 x + 1.20 x 10 -3 x
-1.20 x 10 - 3 ± 0.021941741
1.20 x 10 -4 = x 2 + 1.20 x 10 -3 x x=
2
Separate into two fractions
-1.20 x 10-3 + 0.021941741 -1.20 x 10-3 - 0.021941741
Subtract 1.20 x 10 -4 to both sides. 2 2
[H 3 O + ] ≠ [weak acid]
This is why we must use an ICE table and the K a to find the acid
concentration, [H 3 O + ], at equilibrium.
x•x
x 10 - 8 =
1.5
0.20 - x
x•x
x 10 - 8 =
1.5
0.20 - x
- 8 x2
1.5 x 10 =
0.20 - x
Multiply the
denominator to both sides.
-8 x2
(0.20) x 1.5 x 10 = x (0.20)
0.20
3.0 x 10 - 9 = x 2
3.0 x 10 - 9 = x2
5.477225575 x 10 - 5 = x
[H 3 O + ] = 5.5 x 10 - 5 M pH = -log [H 3 O + ]
pH = -log [5.5 x 10 - 5 ]
pH = 4.259637311
Step
7
Round to the correct amount of sig figs.
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 5.5 x 10 - 5 M
2 sig figs = 2 decimal places
pH = 4.259637311
Round up to 2 decimal places
pH = 4.26
H + (aq) + C 2 H 3 O 2- (aq)
HC 2 H 3 O 2 (aq) [H + ][C 2 H 3 O 2- ]
K a =
I 0.52 0 0 [HC 2 H 3 O 2 ]
C -x
+x +x
K a = 1.8 x 10 - 5
E 0.52 - x x x
x •x
1.8 x 10 - 5 =
0.52 - x
Multiply the numerator.
x •x
1.8 x 10 - 5 =
0.52 - x
x 2
1.8 x 10 - 5 =
0.52 - x
- 5 x2
1.8 x 10 =
0.52
- 5 x2
(0.52) x 1.8 x 10 = x (0.52)
0.52
- 6
9.36 x 10 = x 2
-6 = x2
9.36 x 10
0.0030594117 = x
[H 3 O + ] = 0.0031 M pH = -log [H 3 O + ]
pH = -log [0.0031]
pH = 2.508638306
Step
7 Round to the correct amount of sig figs.
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 0.0031 M
2 sig figs = 2 decimal places
pH = 2.508638306
Round up to 2 decimal places
pH = 2.51
Calculate the pH of a 0.020 M HClO 2 solution,
-2
K a for HClO 2 is 1.0 x 10 .
Step
2
Write the Dissociation Equation.
HClO 2 (aq) H + (aq) + ClO 2- (aq)
Step
4 Write the K a expression.
equilibruium expression
[H + ][ClO 2- ]
Ka =
[HClO 2 ]
- x•x
1.0 x 10 2 =
0.020 - x
2 x2
-
1.0 x 10 =
0.020 - x
0.020 - x
a
Do not cancel out x, instead use the quadratic formula
2.0 x 10 - 4 - 1.0 x 10 - 2 x = x 2
descending order: ax 2 + bx - c
2.0 x 10 - 4 - 1.0 x 10 - 2 x = x 2
+ 1.0 x 10 - 2 x + 1.0 x 10 - 2 x
2.0 x 10 - 4 = x 2 + 1.0 x 10 - 2 x
2.0 x 10 - 4 = x 2 + 1.0 x 10 - 2 x
-2.0 x 10 - 4 -2.0 x 10 - 4
0 = x 2 + 1.0 x 10 - 2 x - 2.0 x 10 - 4
0 = 1 x 2 + 1.0 x 10 - 2 x -2.0 x 10 - 4
If no coefficient is
shown, assume it is 1
a = 1 b = 1.0 x 10 - 2 c = -2.0 x 10 - 4
[H 3 O + ] = 0.010 M pH = -log [H 3 O + ]
pH = -log [0.010]
pH = 2
Round to the correct amount of sig figs.
Step
7
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 0.010 M
2 sig figs = 2 decimal places
pH = 2
Add 2 decimal places
pH = 2.00
Due to these differences you will need to add a step and find the [H 3 0 + ]
using [OH - ].
C -x +x +x
E 0.100 - x x x
x•x
1.76 x 10 - 5 =
0.100 - x
- 5 x2
1.76 x 10 =
0.100 - x
Multiply the
denominator to both sides.
- 5 x2
(0.100) x 1.76 x 10 = x (0.100)
0.100
1.76 x 10 - 6 = x 2
1.76 x 10 - 6 = x2
0.0013266499 = x
[H 3 O + ] = 7.51879699 x 10 - 12 M
found looking at the given values
Given: 0.100 M B
Round up to 3 sig figs K b = 1.76 x 10 - 5
[H 3 O + ] = 7.52 x 10 - 12 M
Find pH by using pH = -log [H 3 O + ].
Step
7
pH = -log [7.52 x 10 - 12 ]
pH = 11.12378216
Round to the correct amount of sig figs.
Step
8
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 7.52 x 10 - 12 M
3 sig figs = 3 decimal places
pH = 11.12378216
Round up to 3 decimal places
pH = 11.124
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52
Finding the pH of a Weak Base
Determine the pH of a 0.0043 M CH 3 NH 2 solution with
-4
a K b of 4.4 x 10 .
Step
4 Write the K b expression.
equilibruium expression
- x•x
4.4 x 10 4 =
0.0043 - x
4 x2
-
4.4 x 10 =
0.0043 - x
x2
4.4 x 10 - 4 =
0.0043
1.892 x 10 - 6 = x 2
1.892 x 10 - 6 = x2
0.0013754999 = x
0.0013754999 = x
Plug in [OH - ] = 0.0014.
[H 3 O + ][OH - ] = 1.0 x 10 - 14
[H 3 O + ][0.0014] = 1.0 x 10 - 14
[H 3 O + ](0.0014) = 1.0 x 10 - 14
0.0014 0.0014
[H O + ] = 7.14285714 x 10 - 12 M
3
[H 3 O + ] = 7.14285714 x 10 - 12 M
Round to 2 sig figs Correct amount of sig figs is
found looking at the given values
[H 3 O + ] = 7.1 x 10 - 12 M
Given: 0.0043 M CH 3 NH 2
K b = 4.4 x 10 - 4
pH = -log [7.1 x 10 - 12 ]
pH = 11.14874165
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 7.1 x 10 - 12 M
2 sig figs = 2 decimal places
pH = 11.14874165
Round up to 2 decimal places
pH = 11.15
K a x K b = 1.0 x 10 - 14 K a x K b = 1.0 x 10 - 14
Step
1 Identify the given and what you're finding.
Given: 0.10 M HC 3 H 5 O 3 Find: K a
pH = 2.44
Find [H O + ] using [H O + ] = 10 - pH .
Step
2
3 3
[H 3 O + ] = 10 - 2.44 Correct amount of sig figs is
[H 3 O + ] = 0.0036 M
[H 3 O + ][C 3 H 5 O 3- ]
K =
a [HC 3 H 5 O 3 ]
Step
Solve for the K a value by plugging in the equilibrium concentrations into
7
the K a expression.
(0.0036)(0.0036)
K a =
0.10
1.296 x 10 - 5
K a =
0.10
K a = 1.296 x 10 - 4
Round up to 2 sig figs
K a = 1.3 x 10 - 4
Sodium benzoate, C 6 H 5 CO 2 Na, is the salt of the weak acid benzoic acid
(C 6 H 5 CO 2 H). A 0.10 M solution of sodium benzoate has a pH of 8.60.
Calculate the K b value for the benzoate ion (C 6 H 5 CO -2).
Step
1 Identify the given and what you're finding.
Given: 0.10 M C 6 H 5 CO 2 Na Find: K b
pH = 8.60
Find pOH using pH + pOH = 14.
Step
2
given pH value
8.60 + pOH = 14
Subtract 8.60 to both sides
8.60 + pOH = 14
-8.60 -8.60
pOH = 5.40
[OH - ] = 10 - 5.40
[OH - ] = 3.981071706 x 10 - 6 M Correct amount of sig figs is
found looking at the given values
Round up to 2 sig figs
Given: 0.10 M C 6 H 5 CO 2 Na
[OH - ] = 4.0 x 10 - 6 M
Write Dissociation equation.
Step
4
C H CO - (aq) + H O(l)
6 5 2 2 C H CO H(aq) + OH - (aq)
6 5 2
I 0.10 0 0
C - 4.0 x 10 - 6 + 4.0 x 10 - 6 + 4.0 x 10 - 6
E 0.10 - 4.0 x 10 - 6 4.0 x 10 - 6 4.0 x 10 - 6
[C H CO - ] = 0.099996 ≈ 0.10 M
6 5 2
[C 6 H 5 CO 2 H] = 4.0 x 10 - 6 M
[OH - ] = 4.0 x 10 - 6 M
equilibruium expression
Step
7 Write K b the expression.
[C 6 H 5 CO 2 H][OH - ]
K b =
[C 6 H 5 CO -2]
% ionization pH
[HA] initial % ionization Other ways to say percent ionization
There are two main types of questions you'll see when asked to find the
percent ionization:
Type 1: No ICE Table
Type 2: Requires an ICE Table
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64
Finding Percent Ionization Type 1
pH = 2.16 [H 3 O + ] = 10 - pH
[H O + ] = 10 - 2.16
3
Correct amount of sig figs is
[H O + ] = 0.0069183097 M
3
found looking at the given values
Round up to 2 sig figs
Given: 0.077 M HA
[H 3 O + ] = 0.0069 M
[H 3 O + ] equilibrium
% ionization = x 100
[HA] initial Given in question
0.0069
% ionization = x 100
0.077
% ionization = 8.96103896%
[H + ][NO -2]
K a =
[HNO ] 2
x•x
4.6 x 10 - 4 =
2.4 - x
x2
-
4.6 x 10 =4
2.4 - x
x 2
4.6 x 10 - 4 =
2.4
0.001104 = x 2
0.001104 = x2
0.0332264955 = x
0.0332264955 = x
[H 3 O + ] equilibrium
Use formula: % ionization = x 100.
Step
[HA] initial
6
% ionization = 1.375%
Round up to 2 sig figs
Correct amount of sig figs is
found looking at the given values
% ionization = 1.4%
Given: 2.4 M HNO 2
K a = 4.6 x 10 - 4
9.4%
= 0.094
100
Find [H 3 O + ] by multiplying the decimal to given [HA].
Step
3
[H 3 O + ] = 0.200 x 0.094
[H O + ] = 0.0188 M
3
Round up to 2 sig figs
Correct amount of sig figs is
[H 3 O + ] = 0.019 M found looking at the given values
Find pH using pH = -log [H 3 O + ]. Given: 9.4 %
Step
pH = -log (0.019)
pH = 1.721246399
Round to the correct amount of sig figs.
Step
5
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have
[H 3 O + ] = 0.019 M
[H 3 O + ][A - ]
K a =
[HA]
Solve for K a value by plugging in the equilibrium concentrations
Step
9
into K a expression.
(0.019)(0.019)
K a =
0.181
3.61 x 10 - 4
K a =
0.181
K a = 0.0019944751
Round up to 2 sig figs
K a = 0.0020
pH = 1.72
K a = 0.0020
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71
Using % Ionization to Find Concentration
given
[H +
3 O ] equilibrium
% ionization = x 100
[HA] initial given
[H 3 O + ] equilibrium
13.2% = x 100
0.100
Divide by 100 to both sides.
13.2% = [H O +]
3 equilibrium x 100
100 0.100 100
[H 3 O + ] = 0.0132 M
Note
We ended up with
the correct amount
[BrCH 2 COOH] = 0.0868 M of sig figs, there's
no need to round
[BrCH 2 COO - ] = 0.0132 M
[H 3 O + ] = 0.0132 M
Given the following acids and their associated pK a 's, which is the
strongest acid?
HOOCCl 3 (pK a = 0.7)
H 2 S (pK a = 7.1)
H 3 PO 4 (pK a = 2.1)
HCOOH (pK a = 4.7)
H 2 CO 3 (pK a = 6.4)
a, because pK a the stronger the acid and since 0.7 is the lowest, it is the strongest acid.
Recall K w = K a x K b , this can be applied to pK a and pK b .
pK a + pK b = 14.00
You may be asked to find the pK a from the pK b or vice versa.
pK a + 11.01 = 14.00
Subtract 11.01 from both sides
pK a + 11.01 = 14.00
-11.01 -11.01
pK a = 2.99
Finding pK b from pK a
Plug
Step
1 in pK a into pK a + pK b = 14.00.
3.82 + pK b = 14.00
Subtract 3.82 from both sides
3.82 + pK b = 14.00
-3.82 -3.82
pK b = 10.18
Since K a has 2 sig figs the pK a will Since pK a has 2 decimal places the K a
have 2 decimal places. will have 2 sig figs.
K a = 6.3 x 10 - 5 pK a = 4.200659451 pK a = 3.75 K a = 1.77827941 x 10 - 4
2 sig figs = 2 decimal places 2 decimal places = 2 sig figs
pK a = 4.20 K a = 1.8 x 10 - 4
pK b = 10.66 K b = 7.2 x 10 - 11
L • atm
2
Convert mL to L.
Convert °C to K.
pH = -log (0.00618)
pH = 2.209011525
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 0.00618 M
3 sig figs = 3 decimal places
pH = 2.209011525
Round to 3 decimal places
pH = 2.209
Find [H 3 O + ] using [H 3 O + ] = 10 - pH
Step
2
Step
4 Convert moles of HCl to grams.
588
=
42.444
= 13.8535482 mL
Round to 4 sig figs
13.85 mL
transition metals
Neutral
Composed of a cation of a strong base and the anion of a strong acid.
Example: NaCl
NaOH HCl
is a strong base is a strong acid
Acidic
Composed of a cation of a weak base and the anion of a strong acid.
Example: NH4 Br
NH 3 HBr
is a weak base is a strong acid
Basic
Composed of a cation of a strong base and the anion of a weak acid.
Example: KF
KOH HF
is a strong base is a weak acid
K w = K a (NH 4+ ) x K b (NH 3 )
Recall K w = 1.0 x 10 - 14
K b of NH 3 is found at
1.0 x 10 - 14 = K a (NH 4+ ) x 1.76 x 10 - 5 the end of most
textbooks in the
Divide 1.76 x 10 - 5 to both sides Appendix
1.0 x 10 - 14 = K a (NH 4+ ) x 1.76 x 10 - 5
K b (NH 3 ) = 1.76 x 10 -5
1.76 x 10 - 5 1.76 x 10 - 5
5.68181818 x 10 - 10 = K a (NH 4+ )
Round to 3 sig figs
K a (NH 4+ ) = 5.68 x 10 - 10
K w = K a (HF) x K b (F - )
Recall K w = 1.0 x 10 - 14
K a of HF is found at
1.0 x 10 - 14 = 6.8 x 10 - 4 x K b (F - )
the end of most
Divide 6.8 x 10 - 4 to both sides textbooks in the
Appendix
1.0 x 10 - 14 = 6.8 x 10 - 4 x K b (F - )
6.8 x 10 - 4 6.8 x 10 - 4 K a (HF) = 6.8 x 10 -4
1.47058824 x 10 - 11 = K b (F - )
Round up to 2 sig figs
K b (F - ) = 1.5 x 10 - 11
K a (NH 4+ ) > K b (F - )
Since K a is larger the salt (NH 4 F) is acidic.
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86
Ranking Salts
Rank the relative pH's for solutions of the following
salts, from the lowest pH to highest pH, given the following acidity
data: HCN(K a = 4.9 x 10 - 10 ) HF(Ka = 3.5 x 10 - 4 )
Salts: KCl NH4 Br KCN KF
lowest pH highest pH
(most acidic) (most basic)
cation + + H 2 O base + H 3 O +
Hydrolysis
example: NH 4+ + H 2 O NH 3 + H 3 O + A chemical reaction
where water is added
anion - + H O 2 acid + OH - to break down a
compound.
example: Cl - + H 2 O HCl + OH - If a substance
hydrolyzes it breaks
down.
hydrolysis reactions.
a. AlBr3
Step Dissociation equation: AlBr3 Al 3 + + 3 Br -
1
Step
2
Hydrolysis: Al 3 + + 3 H 2 O Al(OH) 3 + 3 H + Make sure all
equations are
Br - + H 2 O HBr + OH -
balanced
Compare: Al(OH) 3 HBr
Step
acidic
b. C 2 H 5 NH 3 NO 3
Step
1
Dissociation equation: C 2 H 5 NH 3 NO 3 C 2 H 5 NH 3+ + NO 3-
Step
2
Hydrolysis: C 2 H 5 NH 3+ + H 2 O C 2 H 5 NH 2 + H 3 O +
NO 3- + H 2 O HNO 3 + OH -
Compare: C 2 H 5 NH 2
Step
3
HNO 3
weak base strong acid
acidic
Hydrolysis: K + + H 2 O
Step
2 KOH + H +
CO 2 - + H O
3 2 HCO 3- + OH -
Compare: KOH
Step HCO 3-
strong base weak acid
3
basic
d. RbI
Dissociation equation: RbI Rb + + I -
Step
1
Step
2 Hydrolysis: Rb + + H 2 O RbOH + H +
I- + H2O HI + OH -
Compare: RbOH HI
Step
3
neutral
e. NaClO
Step
1 Dissociation equation: NaClO Na + + ClO -
Step
2 Hydrolysis: Na + + H 2 O NaOH + H +
ClO - + H 2 O HClO + OH -
basic
Each type of acid has its own factors for determining acid strength:
Binary Acids (no oxygen)
Bond Polarity and Bond Strength.
electronegativity
If the bond is polar then the structure is acidic
acid strength
nonpolar polar
H C H F
not acidic acidic
6A 7A
The more electronegative the atom attached
to H is, the higher the acid strength.
most electronegative
H2O HF H 2 O HF
acid strength
bond strength
acid strength
H2S HCl
H F H Cl
19.0 35.45
H 2 Te HI
acid strength
Electronegativity of Y
Reason: the more electronegative Y is, the more polar the H-O bond is.
This makes it easier to remove a H + .
HClO 2 HClO 4
O
H O Cl O H O Cl O
1 oxygen
O
3 oxygens
acid strength
electronegativity most
electronegative
acid strength
4A 5A 6A 7A
Factor: CH 3 CH 2 CH 3 CH 3 CH 2 NH 2 CH 3 CH 2 OH CH 3 CH 2 SH
6 7 8 9
C N O F
14 15 16 17
CH
Si P S Cl 3 CH 2 OH > CH 3 CH 2 NH 2 > CH 3 CH 2 SH > CH 3 CH 2 CH 3
32 33 34 35
Ge As Se Br
Cl Cl
Factor: The closer the electronegative atom is to another
electronegative atom the stronger the acid.
CH 3 CH 2 CHCOOH > CH 3 CHCH 2 COOH > ClCH 2 CH 2 CH 2 COOH > CH 3 CH 2 CH 2 COOH
Cl Cl
Write K b expression.
Step
4
equilibruium expression
[HC 2 H 3 O 2 ][OH - ]
K =
b [C 2 H 3 O -2]
K w = K a (HC 2 H 3 O 2 ) x K b (C 2 H 3 O -2)
Recall K w = 1.0 x 10 - 14
1.0 x 10 - 14 = 1.80 x 10 - 5 x K b (C 2 H 3 O -2)
Divide 1.80 x 10 - 5 to both sides
1.0 x 10 - 14 = 1.80 x 10 - 5 x K b (C 2 H 3 O -2)
1.80 x 10 - 5 1.80 x 10 - 5
5.55555556 x 10 - 10 = K b (C 2 H 3 O -2)
Round to 3 sig figs
K (C H O - ) = 5.56 x 10 - 10
b 2 3 2
Step
6 Solve for x.
x2
5.56 x 10 - 10 =
0.250 - x
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95
Finding pH of a Solution with an Anion
Check if the x is small assumption is valid. If valid, apply the
"x is small assumption" by removing the x that is being subtracted.
x2 The 5% rule is valid and x is small
5.56 x 10 - 10 = Clue When K ≤ 10
b
-4
0.250 - x
x2
5.56 x 10 - 10 =
0.250
Multiply the denominator to both sides.
x2
(0.250) x 5.56 x 10 - 10 = x (0.250)
0.250
1.39 x 10 - 10 = x 2
Take the square root of both sides.
1.39 x 10 - 10 = x 2
1.178982612 x 10 - 5 = x
Round to correct amount of sig figs. found looking at the given values
Given: 0.250 M NaC 2 H 3 O 2
[H 3 O + ] = 8.47457627 x 10 - 10 M
K a (HC 2 H 3 O 2 ) = 1.80 x 10 - 5
Round to 3 sig figs
[H O + ] = 8.47 x 10 - 10 M
3
Find pH by using pH = -log [H 3 O + ].
Step
8
pH = -log [8.47 x 10 - 10 ]
pH = 9.07211659
Round to the correct amount of sig figs.
Step
9
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 8.47 x 10 - 10 M
3 sig figs = 3 decimal places
pH = 9.07211659
pH = 9.072
moles of HCl:
150 mL HCl 1 L HCl 0.12 mol HCl
= 0.018 mol HCl
1000 mL HCl 1 L HCl
moles of HCl:
250 mL HNO 3 1 L HNO 3 0.18 mol HNO 3
= 0.045 mol HNO 3
1000 mL HNO 3 1 L HNO 3
400 mL 1L
= 0.4 L
1000 mL
Find [H 3 O + ] by dividing the total moles by the total volume.
Step
5
0.063 mol H 3 O +
[H 3 O ] = +
0.4 L of solution
[H 3 O + ] = 0.1575 M
Plug in new [H 3 O + ] into pH = -log [H 3 O + ]
Step
6
pH = -log (0.1575)
pH = 0.8027194419
Step
7 Round to the correct amount of sig figs.
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
pH = 0.80
[HBr] = 0.115 M
[HBr] = [H O + ]
3
[H 3 O + ] = 0.115 M
Step
4 Write K a expression.
equilibruium expression
[H O + ][CHO - ]
3 2
K a =
[HCHO 2 ]
x2
1.8 x 10 - 4 =
0.125 - x
x 2
1.8 x 10 - 4 =
0.125
2.25 x 10 - 5 = x 2
2.25 x 10 - 5 = x2
0.0047434165 = x
0.0047434165 = x
pH = -log (0.1197)
pH = 0.9219058496
Round to the correct amount of sig figs.
Step
8
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
pH = 0.922
HCN K a = 6.2 x 10 - 10
Step
4
Write K a expression.
equilibruium expression
[H O + ][NO - ]
3 2
K a =
[HNO 2 ]
x2
-
4.0 x 10 =4
5.00 - x
x 2
4.0 x 10 - 4 =
5.00
0.002 = x 2
0.002 = x2
0.0447213595 = x
0.0447213595 = x
The amount of sig figs the concentration has equals the number of decimal places
the pH or pOH will have.
[H 3 O + ] = 0.045 M
2 sig figs = 2 decimal places
pH = 1.346787496
Round up to 2 decimal places
pH = 1.35