Overview
ICE tables (Initial-Change-Equilibrium) are a systematic method for solving equilibrium problems. They organize information about concentration changes as a system reaches equilibrium.
ICE Table Structure
Reactants Products I nitialStarting amounts Starting amounts C hangeHow much changes How much changes E quilibriumFinal amounts Final amounts
Setting Up ICE Tables
Step 1: Write the balanced equation
Step 2: Fill in Initial concentrations
Step 3: Express Changes using variable x
Reactants: − coefficient × x -\text{coefficient} \times x − coefficient × x
Products: + coefficient × x +\text{coefficient} \times x + coefficient × x
Step 4: Write Equilibrium expressions
Equilibrium = Initial + Change
Step 5: Substitute into K expression and solve
Example 1: Simple Equilibrium
Problem: For H 2 ( g ) + I 2 ( g ) ⇌ 2 HI ( g ) \text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\text{HI}(g) H 2 ( g ) + I 2 ( g ) ⇌ 2 HI ( g ) , K c = 50.5 K_c = 50.5 K c = 50.5 at 448°C
Initial: [ H 2 ] = [ I 2 ] = 0.100 [\text{H}_2] = [\text{I}_2] = 0.100 [ H 2 ] = [ I 2 ] = 0.100 M, [ HI ] = 0 [\text{HI}] = 0 [ HI ] = 0
Find equilibrium concentrations.
ICE Table:
H₂ I₂ 2HI I 0.100 0.100 0 C − x -x − x − x -x − x + 2 x +2x + 2 x E 0.100 − x 0.100-x 0.100 − x 0.100 − x 0.100-x 0.100 − x 2 x 2x 2 x
Solve:
K c = [ HI ] 2 [ H 2 ] [ I 2 ] K_c = \frac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]} K c = [ H 2 ] [ I 2 ] [ HI ] 2
50.5 = ( 2 x ) 2 ( 0.100 − x ) ( 0.100 − x ) = 4 x 2 ( 0.100 − x ) 2 50.5 = \frac{(2x)^2}{(0.100-x)(0.100-x)} = \frac{4x^2}{(0.100-x)^2} 50.5 = ( 0.100 − x ) ( 0.100 − x ) ( 2 x ) 2 = ( 0.100 − x ) 2 4 x 2
Take square root:
50.5 = 2 x 0.100 − x \sqrt{50.5} = \frac{2x}{0.100-x} 50.5 = 0.100 − x 2 x
7.11 = 2 x 0.100 − x 7.11 = \frac{2x}{0.100-x} 7.11 = 0.100 − x 2 x
7.11 ( 0.100 − x ) = 2 x 7.11(0.100-x) = 2x 7.11 ( 0.100 − x ) = 2 x
0.711 − 7.11 x = 2 x 0.711 - 7.11x = 2x 0.711 − 7.11 x = 2 x
x = 0.078 M x = 0.078 \text{ M} x = 0.078 M
[ H 2 ] = [ I 2 ] = 0.100 − 0.078 = 0.022 M [\text{H}_2] = [\text{I}_2] = 0.100 - 0.078 = 0.022 \text{ M} [ H 2 ] = [ I 2 ] = 0.100 − 0.078 = 0.022 M
[ HI ] = 2 ( 0.078 ) = 0.156 M [\text{HI}] = 2(0.078) = 0.156 \text{ M} [ HI ] = 2 ( 0.078 ) = 0.156 M
Example 2: Starting with Products
Problem: For N 2 O 4 ( g ) ⇌ 2 NO 2 ( g ) \text{N}_2\text{O}_4(g) \rightleftharpoons 2\text{NO}_2(g) N 2 O 4 ( g ) ⇌ 2 NO 2 ( g ) , K c = 4.63 × 10 − 3 K_c = 4.63 \times 10^{-3} K c = 4.63 × 1 0 − 3
Initial: [ N 2 O 4 ] = 0.100 [\text{N}_2\text{O}_4] = 0.100 [ N 2 O 4 ] = 0.100 M
Find equilibrium concentrations.
ICE Table:
N₂O₄ 2NO₂ I 0.100 0 C − x -x − x + 2 x +2x + 2 x E 0.100 − x 0.100-x 0.100 − x 2 x 2x 2 x
Solve:
K c = [ NO 2 ] 2 [ N 2 O 4 ] = ( 2 x ) 2 0.100 − x = 4 x 2 0.100 − x K_c = \frac{[\text{NO}_2]^2}{[\text{N}_2\text{O}_4]} = \frac{(2x)^2}{0.100-x} = \frac{4x^2}{0.100-x} K c = [ N 2 O 4 ] [ NO 2 ] 2 = 0.100 − x ( 2 x ) 2 = 0.100 − x 4 x 2
4.63 × 10 − 3 = 4 x 2 0.100 − x 4.63 \times 10^{-3} = \frac{4x^2}{0.100-x} 4.63 × 1 0 − 3 = 0.100 − x 4 x 2
Using quadratic formula: x = 0.00977 x = 0.00977 x = 0.00977 M
[ N 2 O 4 ] = 0.100 − 0.00977 = 0.090 M [\text{N}_2\text{O}_4] = 0.100 - 0.00977 = 0.090 \text{ M} [ N 2 O 4 ] = 0.100 − 0.00977 = 0.090 M
[ NO 2 ] = 2 ( 0.00977 ) = 0.0195 M [\text{NO}_2] = 2(0.00977) = 0.0195 \text{ M} [ NO 2 ] = 2 ( 0.00977 ) = 0.0195 M
Example 3: Using the 5% Approximation
When K is very small, x ≪ x \ll x ≪ initial concentration.
Problem: For HA ( a q ) ⇌ H + ( a q ) + A − ( a q ) \text{HA}(aq) \rightleftharpoons \text{H}^+(aq) + \text{A}^-(aq) HA ( a q ) ⇌ H + ( a q ) + A − ( a q ) , K a = 1.8 × 10 − 5 K_a = 1.8 \times 10^{-5} K a = 1.8 × 1 0 − 5
Initial: [ HA ] = 0.100 [\text{HA}] = 0.100 [ HA ] = 0.100 M
ICE Table:
HA H⁺ A⁻ I 0.100 0 0 C − x -x − x + x +x + x + x +x + x E 0.100 − x 0.100-x 0.100 − x x x x x x x
Solve with approximation:
K a = [ H + ] [ A − ] [ HA ] = x 2 0.100 − x K_a = \frac{[\text{H}^+][\text{A}^-]}{[\text{HA}]} = \frac{x^2}{0.100-x} K a = [ HA ] [ H + ] [ A − ] = 0.100 − x x 2
Since K a K_a K a is small, assume x ≪ 0.100 x \ll 0.100 x ≪ 0.100 :
1.8 × 10 − 5 ≈ x 2 0.100 1.8 \times 10^{-5} \approx \frac{x^2}{0.100} 1.8 × 1 0 − 5 ≈ 0.100 x 2
x 2 = 1.8 × 10 − 6 x^2 = 1.8 \times 10^{-6} x 2 = 1.8 × 1 0 − 6
x = 1.34 × 10 − 3 M x = 1.34 \times 10^{-3} \text{ M} x = 1.34 × 1 0 − 3 M
Check approximation:
1.34 × 10 − 3 0.100 × 100 % = 1.34 % \frac{1.34 \times 10^{-3}}{0.100} \times 100\% = 1.34\% 0.100 1.34 × 1 0 − 3 × 100% = 1.34%
1.34 % < 5 % 1.34\% < 5\% 1.34% < 5% , so approximation is valid!
When to Use Approximation
Condition Use Approximation? [ Initial ] / K > 100 [\text{Initial}]/K > 100 [ Initial ] / K > 100 Yes [ Initial ] / K < 100 [\text{Initial}]/K < 100 [ Initial ] / K < 100 No, use quadratic x / [ Initial ] < 5 % x/[\text{Initial}] < 5\% x / [ Initial ] < 5% Approximation valid x / [ Initial ] > 5 % x/[\text{Initial}] > 5\% x / [ Initial ] > 5% Redo without approximation
Example 4: ICE with Reaction Quotient
Problem: For CO ( g ) + H 2 O ( g ) ⇌ CO 2 ( g ) + H 2 ( g ) \text{CO}(g) + \text{H}_2\text{O}(g) \rightleftharpoons \text{CO}_2(g) + \text{H}_2(g) CO ( g ) + H 2 O ( g ) ⇌ CO 2 ( g ) + H 2 ( g ) , K c = 5.0 K_c = 5.0 K c = 5.0
Initial: All species = 0.10 M
Find equilibrium concentrations.
First, find Q:
Q = [ CO 2 ] [ H 2 ] [ CO ] [ H 2 O ] = ( 0.10 ) ( 0.10 ) ( 0.10 ) ( 0.10 ) = 1.0 Q = \frac{[\text{CO}_2][\text{H}_2]}{[\text{CO}][\text{H}_2\text{O}]} = \frac{(0.10)(0.10)}{(0.10)(0.10)} = 1.0 Q = [ CO ] [ H 2 O ] [ CO 2 ] [ H 2 ] = ( 0.10 ) ( 0.10 ) ( 0.10 ) ( 0.10 ) = 1.0
Q < K Q < K Q < K , so reaction shifts RIGHT
ICE Table:
CO H₂O CO₂ H₂ I 0.10 0.10 0.10 0.10 C − x -x − x − x -x − x + x +x + x + x +x + x E 0.10 − x 0.10-x 0.10 − x 0.10 − x 0.10-x 0.10 − x 0.10 + x 0.10+x 0.10 + x 0.10 + x 0.10+x 0.10 + x
Solve:
5.0 = ( 0.10 + x ) 2 ( 0.10 − x ) 2 5.0 = \frac{(0.10+x)^2}{(0.10-x)^2} 5.0 = ( 0.10 − x ) 2 ( 0.10 + x ) 2
5.0 = 0.10 + x 0.10 − x \sqrt{5.0} = \frac{0.10+x}{0.10-x} 5.0 = 0.10 − x 0.10 + x
2.24 ( 0.10 − x ) = 0.10 + x 2.24(0.10-x) = 0.10+x 2.24 ( 0.10 − x ) = 0.10 + x
0.224 − 2.24 x = 0.10 + x 0.224 - 2.24x = 0.10 + x 0.224 − 2.24 x = 0.10 + x
0.124 = 3.24 x 0.124 = 3.24x 0.124 = 3.24 x
x = 0.038 M x = 0.038 \text{ M} x = 0.038 M
[ CO ] = [ H 2 O ] = 0.062 M [\text{CO}] = [\text{H}_2\text{O}] = 0.062 \text{ M} [ CO ] = [ H 2 O ] = 0.062 M
[ CO 2 ] = [ H 2 ] = 0.138 M [\text{CO}_2] = [\text{H}_2] = 0.138 \text{ M} [ CO 2 ] = [ H 2 ] = 0.138 M
Common Mistakes to Avoid
Wrong signs for change : Reactants decrease (− - − ), Products increase (+ + + )
Forgetting coefficients : Change = coefficient × x x x
Invalid approximation : Always check if x < 5 % x < 5\% x < 5% of initial
Wrong direction : Check Q vs K first if not starting from scratch
Negative concentrations : x x x cannot exceed initial reactant concentration
Summary Checklist
☐ Write balanced equation
☐ Set up ICE table
☐ Define x x x based on stoichiometry
☐ Write equilibrium expressions
☐ Substitute into K expression
☐ Try approximation or use quadratic
☐ Check approximation validity
☐ Calculate final concentrations
☐ Verify by plugging back into K