Chemical EquilibriumTopic #32 of 40

ICE Tables

Using Initial-Change-Equilibrium tables to solve equilibrium problems.

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

ReactantsProducts
InitialStarting amountsStarting amounts
ChangeHow much changesHow much changes
EquilibriumFinal amountsFinal 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
  • Products: +coefficient×x+\text{coefficient} \times x

Step 4: Write Equilibrium expressions

  • Equilibrium = Initial + Change

Step 5: Substitute into K expression and solve

Example 1: Simple Equilibrium

Problem: For H2(g)+I2(g)2HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\text{HI}(g), Kc=50.5K_c = 50.5 at 448°C Initial: [H2]=[I2]=0.100[\text{H}_2] = [\text{I}_2] = 0.100 M, [HI]=0[\text{HI}] = 0 Find equilibrium concentrations.

ICE Table:

H₂I₂2HI
I0.1000.1000
Cx-xx-x+2x+2x
E0.100x0.100-x0.100x0.100-x2x2x

Solve:

Kc=[HI]2[H2][I2]K_c = \frac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]} 50.5=(2x)2(0.100x)(0.100x)=4x2(0.100x)250.5 = \frac{(2x)^2}{(0.100-x)(0.100-x)} = \frac{4x^2}{(0.100-x)^2}

Take square root:

50.5=2x0.100x\sqrt{50.5} = \frac{2x}{0.100-x} 7.11=2x0.100x7.11 = \frac{2x}{0.100-x} 7.11(0.100x)=2x7.11(0.100-x) = 2x 0.7117.11x=2x0.711 - 7.11x = 2x x=0.078 Mx = 0.078 \text{ M} [H2]=[I2]=0.1000.078=0.022 M[\text{H}_2] = [\text{I}_2] = 0.100 - 0.078 = 0.022 \text{ M} [HI]=2(0.078)=0.156 M[\text{HI}] = 2(0.078) = 0.156 \text{ M}

Example 2: Starting with Products

Problem: For N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\text{NO}_2(g), Kc=4.63×103K_c = 4.63 \times 10^{-3} Initial: [N2O4]=0.100[\text{N}_2\text{O}_4] = 0.100 M Find equilibrium concentrations.

ICE Table:

N₂O₄2NO₂
I0.1000
Cx-x+2x+2x
E0.100x0.100-x2x2x

Solve:

Kc=[NO2]2[N2O4]=(2x)20.100x=4x20.100xK_c = \frac{[\text{NO}_2]^2}{[\text{N}_2\text{O}_4]} = \frac{(2x)^2}{0.100-x} = \frac{4x^2}{0.100-x} 4.63×103=4x20.100x4.63 \times 10^{-3} = \frac{4x^2}{0.100-x}

Using quadratic formula: x=0.00977x = 0.00977 M

[N2O4]=0.1000.00977=0.090 M[\text{N}_2\text{O}_4] = 0.100 - 0.00977 = 0.090 \text{ M} [NO2]=2(0.00977)=0.0195 M[\text{NO}_2] = 2(0.00977) = 0.0195 \text{ M}

Example 3: Using the 5% Approximation

When K is very small, xx \ll initial concentration.

Problem: For HA(aq)H+(aq)+A(aq)\text{HA}(aq) \rightleftharpoons \text{H}^+(aq) + \text{A}^-(aq), Ka=1.8×105K_a = 1.8 \times 10^{-5} Initial: [HA]=0.100[\text{HA}] = 0.100 M

ICE Table:

HAH⁺A⁻
I0.10000
Cx-x+x+x+x+x
E0.100x0.100-xxxxx

Solve with approximation:

Ka=[H+][A][HA]=x20.100xK_a = \frac{[\text{H}^+][\text{A}^-]}{[\text{HA}]} = \frac{x^2}{0.100-x}

Since KaK_a is small, assume x0.100x \ll 0.100:

1.8×105x20.1001.8 \times 10^{-5} \approx \frac{x^2}{0.100} x2=1.8×106x^2 = 1.8 \times 10^{-6} x=1.34×103 Mx = 1.34 \times 10^{-3} \text{ M}

Check approximation:

1.34×1030.100×100%=1.34%\frac{1.34 \times 10^{-3}}{0.100} \times 100\% = 1.34\%

1.34%<5%1.34\% < 5\%, so approximation is valid!

When to Use Approximation

ConditionUse Approximation?
[Initial]/K>100[\text{Initial}]/K > 100Yes
[Initial]/K<100[\text{Initial}]/K < 100No, use quadratic
x/[Initial]<5%x/[\text{Initial}] < 5\%Approximation valid
x/[Initial]>5%x/[\text{Initial}] > 5\%Redo without approximation

Example 4: ICE with Reaction Quotient

Problem: For CO(g)+H2O(g)CO2(g)+H2(g)\text{CO}(g) + \text{H}_2\text{O}(g) \rightleftharpoons \text{CO}_2(g) + \text{H}_2(g), Kc=5.0K_c = 5.0 Initial: All species = 0.10 M Find equilibrium concentrations.

First, find Q:

Q=[CO2][H2][CO][H2O]=(0.10)(0.10)(0.10)(0.10)=1.0Q = \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<KQ < K, so reaction shifts RIGHT

ICE Table:

COH₂OCO₂H₂
I0.100.100.100.10
Cx-xx-x+x+x+x+x
E0.10x0.10-x0.10x0.10-x0.10+x0.10+x0.10+x0.10+x

Solve:

5.0=(0.10+x)2(0.10x)25.0 = \frac{(0.10+x)^2}{(0.10-x)^2} 5.0=0.10+x0.10x\sqrt{5.0} = \frac{0.10+x}{0.10-x} 2.24(0.10x)=0.10+x2.24(0.10-x) = 0.10+x 0.2242.24x=0.10+x0.224 - 2.24x = 0.10 + x 0.124=3.24x0.124 = 3.24x x=0.038 Mx = 0.038 \text{ M} [CO]=[H2O]=0.062 M[\text{CO}] = [\text{H}_2\text{O}] = 0.062 \text{ M} [CO2]=[H2]=0.138 M[\text{CO}_2] = [\text{H}_2] = 0.138 \text{ M}

Common Mistakes to Avoid

  1. Wrong signs for change: Reactants decrease (-), Products increase (++)
  2. Forgetting coefficients: Change = coefficient × xx
  3. Invalid approximation: Always check if x<5%x < 5\% of initial
  4. Wrong direction: Check Q vs K first if not starting from scratch
  5. Negative concentrations: xx cannot exceed initial reactant concentration

Summary Checklist

  1. ☐ Write balanced equation
  2. ☐ Set up ICE table
  3. ☐ Define xx based on stoichiometry
  4. ☐ Write equilibrium expressions
  5. ☐ Substitute into K expression
  6. ☐ Try approximation or use quadratic
  7. ☐ Check approximation validity
  8. ☐ Calculate final concentrations
  9. ☐ Verify by plugging back into K