🎯⭐ INTERACTIVE LESSON

ICE Tables and Equilibrium Calculations

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ICE Tables and Equilibrium Calculations - Complete Interactive Lesson

Part 1: Setting Up ICE Tables

🧊 Setting Up ICE Tables

Part 1 of 7 — Initial, Change, Equilibrium

ICE tables are the systematic method for solving equilibrium problems. ICE stands for Initial, Change, Equilibrium — the three rows that track how concentrations evolve from start to finish.

The ICE Table Structure

For the reaction: aA+bBcC+dDaA + bB \rightleftharpoons cC + dD

AABBCCDD
I (Initial)[A]0[A]_0[B]0[B]_0[C]0[C]_0[D]0[D]_0
C (Change)ax-axbx-bx+cx+cx+dx+dx
E (Equilibrium)[A]0ax[A]_0 - ax[B]0bx[B]_0 - bx[C]0+cx[C]_0 + cx[D]0+dx[D]_0 + dx

Key Rules

  1. I row: Fill in starting concentrations (often products start at 0)
  2. C row: Use the variable xx with stoichiometric ratios
    • Reactants decrease (negative sign)
    • Products increase (positive sign)
    • Coefficients become multipliers of xx
  3. E row: I + C for each column
  4. Substitute the E row into the KK expression and solve for xx

Important

  • The signs in the C row depend on the direction of shift
  • If the reaction shifts right: reactants lose (-), products gain (++)
  • If the reaction shifts left: reactants gain (++), products lose (-)

Worked Example

H2(g)+I2(g)2HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g), Kc=50.0K_c = 50.0

Initial: [H2]=1.00[\text{H}_2] = 1.00 M, [I2]=1.00[\text{I}_2] = 1.00 M, [HI]=0[\text{HI}] = 0 M

Since we start with no products and K>0K > 0, the reaction shifts right.

H₂I₂2 HI
I1.001.000
Cx-xx-x+2x+2x
E1.00x1.00 - x1.00x1.00 - x2x2x

Substitute into K expression:

Kc=[HI]2[H2][I2]=(2x)2(1.00x)(1.00x)=4x2(1.00x)2K_c = \frac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]} = \frac{(2x)^2}{(1.00 - x)(1.00 - x)} = \frac{4x^2}{(1.00 - x)^2}

50.0=4x2(1.00x)250.0 = \frac{4x^2}{(1.00 - x)^2}

Take the square root of both sides:

50.0=2x1.00x    7.07=2x1.00x\sqrt{50.0} = \frac{2x}{1.00 - x} \implies 7.07 = \frac{2x}{1.00 - x}

7.07(1.00x)=2x    7.077.07x=2x7.07(1.00 - x) = 2x \implies 7.07 - 7.07x = 2x

7.07=9.07x    x=0.7807.07 = 9.07x \implies x = 0.780

Equilibrium concentrations:

  • [H2]=1.000.780=0.220[\text{H}_2] = 1.00 - 0.780 = 0.220 M
  • [I2]=1.000.780=0.220[\text{I}_2] = 1.00 - 0.780 = 0.220 M
  • [HI]=2(0.780)=1.560[\text{HI}] = 2(0.780) = 1.560 M

ICE Table Setup 🎯

ICE Table Setup Practice 🧮

For: N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\,\text{NO}_2(g)

Initial concentrations: [N2O4]=0.50[\text{N}_2\text{O}_4] = 0.50 M, [NO2]=0[\text{NO}_2] = 0 M

  1. If the change in [N2O4][\text{N}_2\text{O}_4] is x-x, what is the change in [NO2][\text{NO}_2]? (Enter with sign, e.g., "+2x")

  2. What is the equilibrium expression for [N2O4][\text{N}_2\text{O}_4] in terms of x? (Enter, e.g., "0.50 - x")

  3. What is the equilibrium expression for [NO2][\text{NO}_2] in terms of x? (Enter, e.g., "2x")

ICE Table Concepts 🔍

Exit Quiz — ICE Table Setup

Part 2: Solving for x

🧊 Solving for K from Equilibrium Data

Part 2 of 7 — When You Know the Equilibrium Concentrations

The simplest ICE table problem: you're given enough information about the equilibrium state to directly calculate K. No algebra needed — just plug and chug.

Method: All Equilibrium Concentrations Given

If you know ALL equilibrium concentrations, just plug them into the K expression.

Example 1

N2(g)+3H2(g)2NH3(g)\text{N}_2(g) + 3\,\text{H}_2(g) \rightleftharpoons 2\,\text{NH}_3(g)

At equilibrium: [N2]=0.50[\text{N}_2] = 0.50, [H2]=0.30[\text{H}_2] = 0.30, [NH3]=0.20[\text{NH}_3] = 0.20 M

Kc=[NH3]2[N2][H2]3=(0.20)2(0.50)(0.30)3=0.040(0.50)(0.027)=0.0400.0135=2.963.0K_c = \frac{[\text{NH}_3]^2}{[\text{N}_2][\text{H}_2]^3} = \frac{(0.20)^2}{(0.50)(0.30)^3} = \frac{0.040}{(0.50)(0.027)} = \frac{0.040}{0.0135} = 2.96 \approx 3.0

Method: Initial + One Equilibrium Value Given

When you know initial concentrations and ONE equilibrium concentration, use the ICE table to find x, then calculate all equilibrium concentrations.

Example 2

PCl5(g)PCl3(g)+Cl2(g)\text{PCl}_5(g) \rightleftharpoons \text{PCl}_3(g) + \text{Cl}_2(g)

Initial: [PCl5]=1.00[\text{PCl}_5] = 1.00 M, [PCl3]=[Cl2]=0[\text{PCl}_3] = [\text{Cl}_2] = 0

At equilibrium: [PCl5]=0.60[\text{PCl}_5] = 0.60 M

PCl₅PCl₃Cl₂
I1.0000
Cx-x+x+x+x+x
E1.00x1.00 - xxxxx

From the equilibrium value: 1.00x=0.60    x=0.401.00 - x = 0.60 \implies x = 0.40

So: [PCl3]=[Cl2]=0.40[\text{PCl}_3] = [\text{Cl}_2] = 0.40 M

Kc=(0.40)(0.40)0.60=0.160.60=0.2670.27K_c = \frac{(0.40)(0.40)}{0.60} = \frac{0.16}{0.60} = 0.267 \approx 0.27

Finding K 🎯

Practice Problem 1 🧮

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)

At equilibrium: [CO]=0.10[\text{CO}] = 0.10, [H2O]=0.10[\text{H}_2\text{O}] = 0.10, [CO2]=0.30[\text{CO}_2] = 0.30, [H2]=0.30[\text{H}_2] = 0.30 M

  1. Calculate KcK_c. (Enter as a whole number)

  2. Is this reaction product-favored or reactant-favored? (Enter "product-favored" or "reactant-favored")

Practice Problem 2 🧮

N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\,\text{NO}_2(g)

Initial: [N2O4]=0.80[\text{N}_2\text{O}_4] = 0.80 M, [NO2]=0[\text{NO}_2] = 0 M

At equilibrium: [NO2]=0.40[\text{NO}_2] = 0.40 M

  1. What is xx? (Enter as a decimal)

  2. What is [N2O4][\text{N}_2\text{O}_4] at equilibrium? (Enter as a decimal)

  3. Calculate KcK_c. (Enter to 3 significant figures)

Solving for K — Concepts 🔍

Exit Quiz — Solving for K

Part 3: Small-x Approximation

🧊 Solving for Equilibrium Concentrations Given K

Part 3 of 7 — The Classic ICE Table Problem

This is the most common ICE table scenario: you know K and the initial concentrations, and you need to find the equilibrium concentrations. This requires setting up and solving an algebraic equation.

General Method

  1. Write the balanced equation and KK expression
  2. Set up the ICE table with initial concentrations
  3. Determine the direction of shift (usually Q=0<KQ = 0 < K, so shift right)
  4. Express equilibrium concentrations in terms of xx
  5. Substitute into the KK expression
  6. Solve for xx
  7. Calculate all equilibrium concentrations
  8. Check: plug values back into K to verify

Perfect-Square Shortcut

When the K expression can be written as a perfect square, take the square root of both sides to avoid the quadratic formula.

This works when: K=(something)2(something else)2K = \frac{(\text{something})^2}{(\text{something else})^2}

Worked Example: Perfect-Square Case

H2(g)+I2(g)2HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g), Kc=64.0K_c = 64.0

Initial: [H2]=0.50[\text{H}_2] = 0.50 M, [I2]=0.50[\text{I}_2] = 0.50 M, [HI]=0[\text{HI}] = 0

H₂I₂HI
I0.500.500
Cx-xx-x+2x+2x
E0.50x0.50-x0.50x0.50-x2x2x

64.0=(2x)2(0.50x)(0.50x)=4x2(0.50x)264.0 = \frac{(2x)^2}{(0.50-x)(0.50-x)} = \frac{4x^2}{(0.50-x)^2}

Take the square root:

8.0=2x0.50x8.0 = \frac{2x}{0.50-x}

8.0(0.50x)=2x    4.08.0x=2x    4.0=10.0x8.0(0.50 - x) = 2x \implies 4.0 - 8.0x = 2x \implies 4.0 = 10.0x

x=0.40x = 0.40

Equilibrium concentrations:

  • [H2]=[I2]=0.500.40=0.10[\text{H}_2] = [\text{I}_2] = 0.50 - 0.40 = 0.10 M
  • [HI]=2(0.40)=0.80[\text{HI}] = 2(0.40) = 0.80 M

Check: K=(0.80)2(0.10)(0.10)=0.640.01=64.0K = \frac{(0.80)^2}{(0.10)(0.10)} = \frac{0.64}{0.01} = 64.0

Worked Example: Quadratic Required

N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\,\text{NO}_2(g), Kc=0.36K_c = 0.36

Initial: [N2O4]=1.00[\text{N}_2\text{O}_4] = 1.00 M, [NO2]=0[\text{NO}_2] = 0

N₂O₄NO₂
I1.000
Cx-x+2x+2x
E1.00x1.00 - x2x2x

0.36=(2x)21.00x=4x21.00x0.36 = \frac{(2x)^2}{1.00 - x} = \frac{4x^2}{1.00 - x}

0.36(1.00x)=4x20.36(1.00 - x) = 4x^2

0.360.36x=4x20.36 - 0.36x = 4x^2

4x2+0.36x0.36=04x^2 + 0.36x - 0.36 = 0

Using the quadratic formula: x=0.36±(0.36)2+4(4)(0.36)2(4)x = \frac{-0.36 \pm \sqrt{(0.36)^2 + 4(4)(0.36)}}{2(4)}

x=0.36±0.1296+5.768=0.36±5.88968=0.36±2.4278x = \frac{-0.36 \pm \sqrt{0.1296 + 5.76}}{8} = \frac{-0.36 \pm \sqrt{5.8896}}{8} = \frac{-0.36 \pm 2.427}{8}

Taking the positive root: x=0.36+2.4278=2.0678=0.258x = \frac{-0.36 + 2.427}{8} = \frac{2.067}{8} = 0.258

Equilibrium: [N2O4]=0.742[\text{N}_2\text{O}_4] = 0.742 M, [NO2]=0.516[\text{NO}_2] = 0.516 M

Setting Up the Algebra 🎯

Practice: Solve an ICE Table 🧮

A(g)B(g)+C(g)\text{A}(g) \rightleftharpoons \text{B}(g) + \text{C}(g), Kc=0.25K_c = 0.25

Initial: [A]=1.00[\text{A}] = 1.00 M, [B]=[C]=0[\text{B}] = [\text{C}] = 0

ABC
I1.0000
Cx-x+x+x+x+x
E1.00x1.00-xxxxx

0.25=xx1.00x=x21.00x0.25 = \frac{x \cdot x}{1.00 - x} = \frac{x^2}{1.00 - x}

  1. Rearrange to standard quadratic form: x2+0.25x0.25=0x^2 + 0.25x - 0.25 = 0. Using the quadratic formula, x=?x = ? (Round to 3 significant figures)

  2. What is [A][\text{A}] at equilibrium? (Round to 3 significant figures)

  3. What is [B][\text{B}] at equilibrium? (Round to 3 significant figures)

Problem-Solving Strategy 🔍

Exit Quiz — Solving for Equilibrium Concentrations

Part 4: Quadratic Solutions

🧊 The 5% Approximation

Part 4 of 7 — When x Is Small Enough to Ignore

When K is very small (K<103K < 10^{-3}) relative to initial concentrations, the change xx is often negligible compared to the initial values. This allows us to simplify the algebra dramatically.

When Can You Use the Approximation?

The Rule of Thumb

If [initial]K>100\frac{[\text{initial}]}{K} > 100 (or equivalently, K<0.01×[initial]K < 0.01 \times [\text{initial}]), then xx is small enough to approximate:

[initial]x[initial][\text{initial}] - x \approx [\text{initial}]

Why This Works

When K is very small, the reaction barely shifts — very little product forms. So xx is tiny compared to the initial concentration, and subtracting it doesn't meaningfully change the value.

The 5% Test

After solving, check: x[initial]×100%<5%\frac{x}{[\text{initial}]} \times 100\% < 5\%

If the change is less than 5% of the initial concentration, the approximation is valid.

Worked Example

N2(g)+O2(g)2NO(g)\text{N}_2(g) + \text{O}_2(g) \rightleftharpoons 2\,\text{NO}(g), Kc=4.0×104K_c = 4.0 \times 10^{-4}

Initial: [N2]=0.80[\text{N}_2] = 0.80 M, [O2]=0.20[\text{O}_2] = 0.20 M, [NO]=0[\text{NO}] = 0

Check: 0.20/(4.0×104)=500>1000.20 / (4.0 \times 10^{-4}) = 500 > 100 ✓ → approximation valid

N₂O₂NO
I0.800.200
Cx-xx-x+2x+2x
E0.80x0.80 - x0.20x0.20 - x2x2x

Kc=(2x)2(0.80x)(0.20x)K_c = \frac{(2x)^2}{(0.80 - x)(0.20 - x)}

With approximation (x0.20x \ll 0.20):

4.0×104=4x2(0.80)(0.20)=4x20.164.0 \times 10^{-4} = \frac{4x^2}{(0.80)(0.20)} = \frac{4x^2}{0.16}

4x2=(4.0×104)(0.16)=6.4×1054x^2 = (4.0 \times 10^{-4})(0.16) = 6.4 \times 10^{-5}

x2=1.6×105    x=4.0×103x^2 = 1.6 \times 10^{-5} \implies x = 4.0 \times 10^{-3}

5% Check: x0.20×100%=4.0×1030.20×100%=2.0%\frac{x}{0.20} \times 100\% = \frac{4.0 \times 10^{-3}}{0.20} \times 100\% = 2.0\% ✓ (< 5%)

Equilibrium:

  • [NO]=2(4.0×103)=8.0×103[\text{NO}] = 2(4.0 \times 10^{-3}) = 8.0 \times 10^{-3} M
  • [N2]0.80[\text{N}_2] \approx 0.80 M
  • [O2]0.20[\text{O}_2] \approx 0.20 M

The 5% Approximation 🎯

Practice: Using the Approximation 🧮

A(g)B(g)+C(g)\text{A}(g) \rightleftharpoons \text{B}(g) + \text{C}(g), Kc=1.0×106K_c = 1.0 \times 10^{-6}

Initial: [A]=0.50[\text{A}] = 0.50 M, [B]=[C]=0[\text{B}] = [\text{C}] = 0

Using the approximation 0.50x0.500.50 - x \approx 0.50:

1.0×106=x20.501.0 \times 10^{-6} = \frac{x^2}{0.50}

  1. Solve for xx. (Enter in scientific notation, e.g. 7.1e-4)

  2. What percent of the initial [A] is xx? (Enter as a percentage to 3 significant figures, e.g. 0.14)

  3. Is the approximation valid? (Enter "yes" or "no")

Approximation Guidelines 🔍

Exit Quiz — 5% Approximation

Part 5: ICE Tables with Kp

🧊 When the Approximation Fails — The Quadratic Formula

Part 5 of 7 — Exact Solutions

When K is not small enough for the 5% approximation, or when the 5% test fails, you must solve the full quadratic equation. This part covers the systematic approach.

The Quadratic Formula

For ax2+bx+c=0ax^2 + bx + c = 0:

x=b±b24ac2ax = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}

In Equilibrium Problems

  • You'll always get two solutions
  • Only the positive root that gives physically meaningful (non-negative) concentrations is valid
  • Reject any root that gives a negative concentration

When You Need the Quadratic

The approximation fails when:

  • KK is not very small relative to initial concentrations
  • [initial]K<100\frac{[\text{initial}]}{K} < 100
  • The 5% check yields > 5%

Worked Example

A(g)B(g)+C(g)\text{A}(g) \rightleftharpoons \text{B}(g) + \text{C}(g), Kc=0.50K_c = 0.50

Initial: [A]=1.00[\text{A}] = 1.00 M, [B]=[C]=0[\text{B}] = [\text{C}] = 0

Check approximation: 1.00/0.50=2.0<1001.00/0.50 = 2.0 < 100 → approximation NOT valid

ABC
I1.0000
Cx-x+x+x+x+x
E1.00x1.00-xxxxx

0.50=x21.00x0.50 = \frac{x^2}{1.00 - x}

0.50(1.00x)=x20.50(1.00 - x) = x^2

0.500.50x=x20.50 - 0.50x = x^2

x2+0.50x0.50=0x^2 + 0.50x - 0.50 = 0

Applying the quadratic formula (a=1,b=0.50,c=0.50a = 1, b = 0.50, c = -0.50):

x=0.50±(0.50)24(1)(0.50)2(1)=0.50±0.25+2.002x = \frac{-0.50 \pm \sqrt{(0.50)^2 - 4(1)(-0.50)}}{2(1)} = \frac{-0.50 \pm \sqrt{0.25 + 2.00}}{2}

x=0.50±2.252=0.50±1.502x = \frac{-0.50 \pm \sqrt{2.25}}{2} = \frac{-0.50 \pm 1.50}{2}

Two roots:

  • x=0.50+1.502=1.002=0.50x = \frac{-0.50 + 1.50}{2} = \frac{1.00}{2} = 0.50
  • x=0.501.502=2.002=1.00x = \frac{-0.50 - 1.50}{2} = \frac{-2.00}{2} = -1.00 ✗ (negative)

x=0.50x = 0.50

Equilibrium: [A]=0.50[\text{A}] = 0.50 M, [B]=[C]=0.50[\text{B}] = [\text{C}] = 0.50 M

Check: K=(0.50)(0.50)/0.50=0.50K = (0.50)(0.50)/0.50 = 0.50

Note: If we had used the approximation: x=0.50=0.71x = \sqrt{0.50} = 0.71. The 5% check: 0.71/1.00=71%0.71/1.00 = 71\% → fails badly!

Quadratic Approach 🎯

Practice: Full Quadratic 🧮

N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\,\text{NO}_2(g), Kc=0.36K_c = 0.36

Initial: [N2O4]=0.50[\text{N}_2\text{O}_4] = 0.50 M, [NO2]=0[\text{NO}_2] = 0

The equation is: 4x2+0.36x0.18=04x^2 + 0.36x - 0.18 = 0

Using the quadratic formula:

  1. What is the discriminant b24acb^2 - 4ac? (Enter to 3 significant figures)

  2. What is xx? (Round to 3 significant figures)

  3. What is [NO2][\text{NO}_2] at equilibrium? (Round to 3 significant figures)

Quadratic vs Approximation 🔍

Exit Quiz — Quadratic Formula

Part 6: Problem-Solving Workshop

🧮 Problem-Solving Workshop: ICE Tables

Part 6 of 7 — Multiple ICE Table Scenarios

This workshop presents varied ICE table problems: finding K, finding equilibrium concentrations, using the approximation, and the quadratic. Practice the decision-making process for each type.

Decision Tree for ICE Table Problems

Step 1: What are you solving for?

  • K unknown: Use given equilibrium data to find K
  • Equilibrium concentrations unknown: Use K and initial data to find concentrations

Step 2: Can you use the approximation?

  • Check: [initial]K>100\frac{[\text{initial}]}{K} > 100?
    • Yes → Approximate: [initial]x[initial][\text{initial}] - x \approx [\text{initial}]
    • No → Full quadratic required

Step 3: Solve and verify

  • Solve for xx
  • Calculate all equilibrium concentrations
  • Verify: plug back into K expression
  • If approximation used: check 5% test

Common Patterns

PatternExample
Perfect square(2x)2(ax)2\frac{(2x)^2}{(a-x)^2} → take square root
Small K with approxK=x2aK = \frac{x^2}{a}x=Kax = \sqrt{Ka}
Full quadraticax2+bx+c=0ax^2 + bx + c = 0 → quadratic formula

Problem 1: Finding K 🧮

2HI(g)H2(g)+I2(g)2\,\text{HI}(g) \rightleftharpoons \text{H}_2(g) + \text{I}_2(g)

Initial: [HI]=1.00[\text{HI}] = 1.00 M, [H2]=[I2]=0[\text{H}_2] = [\text{I}_2] = 0

At equilibrium: [HI]=0.80[\text{HI}] = 0.80 M

  1. What is xx? (Remember: the coefficient of HI is 2)

  2. What is [H2][\text{H}_2] at equilibrium?

  3. What is KcK_c? (Enter to 3 significant figures)

Problem 2: Using the Approximation 🧮

COCl2(g)CO(g)+Cl2(g)\text{COCl}_2(g) \rightleftharpoons \text{CO}(g) + \text{Cl}_2(g), Kc=2.2×1010K_c = 2.2 \times 10^{-10}

Initial: [COCl2]=0.50[\text{COCl}_2] = 0.50 M, [CO]=[Cl2]=0[\text{CO}] = [\text{Cl}_2] = 0

Using the approximation 0.50x0.500.50 - x \approx 0.50:

  1. Solve: x=Kc×0.50x = \sqrt{K_c \times 0.50}. What is xx? (Enter in scientific notation, e.g. 1.0e-5)

  2. Does the 5% test pass? (Enter "yes" or "no")

  3. What is [CO][\text{CO}] at equilibrium? (Enter in scientific notation, same as x)

Round all answers to 3 significant figures.

Problem 3: Which Method? 🎯

Problem 4: Non-Zero Initial Products 🧮

H2(g)+I2(g)2HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g), Kc=64K_c = 64

Initial: [H2]=0.50[\text{H}_2] = 0.50, [I2]=0.50[\text{I}_2] = 0.50, [HI]=0.20[\text{HI}] = 0.20 M

First check: Q=(0.20)2(0.50)(0.50)=0.040.25=0.16Q = \frac{(0.20)^2}{(0.50)(0.50)} = \frac{0.04}{0.25} = 0.16. Since Q<KQ < K, shift right.

  1. Using the ICE table with shift right, what is [HI][\text{HI}] at equilibrium expressed in terms of xx? (Enter, e.g., "0.20 + 2x")

  2. This is a perfect-square case. Taking the square root: 8=0.20+2x0.50x8 = \frac{0.20 + 2x}{0.50 - x}. Solve for x. (Round to 3 significant figures)

  3. What is [HI][\text{HI}] at equilibrium? (Round to 3 significant figures)

Exit Quiz — ICE Table Workshop

Part 7: Synthesis & AP Review

🎓 Synthesis & AP Review

Part 7 of 7 — ICE Tables and Equilibrium Calculations

This final part reviews all ICE table techniques: setup, solving for K, solving for concentrations, the 5% approximation, and the quadratic formula. These questions mirror AP Chemistry exam formats.

Complete ICE Table Summary

The ICE Table

ReactantProduct
IInitial concentrationInitial concentration (often 0)
C(-(coeff)(x))(x)+(+(coeff)(x))(x)
EI + CI + C

Problem Types

GivenFindMethod
All equilibrium conc.KPlug directly into K expression
Initial + one eq. conc.KFind x from ICE, then all eq. conc., then K
K + initial conc.Eq. conc.Full ICE → solve for x

Solving Strategies

ConditionStrategy
Perfect squareTake square root
[init]/K>100[\text{init}]/K > 100Small-x approximation
[init]/K<100[\text{init}]/K < 100Full quadratic
Approx gives > 5%Switch to quadratic

Verification

Always check: Plug equilibrium concentrations back into K expression. The calculated K should match the given K.

AP-Style Multiple Choice — Set 1 🎯

AP Free-Response Style 🧮

CO(g)+Cl2(g)COCl2(g)\text{CO}(g) + \text{Cl}_2(g) \rightleftharpoons \text{COCl}_2(g), Kc=255K_c = 255 at 100°C

A 1.00 L flask is charged with 0.400 mol CO and 0.400 mol Cl₂. No COCl₂ is initially present.

  1. Write the K expression and set up the ICE table. What is [COCl2][\text{COCl}_2] at equilibrium in terms of x? (Enter, e.g., "x")

  2. The K expression becomes 255=x(0.400x)2255 = \frac{x}{(0.400-x)^2}. Using the approximation (0.400/2550.400/255 is small... actually 0.400/255=0.00157<1000.400/255 = 0.00157 < 100). Should you use the quadratic? (Enter "yes" or "no")

  3. Actually, [init]/K=0.400/255=0.00157[\text{init}]/K = 0.400/255 = 0.00157, which is much LESS than 100. This means K is LARGE relative to the initial concentration, meaning the reaction goes nearly to completion. The limiting approach here is to assume the reaction goes to completion, then back-calculate. If the reaction goes to completion, what is the limiting reagent amount of COCl₂ formed? (Enter in mol)

Round all answers to 3 significant figures.

Final Concept Review 🔍

Final Exit Quiz