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๐ŸŽฏโญ INTERACTIVE LESSON

ICE Tables and Equilibrium Calculations

Learn step-by-step with interactive practice!

ICE Tables and Equilibrium Calculations - Complete Interactive Lesson

Part 1: Setting Up ICE Tables

๐ŸงŠ Setting Up ICE Tables

Part 1 of 7 โ€” Initial, Change, Equilibrium


Topics in This Part

Section
๐Ÿ—๏ธ The ICE Table Structure
๐Ÿงช Worked Example
Substitute into K expression:

๐Ÿ”‘ Key Concept: Mastering this material will strengthen your foundation for both the AP Chemistry exam and more advanced chemistry topics.


What You'll Master in Part 1

  • Understanding the core concepts covered in Part 1
  • Applying these ideas to solve practice problems
  • Building toward AP exam readiness for this topic

๐Ÿ—๏ธ The ICE Table Structure

For the reaction: aA+bBโ‡ŒcC+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)โˆ’ax-axโˆ’bx-bx+cx+cx+dx+dx
E (Equilibrium)[A]0โˆ’ax[A]_0 - ax[B]0โˆ’bx[B]_0 - bx[C]0+cx[C]_0 + cx[D]0+dx[D]_0 + dx

๐Ÿ”‘ Key Rules:

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

โš ๏ธ Warning: The signs in the C row depend on the direction of shift:

  • If the reaction shifts right: reactants lose (โˆ’-), products gain (++)
  • If the reaction shifts left: reactants gain (++), products lose (โˆ’-)

๐Ÿ’ก Tip: When products start at 0, their equilibrium expressions simplify to just the stoichiometric coefficient times xx (e.g., 0+2x=2x0 + 2x = 2x).

๐Ÿงช Worked Example

Problem: For H2(g)+I2(g)โ‡Œ2โ€‰HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g) with Kc=50.0K_c = 50.0, find the equilibrium concentrations given [H2]=1.00[\text{H}_2] = 1.00 M, [I2]=1.00[\text{I}_2] = 1.00 M, [HI]=0[\text{HI}] = 0 M.

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

H2H_{2}I2I_{2}2 HI
I1.001.000
Cโˆ’x-xโˆ’x-x+2x+2x
E1.00โˆ’x1.00 - x1.00โˆ’x1.00 - x2x2x

Substitute into K expression:

Kc=[HI]2[H2][I2]=(2x)2(1.00โˆ’x)(1.00โˆ’x)=4x2(1.00โˆ’x)2\boxed{K_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(1.00โˆ’x)250.0 = \frac{4x^2}{(1.00 - x)^2}

Take the square root of both sides:

50.0=2x1.00โˆ’xโ€…โ€ŠโŸนโ€…โ€Š7.07=2x1.00โˆ’x\sqrt{50.0} = \frac{2x}{1.00 - x} \implies 7.07 = \frac{2x}{1.00 - x}

7.07(1.00โˆ’x)=2xโ€…โ€ŠโŸนโ€…โ€Š7.07โˆ’7.07x=2x7.07(1.00 - x) = 2x \implies 7.07 - 7.07x = 2x

7.07=9.07xโ€…โ€ŠโŸนโ€…โ€Šx=0.7807.07 = 9.07x \implies x = 0.780

Equilibrium concentrations:

  • [H2]=1.00โˆ’0.780=0.220[\text{H}_2] = 1.00 - 0.780 = 0.220 M
  • [I2]=1.00โˆ’0.780=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 ๐ŸŽฏ

ICE Table Setup Practice ๐Ÿงฎ

For: N2O4(g)โ‡Œ2โ€‰NO2(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 โˆ’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 ๐Ÿ”

Exit Quiz โ€” ICE Table Setup โœ…

Part 2: Solving for x

๐ŸงŠ Solving for K from Equilibrium Data

Part 2 of 7 โ€” When You Know the Equilibrium Concentrations


Topics in This Part

Section
โš–๏ธ Method: All Equilibrium Concentrations Given
Example 1
โš–๏ธ Method: Initial + One Equilibrium Value Given
Example 2

๐Ÿ”‘ Key Concept: Mastering this material will strengthen your foundation for both the AP Chemistry exam and more advanced chemistry topics.


What You'll Master in Part 2

  • Understanding the core concepts covered in Part 2
  • Applying these ideas to solve practice problems
  • Building toward AP exam readiness for this topic

โš–๏ธ Method: All Equilibrium Concentrations Given

๐Ÿ”‘ Key Concept: If you know ALL equilibrium concentrations, just plug them into the K expression.


Example 1

Problem: For N2(g)+3โ€‰H2(g)โ‡Œ2โ€‰NH3(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. Find KcK_c.

Solution:

Kc=[NH3]2[N2][H2]3=(0.20)2(0.50)(0.30)3=0.040(0.50)(0.027)=0.0400.0135=2.96โ‰ˆ3.0\boxed{K_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

โš–๏ธ Method: Initial + One Equilibrium Value Given

๐Ÿ’ก Tip: When you know initial concentrations and ONE equilibrium concentration, use the ICE table to find x, then calculate all equilibrium concentrations.


Example 2

Problem: For PCl5(g)โ‡ŒPCl3(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. Find KcK_c.

Solution:

PCl5PCl_{5}PCl3PCl_{3}Cl2Cl_{2}
I1.0000
Cโˆ’x-x+x+x+x+x
E1.00โˆ’x1.00 - xxxxx

From the equilibrium value: 1.00โˆ’x=0.60โ€…โ€ŠโŸนโ€…โ€Šx=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=0.267โ‰ˆ0.27\boxed{K_c = \frac{(0.40)(0.40)}{0.60}} = \frac{0.16}{0.60} = 0.267 \approx 0.27


โš ๏ธ Warning: When finding xx from a change with a stoichiometric coefficient, remember to divide: if 2x=0.402x = 0.40, then x=0.20x = 0.20, not 0.400.40.

Finding K ๐ŸŽฏ

Practice Problem 1 ๐Ÿงฎ

CO(g)+H2O(g)โ‡ŒCO2(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 ๐Ÿงฎ

N2O4(g)โ‡Œ2โ€‰NO2(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 โ€” Concepts ๐Ÿ”

Exit Quiz โ€” Solving for K โœ…

Part 3: Small-x Approximation

๐ŸงŠ Solving for Equilibrium Concentrations Given K

Part 3 of 7 โ€” The Classic ICE Table Problem


Topics in This Part

Section
๐Ÿ“Œ General Method
๐Ÿงช Worked Example: Perfect-Square Case
๐Ÿงช Worked Example: Quadratic Required

๐Ÿ”‘ Key Concept: Mastering this material will strengthen your foundation for both the AP Chemistry exam and more advanced chemistry topics.


What You'll Master in Part 3

  • Understanding the core concepts covered in Part 3
  • Applying these ideas to solve practice problems
  • Building toward AP exam readiness for this topic

๐Ÿ“Œ 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

๐Ÿ’ก Tip โ€” 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(somethingย else)2K = \frac{(\text{something})^2}{(\text{something else})^2}


๐Ÿ”‘ Key Concept: Always verify your answer โ€” plug the equilibrium concentrations back into the K expression. If the result doesn't match the given K, recheck your algebra.

๐Ÿงช Worked Example: Perfect-Square Case

Problem: For H2(g)+I2(g)โ‡Œ2โ€‰HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g) with Kc=64.0K_c = 64.0, find the equilibrium concentrations given [H2]=0.50[\text{H}_2] = 0.50 M, [I2]=0.50[\text{I}_2] = 0.50 M, [HI]=0[\text{HI}] = 0.

Solution:

H2H_{2}I2I_{2}HI
I0.500.500
Cโˆ’x-xโˆ’x-x+2x+2x
E0.50โˆ’x0.50-x0.50โˆ’x0.50-x2x2x

64.0=(2x)2(0.50โˆ’x)(0.50โˆ’x)=4x2(0.50โˆ’x)2\boxed{64.0 = \frac{(2x)^2}{(0.50-x)(0.50-x)} = \frac{4x^2}{(0.50-x)^2}}

Take the square root:

8.0=2x0.50โˆ’x8.0 = \frac{2x}{0.50-x}

8.0(0.50โˆ’x)=2xโ€…โ€ŠโŸนโ€…โ€Š4.0โˆ’8.0x=2xโ€…โ€ŠโŸนโ€…โ€Š4.0=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]=0.50โˆ’0.40=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 โœ“

๐Ÿงช Worked Example: Quadratic Required

Problem: For N2O4(g)โ‡Œ2โ€‰NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\,\text{NO}_2(g) with Kc=0.36K_c = 0.36, find the equilibrium concentrations given [N2O4]=1.00[\text{N}_2\text{O}_4] = 1.00 M, [NO2]=0[\text{NO}_2] = 0.

Solution:

N2O4N_{2}O_{4}NO2NO_{2}
I1.000
Cโˆ’x-x+2x+2x
E1.00โˆ’x1.00 - x2x2x

0.36=(2x)21.00โˆ’x=4x21.00โˆ’x\boxed{0.36 = \frac{(2x)^2}{1.00 - x} = \frac{4x^2}{1.00 - x}}

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

0.36โˆ’0.36x=4x20.36 - 0.36x = 4x^2

4x2+0.36xโˆ’0.36=04x^2 + 0.36x - 0.36 = 0

Using the quadratic formula: x=โˆ’0.36ยฑ(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=โˆ’0.36ยฑ0.1296+5.768=โˆ’0.36ยฑ5.88968=โˆ’0.36ยฑ2.4278x = \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=โˆ’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


โš ๏ธ Warning: Always reject the negative root of the quadratic โ€” it would give physically impossible (negative) concentrations.

Setting Up the Algebra ๐ŸŽฏ

Practice: Solve an ICE Table ๐Ÿงฎ

A(g)โ‡ŒB(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
Cโˆ’x-x+x+x+x+x
E1.00โˆ’x1.00-xxxxx

0.25=xโ‹…x1.00โˆ’x=x21.00โˆ’x0.25 = \frac{x \cdot x}{1.00 - x} = \frac{x^2}{1.00 - x}

1) Rearrange to standard quadratic form: x2+0.25xโˆ’0.25=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 ๐Ÿ”

Exit Quiz โ€” Solving for Equilibrium Concentrations โœ…

Part 4: Quadratic Solutions

๐ŸงŠ The 5% Approximation

Part 4 of 7 โ€” When x Is Small Enough to Ignore


Topics in This Part

Section
๐Ÿ“Œ When Can You Use the Approximation?
Why This Works
๐Ÿงช Worked Example

๐Ÿ”‘ Key Concept: Mastering this material will strengthen your foundation for both the AP Chemistry exam and more advanced chemistry topics.


What You'll Master in Part 4

  • Understanding the core concepts covered in Part 4
  • Applying these ideas to solve practice problems
  • Building toward AP exam readiness for this topic

๐Ÿ“Œ When Can You Use the Approximation?

๐Ÿ’ก Tip โ€” Rule of Thumb: If [initial]K>100\frac{[\text{initial}]}{K} > 100 (or equivalently, K<0.01ร—[initial]K < 0.01 \times [\text{initial}]), then xx is small enough to approximate:

[initial]โˆ’xโ‰ˆ[initial]\boxed{[\text{initial}] - x \approx [\text{initial}]}


Why This Works

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


๐Ÿ”‘ The 5% Test: After solving, check:

x[initial]ร—100%<5%\boxed{\frac{x}{[\text{initial}]} \times 100\% < 5\%}

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


โš ๏ธ Warning: If the 5% test fails (change > 5%), your approximated answer is inaccurate. Discard it and solve the full quadratic equation instead.

๐Ÿงช Worked Example

Problem: For N2(g)+O2(g)โ‡Œ2โ€‰NO(g)\text{N}_2(g) + \text{O}_2(g) \rightleftharpoons 2\,\text{NO}(g) with Kc=4.0ร—10โˆ’4K_c = 4.0 \times 10^{-4}, find the equilibrium concentrations given [N2]=0.80[\text{N}_2] = 0.80 M, [O2]=0.20[\text{O}_2] = 0.20 M, [NO]=0[\text{NO}] = 0.

Solution: Check: 0.20/(4.0ร—10โˆ’4)=500>1000.20 / (4.0 \times 10^{-4}) = 500 > 100 โœ“ โ†’ approximation valid

N2N_{2}O2O_{2}NO
I0.800.200
Cโˆ’x-xโˆ’x-x+2x+2x
E0.80โˆ’x0.80 - x0.20โˆ’x0.20 - x2x2x

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

With approximation (xโ‰ช0.20x \ll 0.20):

4.0ร—10โˆ’4=4x2(0.80)(0.20)=4x20.164.0 \times 10^{-4} = \frac{4x^2}{(0.80)(0.20)} = \frac{4x^2}{0.16}

4x2=(4.0ร—10โˆ’4)(0.16)=6.4ร—10โˆ’54x^2 = (4.0 \times 10^{-4})(0.16) = 6.4 \times 10^{-5}

x2=1.6ร—10โˆ’5โ€…โ€ŠโŸนโ€…โ€Šx=4.0ร—10โˆ’3x^2 = 1.6 \times 10^{-5} \implies x = 4.0 \times 10^{-3}

5% Check: x0.20ร—100%=4.0ร—10โˆ’30.20ร—100%=2.0%\frac{x}{0.20} \times 100\% = \frac{4.0 \times 10^{-3}}{0.20} \times 100\% = 2.0\% โœ“ (< 5%)

Equilibrium:

  • [NO]=2(4.0ร—10โˆ’3)=8.0ร—10โˆ’3[\text{NO}] = 2(4.0 \times 10^{-3}) = 8.0 \times 10^{-3} M
  • [N2]โ‰ˆ0.80[\text{N}_2] \approx 0.80 M
  • [O2]โ‰ˆ0.20[\text{O}_2] \approx 0.20 M

The 5% Approximation ๐ŸŽฏ

Practice: Using the Approximation ๐Ÿงฎ

A(g)โ‡ŒB(g)+C(g)\text{A}(g) \rightleftharpoons \text{B}(g) + \text{C}(g), Kc=1.0ร—10โˆ’6K_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 0.50โˆ’xโ‰ˆ0.500.50 - x \approx 0.50:

1.0ร—10โˆ’6=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 ๐Ÿ”

Exit Quiz โ€” 5% Approximation โœ…

Part 5: ICE Tables with Kp

๐ŸงŠ When the Approximation Fails โ€” The Quadratic Formula

Part 5 of 7 โ€” Exact Solutions


Topics in This Part

Section
๐Ÿ“Œ The Quadratic Formula
In Equilibrium Problems
๐Ÿงช Worked Example

๐Ÿ”‘ Key Concept: Mastering this material will strengthen your foundation for both the AP Chemistry exam and more advanced chemistry topics.


What You'll Master in Part 5

  • Understanding the core concepts covered in Part 5
  • Applying these ideas to solve practice problems
  • Building toward AP exam readiness for this topic

๐Ÿ“Œ The Quadratic Formula

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

x=โˆ’bยฑb2โˆ’4ac2ax = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}


๐Ÿงช When to Use the Quadratic

TestConditionAction
Ratio check[initial]K<100\frac{[\text{initial}]}{K} < 100Must use quadratic
5% ruleApproximation yields > 5% changeMust use quadratic
KK relative to [C]0[C]_0KK is not very small vs. initial conc.Must use quadratic

โš ๏ธ Choosing the Correct Root

RootAccept?Why
Positive, gives [C]โ‰ฅ0[C] \geq 0โœ… YesPhysically meaningful
NegativeโŒ RejectConcentrations can't be negative
Larger than initial conc.โŒ RejectCan't lose more than you started with

โš ๏ธ Always check: Both roots of the quadratic, then reject the one that gives a negative or impossible concentration.

๐Ÿงช Worked Example

Problem: For A(g)โ‡ŒB(g)+C(g)\text{A}(g) \rightleftharpoons \text{B}(g) + \text{C}(g) with Kc=0.50K_c = 0.50, find the equilibrium concentrations given [A]=1.00[\text{A}] = 1.00 M, [B]=[C]=0[\text{B}] = [\text{C}] = 0.

Solution: Check approximation: 1.00/0.50=2.0<1001.00/0.50 = 2.0 < 100 โ†’ approximation NOT valid

ABC
I1.0000
Cโˆ’x-x+x+x+x+x
E1.00โˆ’x1.00-xxxxx

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

0.50(1.00โˆ’x)=x20.50(1.00 - x) = x^2

0.50โˆ’0.50x=x20.50 - 0.50x = x^2

x2+0.50xโˆ’0.50=0x^2 + 0.50x - 0.50 = 0

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

x=โˆ’0.50ยฑ(0.50)2โˆ’4(1)(โˆ’0.50)2(1)=โˆ’0.50ยฑ0.25+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=โˆ’0.50ยฑ2.252=โˆ’0.50ยฑ1.502x = \frac{-0.50 \pm \sqrt{2.25}}{2} = \frac{-0.50 \pm 1.50}{2}

Two roots:

  • x=โˆ’0.50+1.502=1.002=0.50x = \frac{-0.50 + 1.50}{2} = \frac{1.00}{2} = 0.50 โœ“
  • x=โˆ’0.50โˆ’1.502=โˆ’2.002=โˆ’1.00x = \frac{-0.50 - 1.50}{2} = \frac{-2.00}{2} = -1.00 โœ— (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 โœ“

๐Ÿ’ก Tip: 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\% โ†’ fails badly! Always verify with the 5% test.

Quadratic Approach ๐ŸŽฏ

Practice: Full Quadratic ๐Ÿงฎ

N2O4(g)โ‡Œ2โ€‰NO2(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+0.36xโˆ’0.18=04x^2 + 0.36x - 0.18 = 0

Using the quadratic formula:

1) What is the discriminant b2โˆ’4acb^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 ๐Ÿ”

Exit Quiz โ€” Quadratic Formula โœ…

Part 6: Problem-Solving Workshop

๐Ÿงฎ Problem-Solving Workshop: ICE Tables

Part 6 of 7 โ€” Multiple ICE Table Scenarios


Practice Makes Perfect

This workshop features multi-step problems that mirror the AP Chemistry exam format. Each problem requires you to combine concepts from previous parts and show your work clearly.

๐Ÿ”‘ Why this matters: The AP Chemistry exam rewards students who can apply concepts to unfamiliar problems โ€” structured practice is the best preparation.


What You'll Master in Part 6

  • Working through complete multi-step problems from start to finish
  • Building problem-solving strategies you can apply on the AP exam
  • Identifying which concepts to apply and in what order

๐Ÿ“Œ Decision Tree for ICE Table Problems

๐Ÿ”‘ Step 1 โ€” 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

๐Ÿ’ก Step 2 โ€” Can you use the approximation? Check: [initial]K>100\frac{[\text{initial}]}{K} > 100?

  • Yes โ†’ Approximate: [initial]โˆ’xโ‰ˆ[initial][\text{initial}] - x \approx [\text{initial}]
  • No โ†’ Full quadratic required

โš ๏ธ Step 3 โ€” 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(aโˆ’x)2\frac{(2x)^2}{(a-x)^2} โ†’ take square root
Small K with approxK=x2aK = \frac{x^2}{a} โ†’ x=Kax = \sqrt{Ka}
Full quadraticax2+bx+c=0ax^2 + bx + c = 0 โ†’ quadratic formula

Key Formulas

x=Kโ‹…[initial](small-Kย approximation)\boxed{x = \sqrt{K \cdot [\text{initial}]}} \quad \text{(small-K approximation)}

x=โˆ’bยฑb2โˆ’4ac2a(quadraticย formula)\boxed{x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a}} \quad \text{(quadratic formula)}

Problem 1: Finding K ๐Ÿงฎ

Problem: For 2โ€‰HI(g)โ‡ŒH2(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. Find KcK_c.

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 ๐Ÿงฎ

Problem: For COCl2(g)โ‡ŒCO(g)+Cl2(g)\text{COCl}_2(g) \rightleftharpoons \text{CO}(g) + \text{Cl}_2(g) with Kc=2.2ร—10โˆ’10K_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. Find the equilibrium concentrations.

Using the approximation 0.50โˆ’xโ‰ˆ0.500.50 - x \approx 0.50:

1) Solve: x=Kcร—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? ๐ŸŽฏ

Problem 4: Non-Zero Initial Products ๐Ÿงฎ

Problem: For H2(g)+I2(g)โ‡Œ2โ€‰HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\,\text{HI}(g) with 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. Find the equilibrium concentrations.

Solution: 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+2x0.50โˆ’x8 = \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 โ€” ICE Table Workshop โœ…

Part 7: Synthesis & AP Review

๐ŸŽ“ Synthesis & AP Review

Part 7 of 7 โ€” ICE Tables and Equilibrium Calculations


Bringing It All Together

This comprehensive review connects every concept from Parts 1โ€“6 with AP-style problems. The questions are designed to mirror what you'll see on the actual exam โ€” multi-step, multi-concept, and requiring clear written explanations.

๐Ÿ”‘ Why this matters: AP Chemistry exam questions rarely test one concept in isolation โ€” success requires connecting ideas across topics.


What You'll Master in Part 7

  • Solving AP-style questions that integrate multiple concepts from this unit
  • Writing clear, concise explanations using proper chemistry terminology
  • Identifying and avoiding common AP exam traps and mistakes

๐Ÿ“‹ Complete ICE Table Summary

The ICE Table

ReactantProduct
IInitial concentrationInitial concentration (often 0)
Cโˆ’(-(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 โ†’ 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

Key Formulas

E=I+C(forย eachย species)\boxed{E = I + C \quad \text{(for each species)}}

x[initial]ร—100%<5%(validationย test)\boxed{\frac{x}{[\text{initial}]} \times 100\% < 5\% \quad \text{(validation test)}}


๐Ÿ”‘ Verification: Always check โ€” plug equilibrium concentrations back into the K expression. The calculated K should match the given K.


๐Ÿ’ก Tip: For a quick mental check, confirm all equilibrium concentrations are non-negative and that the shift direction is consistent with QQ vs KK.


โš ๏ธ Warning: The most common ICE table error is forgetting that stoichiometric coefficients multiply xx in the Change row โ€” e.g., for 2Aโ‡ŒB2\text{A} \rightleftharpoons \text{B}, ฮ”[A]=โˆ’2x\Delta[\text{A}] = -2x, not โˆ’x-x.

AP-Style Multiple Choice โ€” Set 1 ๐ŸŽฏ

AP Free-Response Style ๐Ÿงฎ

Problem: For CO(g)+Cl2(g)โ‡ŒCOCl2(g)\text{CO}(g) + \text{Cl}_2(g) \rightleftharpoons \text{COCl}_2(g) with Kc=255K_c = 255 at 100ยฐC, a 1.00 L flask is charged with 0.400 mol CO and 0.400 mol Cl2Cl_{2}. No COCl2COCl_{2} 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(0.400โˆ’x)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 COCl2COCl_{2} formed? (Enter in mol)

Round all answers to 3 significant figures.

Final Concept Review ๐Ÿ”

Final Exit Quiz โœ