Topic 7.6: Properties of the Equilibrium Constant Quiz

Master AP Chemistry Topic 7.6 with this free practice quiz. Test your skills on inverting k, raising k to a power, and multiplying k values for added steps to prepare for your AP exam.

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Topic 7.6: Properties of the Equilibrium Constant Quiz

18 MCQs

Master the properties of the equilibrium constant with these 18 MCQs on AP Chemistry Topic 7.6: Properties of the Equilibrium Constant.

Covered Subtopics: Manipulating K when equations change, adding reactions, combining equilibrium constants

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1. For A(g) ⇌ B(g), K = 3.0. What is the equilibrium constant for 2A(g) ⇌ 2B(g)?

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2. Consider the steps: (1) A(g) ⇌ B(g), K₁ = 0.50; (2) B(g) ⇌ C(g), K₂ = 4.0. What is K for the overall reaction A(g) ⇌ C(g)?

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3. For a reaction with K = 36, what is K for the same reaction written in reverse with all coefficients halved?

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4. Consider the steps: (1) A(g) ⇌ B(g), K₁ = 2.0; (2) 2B(g) ⇌ C(g), K₂ = 9.0. What is K for the overall reaction 2A(g) ⇌ C(g)?

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5. The forward reaction A(g) ⇌ B(g) has K = 0.25. Which statement about the reverse reaction B(g) ⇌ A(g) is correct?

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6. For A(g) + B(g) ⇌ C(g), K = 12. What is K for 2C(g) ⇌ 2A(g) + 2B(g)?

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7. Consider the steps: (1) 2A(g) ⇌ B(g) + C(g), K₁ = 4.0; (2) B(g) ⇌ 2D(g), K₂ = 0.50. What is K for the overall reaction 2A(g) ⇌ C(g) + 2D(g)?

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8. A student multiplies a reaction equation by 3 and claims the new equilibrium constant is three times the original. What is the error?

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9. Consider the steps: (1) P(g) ⇌ Q(g) + R(g), K₁ = 3.0; (2) Q(g) ⇌ S(g), K₂ = 2.0. What is K for the overall reaction P(g) ⇌ R(g) + S(g)?

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10. Consider the two steps: (1) A(g) ⇌ B(g), K₁ = 2.0; (2) B(g) ⇌ C(g), K₂ = 5.0. What is K for the overall reaction A(g) ⇌ C(g)?

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11. For 1/2 N₂(g) + 1/2 O₂(g) ⇌ NO(g), K = 2.1 x 10⁻¹⁶. What is K for N₂(g) + O₂(g) ⇌ 2NO(g)?

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12. Given K₁ = 5.0 for A(g) ⇌ B(g) and K₂ = 0.10 for C(g) ⇌ B(g), what is K for A(g) ⇌ C(g)?

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13. For N₂(g) + 3H₂(g) ⇌ 2NH₃(g), K = 6.0 x 10⁵. What is K for 2NH₃(g) ⇌ N₂(g) + 3H₂(g)?

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14. Two reactions are added together to obtain an overall reaction. How is the overall equilibrium constant related to the constants of the two steps?

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15. For 2SO₂(g) + O₂(g) ⇌ 2SO₃(g), K = 2.5 x 10². What is K for SO₂(g) + 1/2 O₂(g) ⇌ SO₃(g)?

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16. If every coefficient in a balanced equation is doubled, what happens to the equilibrium constant?

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17. Consider the steps: (1) X(g) ⇌ Y(g), K₁ = 10; (2) Y(g) ⇌ Z(g), K₂ = 0.20. What is K for the overall reaction X(g) ⇌ Z(g)?

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18. For A(g) ⇌ B(g), K = 4.0. What is the equilibrium constant for the reverse reaction, B(g) ⇌ A(g)?

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K Belongs to the Equation as Written

Every equilibrium constant is tied to one exact way of writing the reaction, at one stated temperature. Change the writing and the constant changes, even though the chemistry in the flask is untouched.

Each rule follows directly from the shape of the K expression: products over reactants, every concentration raised to its coefficient.

Reversing the Equation Inverts K

Reversing a reaction swaps the numerator and denominator of its expression. Products become reactants and reactants become products, so the new constant is the reciprocal of the old one:

K reverse = 1 / K forward

For N₂(g) + 3H₂(g) ⇌ 2NH₃(g), K = 6.0 × 10⁵ at the stated temperature. Written in reverse, 2NH₃(g) ⇌ N₂(g) + 3H₂(g) has K = 1 / (6.0 × 10⁵) = 1.7 × 10⁻⁶.

A forward reaction that strongly favours products has a reverse reaction that favours reactants by the same measure, because it is the same mixture read from the other side.

Multiplying the Coefficients Raises K to a Power

Multiplying every coefficient by a number n raises every concentration in the expression to n times its former power. The whole expression is therefore raised to the power n: the new constant is Kⁿ.

Doubling A(g) ⇌ B(g) with K = 3.0 gives 2A(g) ⇌ 2B(g) with K = 3.0² = 9.0. Tripling gives K³. The constant is never multiplied by n itself: scaling the equation and scaling the constant are different operations. For ½N₂(g) + ½O₂(g) ⇌ NO(g), K = 2.1 × 10⁻¹⁶, doubling gives K = (2.1 × 10⁻¹⁶)² = 4.4 × 10⁻³² for N₂(g) + O₂(g) ⇌ 2NO(g).

Dividing the Coefficients Takes the Root

Dividing is the same rule with a fraction for n. Halving every coefficient raises K to the one half power, which is taking the square root.

For 2SO₂(g) + O₂(g) ⇌ 2SO₃(g), K = 2.5 × 10². The halved equation, SO₂(g) + ½O₂(g) ⇌ SO₃(g), has K = √(2.5 × 10²) = 15.8, about 16.

An equation written per mole of one chosen species is often the most useful form, and its K is simply the corresponding root of the original.

Adding Reactions Multiplies Their K Values

When two reactions are added and a species appearing on both sides cancels, that species is an intermediate, and the overall constant is the product of the step constants:

K overall = K₁ × K₂

Multiplying the two step expressions puts the intermediate once in a numerator and once in a denominator, so it cancels, leaving exactly the expression of the overall reaction.

Steps can be prepared before adding. A step used twice enters with its K squared; a step used in reverse enters with its reciprocal. Each manipulation is applied to the step’s K in the same way it is applied to the step’s equation, and only then are the prepared constants multiplied. Doubling a step squares its K before adding: A(g) ⇌ B(g) with K₁ = 2.0 doubled gives 4.0, and with 2B(g) ⇌ C(g), K₂ = 9.0, the overall K is 36. Reversing a step inverts its K first: K₁ = 5.0 with K₂ = 0.10 reversed to 10 gives an overall K of 50 for A(g) ⇌ C(g).

Combining Manipulations in the Right Order

Many questions apply two manipulations to one reaction: reverse it and halve it, or double one step and then add it to another. The safe method is to transform the constant step by step, in the same order the equation is transformed, writing the new K after each single change.

Order between reversing and scaling does not alter the final result, because a reciprocal and a power commute. What matters is that every manipulation applied to the equation is applied once, and only once, to the constant. For A(g) + B(g) ⇌ C(g), K = 12, the reversed and doubled 2C(g) ⇌ 2A(g) + 2B(g) has K = (1 / 12)² = 6.9 × 10⁻³.

Only Temperature Gives a Different K for the Same Equation

For one fixed way of writing the equation, K is set by temperature alone. Changing concentrations, changing the pressure or volume, or adding a catalyst changes the mixture or the timing, and the mixture then satisfies the same K as before.

Rewriting the equation produces a different constant for the same mixture, while changing the temperature produces a different constant because the mixture settles somewhere new.

Worked Examples

Example 1: reversing, checked against a real mixture. For H₂(g) + I₂(g) ⇌ 2HI(g), Kc = 54, and Topic 7.5 used the equilibrium row [H₂] = [I₂] = 0.214 and [HI] = 1.57 mol L⁻¹. The reverse reaction, 2HI(g) ⇌ H₂(g) + I₂(g), has K = 1 / 54 = 0.019. Check with the same mixture: (0.214 × 0.214) / (1.57)² = 0.019. One mixture, two constants, each correct for its own direction.

Example 2: halving, checked against a real mixture. For 2SO₂(g) + O₂(g) ⇌ 2SO₃(g), the mixture [SO₂] = 0.20, [O₂] = 0.10 and [SO₃] = 1.0 mol L⁻¹ gives K = (1.0)² / ((0.20)² × 0.10) = 2.5 × 10². The halved equation SO₂(g) + ½O₂(g) ⇌ SO₃(g) applied to the same mixture gives 1.0 / (0.20 × √(0.10)) = 15.8, which is √(2.5 × 10²), as the rule requires.

Example 3: adding two steps. Step 1: A(g) ⇌ B(g), K₁ = 2.0. Step 2: B(g) ⇌ C(g), K₂ = 5.0. Adding cancels B, giving A(g) ⇌ C(g) with K = 2.0 × 5.0 = 10. A single mixture confirms it: [A] = 0.30, [B] = 0.60 and [C] = 3.0 mol L⁻¹ gives 0.60 / 0.30 = 2.0 for step 1, 3.0 / 0.60 = 5.0 for step 2, and 3.0 / 0.30 = 10 for the overall reaction.

Example 4: two manipulations combined. For 2A(g) ⇌ B(g), K = 36; the mixture [A] = 0.10 and [B] = 0.36 mol L⁻¹ confirms it, since 0.36 / (0.10)² = 36. Write the reaction in reverse with all coefficients halved: ½B(g) ⇌ A(g). Reverse first: K becomes 1 / 36. Then halve: take the square root. K = √(1 / 36) = 1 / 6 = 0.17. The same mixture agrees: 0.10 / √(0.36) = 0.10 / 0.60 = 0.17.

Traps That Cost Marks in Topic 7.6

“Doubling the equation doubles K.” Doubling raises K to the second power. K = 3.0 becomes 9.0, not 6.0.

“The reverse reaction has K equal to negative K.” K is a ratio of concentrations and is never negative. Reversing gives the reciprocal: K = 0.25 forward means K = 4.0 in reverse.

“Adding two reactions adds their constants.” Adding reactions multiplies the constants, because the expressions themselves multiply and the intermediate cancels. Steps with K₁ = 2.0 and K₂ = 5.0 combine to 10, never to 7.0.

“Halving the equation halves K.” Halving takes the square root. K = 2.5 × 10² becomes about 16, not 1.25 × 10².

“The manipulated K can be used with the original equation.” Each constant belongs to its own written form. Using √(K) in a calculation set up with the doubled equation mixes two different constants and gives a wrong answer, even though both values describe the same flask.

“A bigger K after rewriting means the reaction now favours products more.” Rewriting changes nothing in the flask. K = 36 for 2A(g) ⇌ B(g) and K = 6.0 for A(g) ⇌ ½B(g) describe the identical equilibrium mixture.

Key Relationships

  • Reversing a reaction gives the reciprocal constant: K reverse = 1 / K forward
  • Multiplying every coefficient by n raises the constant to the power n: K new = (K old)ⁿ
  • Halving every coefficient takes the square root: K new = √(K old)
  • Adding reactions multiplies their constants, and any species that cancels is an intermediate
  • A step must be prepared before adding: reversed steps contribute their reciprocal, and steps used n times contribute Kⁿ
  • Combined manipulations apply in sequence: reverse then halve K = 36 gives √(1 / 36) = 0.17
  • K is never negative, and a manipulated K is valid only for the equation in its manipulated form
  • For a fixed written equation, only temperature changes K; concentration, pressure, volume and catalysts do not

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