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๐ŸงชAP Chemistry Unit 7 Review

7.3 Reaction Quotient and Equilibrium Constant

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  3. Unit 7 โ€“ Equilibrium
  4. Topic: 7.3
๐ŸงชAP Chemistry
Unit 7 Review

7.3 Reaction Quotient and Equilibrium Constant

Written by the Fiveable Content Team โ€ข Last updated August 2025
Verified for the 2026 exam
Verified for the 2026 examโ€ขWritten by the Fiveable Content Team โ€ข Last updated August 2025
๐ŸงชAP Chemistry
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Unit 5 Overview: Kinetics
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6.1 Endothermic and Exothermic Processes
6.2 Energy Diagrams
6.3 Heat Transfer and Thermal Equilibrium
6.4 Heat Capacity and Calorimetry
6.5 Energy of Phase Changes
6.6 Introduction to Enthalpy of Reaction
6.7 Bond Enthalpies
6.8 Enthalpy of Formation
6.9 Hessโ€™s Law

Unit 7 โ€“ Equilibrium

Unit 7 Overview: Equilibrium
7.1 Introduction to Equilibrium
7.2 Direction of Reversible Reactions
7.3 Reaction Quotient and Equilibrium Constant
7.4 Calculating the Equilibrium Constant
7.5 Magnitude of the Equilibrium Constant
7.6 Properties of the Equilibrium Constant
7.7 Calculating Equilibrium Concentrations
7.8 Representations of Equilibrium
7.9 Introduction to Le Chรขtelierโ€™s Principle
7.10 Reaction Quotient and Le Chรขtelierโ€™s Principle
8.11 pH and Solubility
7.11 Introduction to Solubility Equilibria
7.12 Common Ion Effect
7.14 Free Energy of Dissolution

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8.1 Introduction to Acids and Bases
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8.3 Weak Acid and Base Equilibria
8.4 Acid-Base Reactions and Buffers
8.5 Acid-Base Titrations
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Unit 9 Review: Thermodynamics and Electrochemistry
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9.4 Thermodynamic and Kinetic Control
9.5 Free Energy and Equilibrium
9.6 Free Energy of Dissolution
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Separation of Solutions and Mixture Chromatography
Spectroscopy and Electromagnetic Spectrum
Photoelectric Effect
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So far, weโ€™ve talked exclusively about reactions at equilibrium. However, reactions can be at any point! They can be pre-equilibrium, post-equilibrium, or at equilibrium. We can describe where a reaction is in the process of reaching equilibrium by calculating Q, the reaction quotient.

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Practice Questions for 7.3

1 of 10

A student determines the number of moles of HIHIHI, H2H_2H2โ€‹, and I2I_2I2โ€‹ in a reaction vessel at a specific time. To calculate QcQ_cQcโ€‹ for 2HI(g)โ‡ŒH2(g)+I2(g)2HI(g) \rightleftharpoons H_2(g) + I_2(g)2HI(g)โ‡ŒH2โ€‹(g)+I2โ€‹(g), which additional quantity is required?

A.

The temperature of the gases

B.

The equilibrium constant KcK_cKcโ€‹

C.

The total pressure of gases

D.

The volume of the container

Vocabulary

The following words are mentioned explicitly in the College Board Course and Exam Description for this topic.

Term

Definition

equilibrium constant

A numerical value that expresses the ratio of products to reactants at equilibrium, indicating the extent to which a reaction proceeds.

equilibrium expression

A mathematical equation that relates the concentrations or partial pressures of reactants and products at equilibrium, expressed as Kc or Kp.

Kc

The equilibrium constant expressed in terms of molar concentrations of reactants and products at equilibrium.

Kp

The equilibrium constant expressed in terms of partial pressures of gaseous reactants and products at equilibrium.

law of mass action

The principle that the equilibrium expression for a reversible reaction is the ratio of the concentrations (or partial pressures) of products to reactants, each raised to the power of their stoichiometric coefficients.

partial pressure

The pressure exerted by a single gas in a mixture of gases, used in equilibrium expressions for gas-phase reactions.

reaction quotient

A value calculated using the same expression as the equilibrium constant but using current (non-equilibrium) concentrations or partial pressures.

reversible reaction

A chemical reaction that can proceed in both the forward and reverse directions, with reactants forming products and products reforming reactants.

Frequently Asked Questions

What is the reaction quotient Q and how is it different from the equilibrium constant K?

Q is the reaction quotientโ€”the same algebraic form as the equilibrium constant but using concentrations (or partial pressures) at any moment: for aA + bB โ‡Œ cC + dD, Qc = [C]^c[D]^d / [A]^a[B]^b (and Qp uses partial pressures). K is the value of that ratio specifically at equilibrium (Kc or Kp). Key differences for AP Chem: (1) Q tells you where the reaction currently is; K tells you where it will be at equilibrium. If Q < K the reaction shifts toward products; if Q > K it shifts toward reactants; if Q = K the system is at equilibrium. (2) Neither Q nor K includes pure solids or liquids (their activities are constant). Remember the exam wonโ€™t test converting Kcโ†”Kpโ€”just know conceptual differences. For a focused review check Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat), the unit overview (https://library.fiveable.me/ap-chemistry/unit-7), and practice problems (https://library.fiveable.me/practice/ap-chemistry).

Why do we use brackets for concentrations but parentheses for partial pressures in equilibrium expressions?

Brackets [ ] are the shorthand chemists use for molar concentration (molยทLโปยน), so Kc and Qc are built from [A], [B], etc. Parentheses ( ) around a symbol mean the partial pressure of a gas (usually in atm), so Kp and Qp use (PA), (PB), etc. Practically itโ€™s just a notation convention that tells you which physical measure youโ€™re using in the law of mass action: concentrations for Kc/Qc, partial pressures for Kp/Qp. Behind that is the idea of โ€œactivityโ€โ€”for ideal gases activity โ‰ˆ partial pressure, for solutes activity โ‰ˆ concentrationโ€”but on the AP exam you only need to recognize and use Kc vs Kp and omit pure solids/liquids from expressions (CED Topic 7.3). For more review, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and the unit overview (https://library.fiveable.me/ap-chemistry/unit-7). For extra practice, check the AP Chem practice problems (https://library.fiveable.me/practice/ap-chemistry).

How do I write the equilibrium expression for a chemical equation?

Write the equilibrium expression from the balanced equation using the law of mass action. For a general reaction a A + b B โ‡Œ c C + d D - Kc (or Qc at any moment) = [C]^c [D]^d / ([A]^a [B]^bโ€”concentrations in molยทLโปยน). - For gases use Kp (or Qp) with partial pressures: Kp = (P_C)^c (P_D)^d / (P_A)^a (P_B)^b. - Use the stoichiometric coefficients as exponents. - Omit pure solids and pure liquids from Q or K because their concentrations (activities) are essentially constant (e.g., CaCO3(s) or H2O(l) are left out). To write one quickly: balance the equation, put products over reactants, raise each concentration/pressure to its coefficient, and decide Kc vs Kp based on whether youโ€™re given concentrations or partial pressures. Remember Q has the same form as K; compare Q to K to predict the reactionโ€™s shift. For a refresher and examples see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat), the Unit 7 overview (https://library.fiveable.me/ap-chemistry/unit-7), and extra practice problems (https://library.fiveable.me/practice/ap-chemistry).

I'm confused about when to use Kc versus Kp - can someone explain the difference?

Use Kc when you write the equilibrium expression with concentrations [ ] (molarity); use Kp when you write it with partial pressures P (for gases). For a general reaction aA + bB โ‡Œ cC + dD: - Kc = [C]^c[D]^d / [A]^a[B]^b (Qc is the same form at any time) - Kp = (PC)^c(PD)^d / (PA)^a(PB)^b (Qp is the reaction quotient in pressures) If species are pure solids or pure liquids, you leave them out of K expressions because their concentrations/activities donโ€™t change. At equilibrium Q โ†’ K, so at equilibrium Qc = Kc and Qp = Kp. On the AP exam, pay attention to which form the question gives (concentrations vs. partial pressures). The CED says you donโ€™t need to convert Kc โ‡„ Kp for the exam, but you should understand the conceptual difference (Topic 7.3). For a quick refresher, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and the unit overview (https://library.fiveable.me/ap-chemistry/unit-7). For more practice problems, check (https://library.fiveable.me/practice/ap-chemistry).

What's the law of mass action and why do we need to know it?

The law of mass action says that for a reaction a A + b B โ‡Œ c C + d D, the equilibrium state is described by a constant K whose expression is [C]^c[D]^d / [A]^a[B]^b (or with partial pressures for Kp). Itโ€™s important because K (and the reaction quotient Q, the same expression at any time) tells you the equilibrium position: if Q < K the reaction goes forward, if Q > K it goes reverse, and at equilibrium Q = K. Practically, you use it to predict direction of shift, set up ICE tables, and solve equilibrium concentrationsโ€”key AP skills in Topic 7.3 and 7.4. Remember pure solids and liquids donโ€™t appear in K or Q. For more review and worked examples see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat), the Unit 7 overview (https://library.fiveable.me/ap-chemistry/unit-7), and practice questions (https://library.fiveable.me/practice/ap-chemistry).

Why don't we include solids and liquids in equilibrium expressions?

Short answer: solids and pure liquids arenโ€™t in K or Q because their concentrations (more correctly, their activities) donโ€™t change during the reaction. For a pure solid or pure liquid, the โ€œconcentrationโ€ depends only on density and molar mass, not on how much of that phase you have, so itโ€™s effectively constant. The law of mass action (K = [products]^c/[reactants]^aโ€ฆ) therefore omits species whose amounts donโ€™t affect the equilibrium positionโ€”these are heterogeneous equilibria. This is exactly what the CED states in 7.3.A.2: donโ€™t include substances whose concentrations or partial pressures are independent of the amount, such as solids and pure liquids. (If you need the formal treatment, chemists use activities to be precise; for AP you can just say โ€œconstant so omitted.โ€) For more practice and examples, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) or the Unit 7 overview (https://library.fiveable.me/ap-chemistry/unit-7).

How do you calculate Q if you're given concentrations at a random time during the reaction?

Write the reactionโ€™s Q expression from the balanced equation (use concentrations for Qc or partial pressures for Qp). For aA + bB โ‡Œ cC + dD: Qc = [C]^c[D]^d / [A]^a[B]^b Then plug in the concentrations at that time (raise each to its stoichiometric exponent) and ignore pure solids or liquids (they donโ€™t appear in Q). Example: if at some time [A] = 0.20 M, [B] = 0.10 M, [C] = 0.50 M for A + 2B โ‡Œ C, then Qc = [C] / ([A][B]^2) = 0.50 / (0.20 ร— 0.10^2) = 0.50 / (0.20 ร— 0.01) = 0.50 / 0.002 = 250. Compare Q to K: Q < K (shifts right), Q = K (at equilibrium), Q > K (shifts left). For more practice and the AP-aligned summary, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and lots of practice problems (https://library.fiveable.me/practice/ap-chemistry).

What does it mean when Q equals K at equilibrium?

If Q = K, the system is at equilibriumโ€”meaning the relative concentrations (or partial pressures) of reactants and products match the equilibrium constant, so thereโ€™s no net change in composition over time. Microscopically itโ€™s dynamic: forward and reverse reaction rates are equal, so molecules keep reacting but the macroscopic amounts stay constant. Use Qc/Kc for concentrations and Qp/Kp for gases; pure solids and liquids arenโ€™t included in the Q expression. If Q โ‰  K, the reaction will shift (via more forward or reverse reaction) until Q moves to equal K (ICE tables are a common way to show that mathematically). Note: on the AP exam you wonโ€™t be asked to convert Kc โ†” Kp, but you should be comfortable writing Q and K expressions and predicting shift directions (Topic 7.3 study guide: https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat; unit overview: https://library.fiveable.me/ap-chemistry/unit-7). For extra practice, try problems at https://library.fiveable.me/practice/ap-chemistry.

I don't understand why the exponents in the equilibrium expression match the coefficients in the balanced equation - why is that?

Good questionโ€”the exponents equal the coefficients because of the law of mass action and how equilibrium is defined. Two linked ways to think about it: - Kinetics view (easy intuition): for an elementary step, the rate of the forward reaction depends on how often the reactant particles collide. If the balanced elementary reaction is aA + bB โ†’ ..., the collision frequencyโ€”and so the rateโ€”is proportional to [A]^a[B]^b. At equilibrium the forward and reverse rates balance, so the concentrations enter the equilibrium expression with those powers. - Thermodynamics view (more general): equilibrium comes from equal chemical potentials. When you express that equality using activities (or concentrations for AP work), the math yields a product of activities raised to the stoichiometric coefficients. Thatโ€™s why Kc = [C]^c[D]^d / [A]^a[B]^b. Pure solids and liquids drop out because their activity is ~1 (so they donโ€™t appear). This is exactly what the CED calls the law of mass action for Kc/Qc (Topic 7.3). If you want a quick refresher or practice, check the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and try some practice problems at (https://library.fiveable.me/practice/ap-chemistry).

Can someone explain step by step how to set up an equilibrium expression from a chemical equation?

Start with the balanced chemical equation. Then follow these steps: 1. Identify phases: include only gases and aqueous species in the expression; exclude pure solids and pure liquids (CED 7.3.A.2). 2. Write product concentrations (or partial pressures) in the numerator and reactant ones in the denominator. 3. Use stoichiometric coefficients as exponents. For aA + bB โ‡Œ cC + dD: Kc = [C]^c[D]^d / [A]^a[B]^b (or Kp using partial pressures: Kp = (PC)^c(PD)^d/(PA)^a(PB)^b). 4. For a snapshot at any time use Q (Qc or Qp) with the same form; at equilibrium Q = K. Compare Q and K to predict shift (Q < K โ†’ shift right; Q > K โ†’ shift left). Quick AP notes: show the balanced equation, use correct phases, and label whether youโ€™re using Kc or Kp (AP wonโ€™t test conversions between them). For a targeted review, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and more practice problems (https://library.fiveable.me/practice/ap-chemistry).

What happens to the equilibrium expression if I reverse the chemical equation?

If you reverse a chemical equation, the equilibrium expression becomes the reciprocal. For example, if for aA + bB โ‡Œ cC + dD you have K = [C]^c[D]^d / [A]^a[B]^b, then for the reversed reaction (cC + dD โ‡Œ aA + bB) Krev = 1/K = [A]^a[B]^b / [C]^c[D]^d. More generally, if you multiply the entire balanced equation by a factor n, the new K equals the original K raised to the n power (Knew = K^n). Remember to keep Kc vs Kp consistent (use concentrations for Kc, partial pressures for Kp) and omit pure solids and liquids from the expression because their activities are constant (CED Topic 7.3). For a quick refresher, see the Topic 7.3 study guide on Fiveable (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat), and practice problems at (https://library.fiveable.me/practice/ap-chemistry).

Why do pure liquids and solids not appear in Kc or Kp expressions?

Because Kc and Kp (or Q) come from the law of mass action, they use the concentrations (or partial pressures) of species that change as the reaction shifts. Pure solids and pure liquids have fixed densities and therefore constant concentrations (or activities) at a given temperatureโ€”their โ€œeffective concentrationโ€ doesnโ€™t change when you add or remove some of that phase unless you remove it entirely. So including them would just multiply K by a constant; AP practice omits them and either treats their activity as 1 or absorbs that constant into K. Thatโ€™s why heterogeneous equilibrium expressions only list gases and aqueous species (CED 7.3.A.2). If you want a deeper look or examples (ICE tables, activities), check the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) or the Unit 7 overview (https://library.fiveable.me/ap-chemistry/unit-7). For extra practice, use Fiveableโ€™s AP Chem problems (https://library.fiveable.me/practice/ap-chemistry).

How do I know whether a problem is asking for Kc or Kp?

Look at what the problem gives or asks for: if it uses concentrations (mol/L or [X]) you need Kc (or Qc); if it uses partial pressures (atm or PX) you need Kp (or Qp). For gas-phase reactions you can write either form, but the AP exam will tell you which one by the units it uses. Remember pure solids and pure liquids donโ€™t appear in the equilibrium expression (theyโ€™re omitted from Kc or Kp). Also watch wording: โ€œpartial pressureโ€ or โ€œatmโ€ โ†’ Kp; โ€œ[ ]โ€, โ€œmolarityโ€, or โ€œMโ€ โ†’ Kc. Donโ€™t try to convert Kcโ†”Kp on the exam (that conversion wonโ€™t be tested). If youโ€™re unsure, scan for what the reaction mixture is described inโ€”concentrations or pressuresโ€”and use that form. For more practice and examples see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and Unit 7 resources (https://library.fiveable.me/ap-chemistry/unit-7). For extra practice try the AP problems set (https://library.fiveable.me/practice/ap-chemistry).

What's the difference between the reaction quotient at any time versus at equilibrium?

The reaction quotient Q (or Qc/Qp) is the same formula as the equilibrium expression but evaluated at any momentโ€”it uses the current concentrations (or partial pressures) of reactants and products. K (Kc or Kp) is that expression evaluated at equilibrium and is constant for a given reaction at a fixed temperature. Key points you need for AP Chem: - If Q < K, the net reaction shifts right (forms more products). If Q > K, it shifts left (forms more reactants). If Q = K, the system is at dynamic equilibrium. - Q is time-dependent; K is time-independent (at constant T). - Donโ€™t include pure solids or pure liquids in Q or K expressions (theyโ€™re omitted). - For gases use Qp/Kp; for solutions use Qc/Kc. For a clear walkthrough and examples, see the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat). More unit review (https://library.fiveable.me/ap-chemistry/unit-7) and practice Qs (https://library.fiveable.me/practice/ap-chemistry) are great for drilling this.

I'm studying for the AP exam - do I need to memorize how to convert between Kc and Kp?

Short answer: Noโ€”you donโ€™t have to memorize converting Kc โ†” Kp for the AP exam. The CED explicitly excludes conversion between Kc and Kp from assessment, so you wonโ€™t be asked to do those conversions on the test. That said, you should understand the conceptual difference: Kc uses concentrations, Kp uses partial pressures, and for gas-phase reactions they both express the same equilibrium idea (Kc = Qc, Kp = Qp). Itโ€™s helpful to know qualitatively that Kp and Kc can differ when the number of moles of gas changes (ฮ”n โ‰  0), and to pay attention to which form a question gives you. If you want a quick refresher or practice on these ideas (not conversion problems), check the Topic 7.3 study guide (https://library.fiveable.me/ap-chemistry/unit-7/reaction-quotient-equilibrium-constant/study-guide/Y12LZEr3OWIAqV3gErat) and the Unit 7 overview (https://library.fiveable.me/ap-chemistry/unit-7). For lots of practice problems, see (https://library.fiveable.me/practice/ap-chemistry).

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math & computer science

๐Ÿงฎ ap calculus abโ™พ๏ธ ap calculus bc๐Ÿ“ ap precalculus๐Ÿ“Š ap statistics๐Ÿ’ป ap computer science aโŒจ๏ธ ap computer science p

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7.10 Reaction Quotient and Le Chรขtelierโ€™s Principle

In the last section, we discussed the concept of Le Chรขtelierโ€™s Principle and described how it can be used to predict changes in concentrations as a result of external stress being placed upon a system. However, why does Le Chรขtelierโ€™s Principle actually work? We learned some rules last time and sort of โ€œlogic'dโ€ it out, but in this guide, weโ€™ll take a look at how Le Chรขtelierโ€™s Principle is justified by using Q, the reaction quotient.

Review of the Reaction Quotient, Q

Earlier in this unit, we discussed the value Q, a number called the reaction quotient. We examined how this value could tell us how an equilibrium would shift based on conditions not at equilibrium. For example, if we found that Q was less than the assigned K value for a reaction, our reaction would respond by increasing the concentration of products in order for Q to become K. Remember that when Q = K, our system is at equilibrium and thus there will be no more changes in concentrations all else held equal. A reaction will basically proceed to make Q equal to K.

The formulas for Q and K look exactly the same, but remember that with Q we can calculate the value at any concentration, whereas at K it is only equilibrium concentrations. This way of thinking about Q vs. K will help guide our mathematical justification of Le Chรขtelierโ€™s Principle for concentration and pressure, but weโ€™ll also see how temperature stands out as an exception to using Q to justify.

Applying Q To Le Chรขtelierโ€™s Principle

Concentration

As we learned in the last section, increasing the concentration of products or reactants will cause the system to respond by creating more of the other side. For example in reaction A โ‡Œ B if the concentration of B was increased, the system would respond by increasing the production of A and vice versa. Letโ€™s think about how Q might help us understand why this occurs.