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AP Chemistry connects many chemistry topics into a few major ideas about matter, energy, structure, and change. This cheat sheet summarizes the relationships students use most often when solving AP-style problems. It is designed to help students review formulas, recognize patterns, and choose the right model quickly.

The focus is on core principles rather than isolated facts.

The most important ideas include how particles determine properties, how energy changes drive or resist reactions, and how systems reach equilibrium. Students should be fluent with mole relationships, gas laws, equilibrium expressions, acid-base calculations, thermodynamics, kinetics, and electrochemical equations. Many AP questions require connecting particle-level explanations to equations and data.

Strong answers usually combine a correct formula, correct units, and a clear explanation of cause and effect.

Key Facts

  • The mole relationship is n=mMn = \frac{m}{M}, where nn is moles, mm is mass, and MM is molar mass.
  • For ideal gases, PV=nRTPV = nRT, where PP is pressure, VV is volume, nn is moles, RR is the gas constant, and TT is temperature in kelvins.
  • An equilibrium constant is written as K=[products]coefficients[reactants]coefficientsK = \frac{[\text{products}]^{\text{coefficients}}}{[\text{reactants}]^{\text{coefficients}}}, omitting pure solids and pure liquids.
  • For acids and bases, pH=log[H+]\mathrm{pH} = -\log[\mathrm{H^+}] and pOH=log[OH]\mathrm{pOH} = -\log[\mathrm{OH^-}], with pH+pOH=14.00\mathrm{pH} + \mathrm{pOH} = 14.00 at 25C25^\circ\mathrm{C}.
  • The Gibbs free energy relationship is ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S, and a process is thermodynamically favorable when ΔG<0\Delta G < 0.
  • The rate law has the form rate=k[A]m[B]n\text{rate} = k[A]^m[B]^n, and the exponents must be determined experimentally rather than from the balanced equation.
  • Electrochemical cell potential is related to free energy by ΔG=nFEcell\Delta G^\circ = -nFE^\circ_{\text{cell}}, so a positive EcellE^\circ_{\text{cell}} gives a negative ΔG\Delta G^\circ.
  • The Nernst equation is E=E0.0592nlogQE = E^\circ - \frac{0.0592}{n}\log Q at 25C25^\circ\mathrm{C}, showing how concentration affects cell voltage.

Vocabulary

Equilibrium
A dynamic state in which the forward and reverse reaction rates are equal and concentrations remain constant.
Enthalpy
The heat energy change of a system at constant pressure, represented by ΔH\Delta H.
Entropy
A measure of energy dispersal or particle arrangement disorder, represented by ΔS\Delta S.
Activation Energy
The minimum energy particles must have to react successfully, represented by EaE_a.
Oxidation
The loss of electrons by a substance, which increases its oxidation number.
Buffer
A solution containing a weak acid and its conjugate base, or a weak base and its conjugate acid, that resists changes in pH\mathrm{pH}.

Common Mistakes to Avoid

  • Using Celsius in gas law or thermodynamics equations is wrong because formulas such as PV=nRTPV = nRT and ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S require temperature in kelvins.
  • Including solids or liquids in KK expressions is wrong because pure solids and pure liquids have constant activity and are omitted from equilibrium expressions.
  • Reading rate law exponents from the balanced equation is wrong for most mechanisms because rate orders must come from experimental data unless the step is elementary.
  • Forgetting to convert ΔS\Delta S from J mol1 K1\mathrm{J\ mol^{-1}\ K^{-1}} to kJ mol1 K1\mathrm{kJ\ mol^{-1}\ K^{-1}} is wrong when ΔH\Delta H is in kJ mol1\mathrm{kJ\ mol^{-1}} because units must match in ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S.
  • Reversing an electrochemical half-reaction without changing the sign of EE^\circ incorrectly treats reduction potentials as additive energies rather than intensive potentials.

Practice Questions

  1. 1 A gas sample has n=0.250 moln = 0.250\ \mathrm{mol}, T=298 KT = 298\ \mathrm{K}, and V=5.00 LV = 5.00\ \mathrm{L}. Using R=0.0821 L atm mol1 K1R = 0.0821\ \mathrm{L\ atm\ mol^{-1}\ K^{-1}}, find PP.
  2. 2 For a weak acid solution with [H+]=3.2×104 M[\mathrm{H^+}] = 3.2 \times 10^{-4}\ \mathrm{M}, calculate pH\mathrm{pH}.
  3. 3 A reaction has ΔH=45.0 kJ mol1\Delta H = -45.0\ \mathrm{kJ\ mol^{-1}} and ΔS=120 J mol1 K1\Delta S = -120\ \mathrm{J\ mol^{-1}\ K^{-1}}. Calculate ΔG\Delta G at 298 K298\ \mathrm{K} and decide whether the reaction is thermodynamically favorable.
  4. 4 Explain why increasing temperature can change both the rate of a reaction and the equilibrium position, but not for the same reason.