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E = hν
Energy of a photon. Use when calculating the energy of light from its frequency (photoelectric effect, atomic emission, spectroscopy).
c = λν
Relationship between speed of light, wavelength, and frequency. Use to convert between wavelength and frequency of electromagnetic radiation.
F ∝ (q₁q₂)/r²
Coulomb’s Law. Use to compare electrostatic attraction/repulsion between charged particles (ions, protons, electrons) based on charge and distance.
E (energy)
Energy of radiation or particles. Often calculated using E = hν in atomic/quantum problems.
ν (frequency)
Number of wave cycles per second. Used when calculating photon energy or converting with wavelength using c = λν.
λ (wavelength)
Distance between wave peaks. Used when working with electromagnetic radiation or spectral lines.
h (Planck’s constant)
Constant relating photon energy and frequency in E = hν.
c (speed of light)
Constant (2.998×10⁸ m/s) used to relate wavelength and frequency of light.
q (charge)
Electric charge of particles used in Coulombic force calculations.
r (distance)
Distance between charged particles in Coulomb’s law problems.
P₁V₁/T₁ = P₂V₂/T₂
Combined gas law. Use when a gas changes conditions (pressure, volume, temperature) but moles stay constant.
PV = nRT
Ideal gas law. Use to calculate any missing variable (P, V, n, or T) for gases under ideal conditions.
Pₐ = Ptotal × Xₐ
Partial pressure equation. Use when determining the pressure contributed by a gas in a mixture using mole fraction.
Ptotal = Pₐ + Pᵦ + …
Dalton’s Law. Use to calculate total pressure of a mixture of gases by adding individual partial pressures.
n = m / M
Mole calculation from mass. Use to convert between grams and moles in stoichiometry problems.
D = m / V
Density equation. Use when calculating density or when solving gas problems involving molar mass and density.
KE = ½mv²
Kinetic energy of moving particles. Used conceptually in kinetic molecular theory and energy calculations.
M = n / Lsolution
Molarity. Use to calculate concentration of a solution in moles per liter.
A = εbc
Beer-Lambert Law. Use in spectroscopy to relate absorbance to concentration of a solution.
P (pressure)
Force per unit area exerted by gas particles. Appears in gas law calculations.
V (volume)
Amount of space occupied by a gas or solution. Used in gas law and molarity calculations.
T (temperature)
Measure of average kinetic energy. Must be in Kelvin for gas law equations.
n (moles)
Amount of substance used in stoichiometry and gas law calculations.
X (mole fraction)
Ratio of moles of a component to total moles in a mixture. Used in partial pressure calculations.
m (mass)
Amount of matter in grams. Used in density and mole conversions.
M (molar mass)
Mass of one mole of a substance. Used to convert between grams and moles.
D (density)
Mass per volume of a substance. Used to identify substances or relate gas properties.
R (gas constant)
Constant used in the ideal gas law. Value depends on units used.
[A]t − [A]₀ = −kt
Zero-order integrated rate law. Use when reaction rate is independent of reactant concentration.
ln[A]t − ln[A]₀ = −kt
First-order integrated rate law. Use when rate depends directly on concentration of one reactant.
1/[A]t − 1/[A]₀ = kt
Second-order integrated rate law. Use when rate depends on square of concentration or two reactants.
t½ = 0.693/k
Half-life for first-order reactions. Use to determine time for concentration to drop by half.
k (rate constant)
Constant describing speed of a reaction at a given temperature.
t (time)
Time elapsed during a reaction, used in kinetics equations.
Kc = [C]ᶜ[D]ᵈ / [A]ᵃ[B]ᵇ
Equilibrium constant using molar concentrations. Use to determine extent of reaction at equilibrium.
Kp = (Pc)ᶜ(Pd)ᵈ / (Pa)ᵃ(Pb)ᵇ
Equilibrium constant using gas pressures. Used for reactions involving gases.
Kw = [H₃O⁺][OH⁻]
Ion product of water. Used to relate hydronium and hydroxide concentrations in aqueous solutions.
pH = −log[H₃O⁺]
Measure of acidity. Use when determining acidity from hydronium concentration.
pOH = −log[OH⁻]
Measure of basicity. Use when calculating base strength from hydroxide concentration.
Ka = [H₃O⁺][A⁻]/[HA]
Acid dissociation constant. Use to determine strength of weak acids.
Kb = [OH⁻][HB⁺]/[B]
Base dissociation constant. Use to determine strength of weak bases.
pKa = −log Ka
Logarithmic measure of acid strength. Lower pKa indicates stronger acid.
pKb = −log Kb
Logarithmic measure of base strength.
Kw = Ka × Kb
Relationship between conjugate acid-base pairs.
pH = pKa + log([A⁻]/[HA])
Henderson-Hasselbalch equation. Use to calculate pH of buffer solutions.
q = mcΔT
Heat transfer equation. Used in calorimetry to calculate heat absorbed or released.
ΔH°reaction = ΣΔH°f(products) − ΣΔH°f(reactants)
Standard enthalpy change of reaction calculated from formation values.
ΔS°reaction = ΣS°products − ΣS°reactants
Standard entropy change of a reaction.
ΔG°reaction = ΣΔG°f(products) − ΣΔG°f(reactants)
Standard Gibbs free energy change calculated from formation energies.
ΔG° = ΔH° − TΔS°
Used to determine spontaneity of reactions based on enthalpy and entropy.
ΔG° = −RT ln K
Connects thermodynamics and equilibrium. Use to calculate equilibrium constant from free energy.
ΔG° = −nFE°
Relationship between Gibbs free energy and electrochemical cell potential.
I = q/t
Definition of electric current. Used when calculating current from charge flow.
Ecell = E°cell − (RT/nF) ln Q
Nernst equation. Used to calculate cell potential under nonstandard conditions.
F (Faraday constant)
Charge of one mole of electrons. Used in electrochemistry calculations.
Q (reaction quotient)
Determines direction a reaction will shift relative to equilibrium.