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Common Chemistry Formulas and Equations Cheat Sheet, Cheat Sheet of Chemistry

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Common Equations Used in Chemistry
Equation for density: d=m
v
Converting ˚F to ˚C: ˚C = (˚F - 32) x 5
9
Converting ˚C to ˚F: ˚F = ˚C x 9
5 + 32
Converting ˚C to K: K = (˚C + 273.15)
Percent composition of an element = n x molar mass of element
molar mass of compound x 100%
- where n = the number of moles of the element in one mole of the
compound
% yield = actual yield
theoretical yield x 100%
molarity (M) = moles of solute
liters of solution
Dilution of Solution: MiVi = MfVf
Boyle’s law - Constant T and n: PV = k
Boyle’s law - For calculating changes in pressure or volume: P1V1 = P2V2
Charles’ law - Constant P and n: V
T = k
Charles’ law - For calculating temperature or volume changes: V1
T1 = V2
T2
Avogadro’s law - Constant P and T: V = kn
Ideal Gas equation: PV = nRT
Calculation of changes in pressure, temperature, or volume of gas when n is
constant:
P1V1
T1 = P2V2
T2
pf3
pf4
pf5
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Common Equations Used in Chemistry

Equation for density: d=mv

Converting ˚F to ˚C: ˚C = (˚F - 32) x^59

Converting ˚C to ˚F: ˚F = ˚C x^95 + 32

Converting ˚C to K: K = (˚C + 273.15)

Percent composition of an element = n molar mass of compound^ x molar mass of element x 100%

  • where n = the number of moles of the element in one mole of the compound

% yield = (^) theoretical yieldactual yield x 100%

molarity (M) = liters of solutionmoles of solute

Dilution of Solution: Mi V (^) i = MfV (^) f Boyle’s law - Constant T and n : PV = k Boyle’s law - For calculating changes in pressure or volume: P 1 V 1 = P 2 V (^2)

Charles’ law - Constant P and n : VT = k

Charles’ law - For calculating temperature or volume changes: V T^11 = V T^22

Avogadro’s law - Constant P and T: V = k n Ideal Gas equation: PV = n RT Calculation of changes in pressure, temperature, or volume of gas when n is constant: P 1 V (^1) T 1 =

P 2 V 2

T 2

Calculation of density or molar mass of gas: d = P RT M

Dalton’s law of partial pressures - for calculating partial pressures: Pi = Xi PT

Root-mean-square speed of gas molecules: u (^) rms = (3RT M )0.

Van der waals equation; for calculating the pressure of a nonideal gas: (P + a V n^ 22 ) (V - n b) = n RT

Definition of heat capacity, where s is specific heat: C = ms Calculation of heat change in terms of specific heat : q = ms∆t Calculation of heat change in terms of heat capacity: q = C∆t

Electrical force: Fel = kq^1 rq 22

Potential energy: V = kq^1 rq^2

Calculation of standard enthalpy of reaction: ∆H ˚ rxn = ∑n∆H ˚ f (products) - ∑m ∆H ˚ f (reactants) [where n and m are coefficients in equation] Mathematical statement of the first law of thermodynamics: ∆E = q + w Work done in gas expansion or compression: w = - P∆V Definition of enthalpy: H = E + PV Enthalpy (or energy) change for a constant-pressure process: ∆H = ∆E +P∆V Enthalpy (or energy) change for a constant-pressure process: ∆E = ∆H - RT∆ n , where n is the change in the number of moles of gas.

Relationship of wavelength and frequency: u = λν

Energy of a photon: E = hν

Entropy change of heat flow at constant temperature: ∆S = Tq

Calculating the molality of a solution: molality (m) = moles of solute1000 g solvent

Henry’s law for calculating solubility (c) of gases: c = kP Raoult’s law relating the vapor pressure of a liquid to its vapor pressure in a solution: P 1 = X 1 P ˚ (^1) Vapor pressure lowering in terms of the concentration of solution: ∆P = X 2 P ˚ (^1) Boiling point elevation: ∆Tb = Kbm Freezing point depression: ∆Tf = Kfm Osmotic pressure of a solution: π = MRT The van’t Hoff factor for an electrolyte solution: i = actual number of particles in soln after dissociationnumber of formula units initially dissoved in soln

Rate law expression. The sum (x+ y) gives the overall order of the reaction: rate = k[A]x[B]y Relationship between concentration and time for a first-order reaction: ln [A]o [A] = kt Equation for the graphical determination of k for a first-order reaction: ln [A] = -kt + ln [A]o

Half-life for a first-order reaction: t1/2 = ln 2k = 0.693k

Relationship between concentration and time for a second-order reaction: (^) [A]^1 = (^) [A]o^1 + kt

The Arrhenius equation expressing the dependence of the rate constant on activation energy and temperature: k = Ae-Ea/RT

Equation for the graphical determination of activation energy: ln k = (- E Ra ) (T^1 ) + ln A

Relationships of rate constants at two different temperatures: ln k k^12 = Ea R (

T 1 - T 2

T 1 T 2 )

Law of Mass Action - General expression of equilibrium constant: K = [A][C]ca[D][B]db

Relationship between Kp and Kc: Kp = Kc(0.0821*T)∆n The equilibrium constant for the overall reaction is given by the product of the equilibrium constants for the individual reactions: Kc = K’cK”c Ion-product constant of water: Kw = [H+][OH-]

Definition of pH of a solution: pH = -log [H+]

Definition of pOH of a solution: pOH = -log [OH-] Another form of ion-product constant of water: pH + pOH = 14.

Percent ionization = ionized acid concentration at equilibriuminitial concentration of acid x 100%

Relationship between the acid and base ionization constants of a conjugate acid-base pair: KaKb = Kw

Henderson-Hasselbach equation: pH = pKa + log [conjugate base][acid]

The second law of thermodynamics (spontaneous process): ∆Suniv = ∆Ssys +∆Ssurr > 0 The second law of thermodynamics (equilibrium process): ∆Suniv = ∆Ssys + ∆Ssurr = 0