General Chemistry: cram pack

Formula sheets, the key method steps for every topic and 14 practice problems, with full solutions at the back.

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1Formulas and methods

Stoichiometry

Moles
n = m/M
Concentration
c = n/V
Mole ratio
use the coefficients of the balanced equation
Limiting reactant
the one that runs out first
Percent yield
actual / theoretical × 100%

Method

  1. Write and balance the chemical equation.
  2. Convert the given mass to moles: n = m/M.
  3. Use the coefficients as the mole ratio to find the moles of the substance you want.
  4. Convert back to mass with m = n·M. With two reactants, find the limiting reactant first.

Molarity & dilution

Molarity
c = n/V (mol/L)
Moles
n = m/M
Dilution
c1V1 = c2V2
Mixing
c = (c1V1 + c2V2)/(V1 + V2)

Method

  1. Convert mass to moles with n = m/M.
  2. Convert the volume to litres.
  3. Molarity c = n/V in mol/L.
  4. For a dilution, the moles stay the same: c₁V₁ = c₂V₂.

Ideal gas law

Ideal gas law
pV = nRT
Gas constant
R = 8.314 J/(mol·K)
Combined gas law
p1V1/T1 = p2V2/T2
Moles
n = m/M
Temperature
T[K] = T[°C] + 273.15

Calorimetry & enthalpy

Heat
q = m·c·ΔT
Water
c = 4.18 J/(g·°C)
Calorimeter
heat lost = heat gained
Enthalpy of reaction
ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants)

Chemical equilibrium

Equilibrium constant
Kc = [C]c[D]d/([A]a[B]b)
ICE table
Initial, Change (×coefficient), Equilibrium
Quadratic
x = (−b + √(b² − 4ac))/(2a)

Method

  1. Write Kc with products over reactants, each raised to the power of its coefficient.
  2. Set up an ICE table: Initial, Change (in steps of x times the coefficients), Equilibrium.
  3. Put the equilibrium expressions into Kc and solve for x.
  4. Check whether x is small enough for an approximation; otherwise solve the quadratic.

pH & buffers

pH
pH = −log[H⁺]
pOH
pOH = −log[OH⁻], pH + pOH = 14
Weak acid
[H⁺] ≈ √(Ka·c)
Buffer
pH = pKa + log([A⁻]/[HA])
Dilution
c1V1 = c2V2

Method

  1. Decide whether the acid or base is strong (fully dissociated) or weak.
  2. Strong acid: [H⁺] equals its concentration. Strong base: find [OH⁻] first.
  3. Weak acid: solve Ka = x²/(c − x) for x = [H⁺].
  4. pH = −log[H⁺], and pH + pOH = 14 at 25 °C.

Reaction kinetics

First order
ln(CA/CA0) = −kt
Half-life (first order)
t½ = ln 2/k
Second order
1/CA = 1/CA0 + kt
Arrhenius
k = A·e−Ea/(RT)
Two temperatures
ln(k2/k1) = (Ea/R)(1/T1 − 1/T2)

2Practice problems

1.StoichiometryMedium
m(X)n(X)n(H2​O)m(H2​O)÷ M(X)× 4/ν× M(H2​O)

24 g of C3H8 and 80 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?

M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 g/mol
m = g
2.StoichiometryHard
m(Fe2​O3​)n(Fe2​O3​)n(CO2​)m(CO2​)÷ M(Fe2​O3​)× 3/1× M(CO2​)

In the reaction Fe2O3 + 3CO → 2Fe + 3CO2, 30 g of Fe2O3 reacts completely (the other reactants are in excess) and 21.83 g of CO2 is collected. Find the percent yield Y.

M(Fe2O3) = 159.69 g/molM(CO2) = 44.01 g/molactual: 21.83 g
Y = %
3.Molarity & dilutionMedium
1 mol/LV1​0.1 mol/L200 mL

You need 200 mL of 0.1 mol/L solution and have a 1 mol/L stock solution. How much water Vwater do you add to the stock solution?

c1 = 1 mol/Lc2 = 0.1 mol/LV2 = 200 mL
Vwater = mL
4.Molarity & dilutionHard
1 mol/L300 mL2.5 mol/L500 mLc = ?800 mL

300 mL of a 1 mol/L solution is mixed with 500 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 1 mol/LV1 = 300 mLc2 = 2.5 mol/LV2 = 500 mL
c = mol/L
5.Ideal gas lawMedium
320 g of O₂V = 20 LT = 15 °CP = ?

A tank of 20 L contains 320 g of O₂ at 15 °C. Treat it as an ideal gas and find the pressure P.

m = 320 gM = 32 g/molV = 20 LT = 15 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
CO₂, M = 44.01 g/molP = 300 kPaT = 200 °Cρ = ?

Find the density ρ of CO₂ at 300 kPa and 200 °C, treating it as an ideal gas.

M = 44.01 g/molP = 300 kPaT = 200 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 150 gT = 160 °Cc = 0.897 J/(g·°C)Waterm = 150 gT = 18 °Cc = 4.18 J/(g·°C)

A 150 g block of aluminium (c = 0.897 J/(g·°C)) at 160 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 18 °C in an insulated cup. Find the final temperature Tf.

mmetal = 150 gcmetal = 0.897 J/(g·°C)Tmetal = 160 °Cmwater = 150 gTwater = 18 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H2C4​H10​ + 13O₂reactants8CO₂ + 10H₂O(l)productsΔH° = ?

Use the standard enthalpies of formation to find ΔH° for the reaction 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l).

ΔH°f(C4H10) = −125.6 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
ΔH° = kJ
9.Chemical equilibriumMedium
H2​I2​HII0.20.20C−x−x+2xE0.2 − x0.2 − x2x

0.2 mol/L of H₂ and 0.2 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 36. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I100C−x+x+xE1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 1 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 1 mol/LKc = 0.05
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.01 mol/L solution of hydrofluoric acid (Ka = 0.00068).

c = 0.01 mol/LKa = 0.00068
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A buffer contains 0.25 mol/L hydrofluoric acid and 0.2 mol/L of its sodium salt. Ka = 0.00068. Find the pH pH of the buffer.

[HA] = 0.25[A⁻] = 0.2Ka = 0.00068
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)20 min0.28

In a first-order reaction the concentration of A falls from 0.8 mol/L to 0.28 mol/L in 20 min. Find the rate constant k.

CA0 = 0.8 mol/LCA = 0.28 mol/Lt = 20 min
k = min⁻¹
14.Reaction kineticsHard
Tk25 °C0.0240 °C0.0638

The rate constant of a reaction is 0.02 min⁻¹ at 25 °C and 0.0638 min⁻¹ at 40 °C. Find the activation energy Ea.

k1 = 0.02 min⁻¹T1 = 25 °Ck2 = 0.0638 min⁻¹T2 = 40 °CR = 8.314 J/(mol·K)
Ea = kJ/mol

3Solutions

1.Stoichiometry

Answer: m = 36.04 g

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Moles of each reactant

n(C3H8) = 24/44.1 = 0.5442 mol
n(O2) = 80/32 = 2.5 mol

Limiting reactant

0.5442/1 = 0.5442, 2.5/5 = 0.5 → O2

Mass of product

n(H2O) = 0.5·4 = 2 mol
m = 2·18.02 = 36.04 g

Answer

m = 36.04 g
2.Stoichiometry

Answer: Y = 88.01 %

Stoichiometry: a balanced equation counts particles, not grams. Convert mass to moles with n = m/M, use the coefficients of the equation as the mole ratio, then convert back with m = n·M. With two reactants, the limiting reactant is the one that runs out first and fixes how much product forms.

Theoretical yield

n(Fe2O3) = 30/159.69 = 0.1879 mol
m = 0.1879·3/1·44.01 = 24.8 g

Percent yield

Y = 21.83/24.8·100 = 88.01%

Answer

Y = 88.01%
3.Molarity & dilution

Answer: Vwater = 180 mL

Molarity: concentration c = n/V in mol/L, with n = m/M. Diluting adds solvent but not solute, so the number of moles stays the same: c₁·V₁ = c₂·V₂. When two solutions of the same solute are mixed, the moles add up and so do the volumes.

Volume of stock solution

V1 = c2·V2/c1 = 0.1·200/1 = 20 mL

Water to add

Vwater = 200 − 20 = 180 mL

Answer

Vwater = 180 mL
4.Molarity & dilution

Answer: c = 1.938 mol/L

Molarity: concentration c = n/V in mol/L, with n = m/M. Diluting adds solvent but not solute, so the number of moles stays the same: c₁·V₁ = c₂·V₂. When two solutions of the same solute are mixed, the moles add up and so do the volumes.

Total amount

n = 1·300 + 2.5·500 = 1550 mmol

Concentration of the mixture

c = 1550/800 = 1.938 mol/L

Answer

c = 1.938 mol/L
5.Ideal gas law

Answer: P = 1198 kPa

Ideal gas law: PV = nRT, with n = m/M.

Moles

n = m/M = 320/32 = 10 mol
T = 15 + 273.15 = 288.1 K

Pressure

P = nRT/V = 10·8.314·288.1/0.02 = 1198 kPa

Answer

P = 1198 kPa
6.Ideal gas law

Answer: ρ = 3.356 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 200 + 273.15 = 473.1 K

Density

ρ = 300·44.01/(8.314·473.1) = 3.356 kg/m³

Answer

ρ = 3.356 kg/m³
7.Calorimetry & enthalpy

Answer: Tf = 43.09 °C

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Heat balance

150·0.897·(160 − Tf) = 150·4.18·(Tf − 18)

Solve for the final temperature

Tf = (134.6·160 + 627·18)/(134.6 + 627) = 43.09 °C

Answer

Tf = 43.09 °C
8.Calorimetry & enthalpy

Answer: ΔH° = −5755 kJ

Heat and enthalpy: heating a substance takes q = m·c·ΔT. In a calorimeter the heat lost by the hot object equals the heat gained by the cold one. The enthalpy change of a reaction follows from enthalpies of formation: ΔH° = ΣΔH°f(products) − ΣΔH°f(reactants), each multiplied by its coefficient.

Enthalpy of reaction

ΔH° = [8·(−393.5) + 10·(−285.8)] − [2·(−125.6) + 13·0] = −5755 kJ

Answer

ΔH° = −5755 kJ

Negative: the reaction gives off heat (exothermic).

9.Chemical equilibrium

Answer: [HI] = 0.3 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

36 = (2x)²/(0.2 − x)²

Take the square root

6 = 2x/(0.2 − x) → x = 0.2·6/(2 + 6) = 0.15 mol/L

Equilibrium concentration

[HI] = 2x = 0.3 mol/L

Answer

[HI] = 0.3 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.2 mol/L

Chemical equilibrium: for aA + bB ⇌ cC + dD, the equilibrium constant is Kc = [C]c[D]d/([A]a[B]b), using concentrations at equilibrium. An ICE table (Initial, Change, Equilibrium) links the starting amounts to the equilibrium amounts through one unknown x, scaled by the coefficients.

Equilibrium expression

0.05 = x²/(1 − x) → x² + 0.05·x − 0.05 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.05))/2 = 0.2 mol/L

Equilibrium concentration

[Cl₂] = x = 0.2 mol/L

Answer

[Cl2] = 0.2 mol/L
11.pH & buffers

Answer: pH = 2.64

pH: pH = −log₁₀[H₃O⁺] and pOH = −log₁₀[OH⁻], with pH + pOH = 14 at 25 °C. Strong acids and bases ionise completely. A weak acid only partly: Ka = x²/(c − x), where x = [H₃O⁺]. A buffer of a weak acid and its conjugate base follows Henderson–Hasselbalch: pH = pKa + log([A⁻]/[HA]).

Equilibrium

HA ⇌ H⁺ + A⁻: x mol/L of acid ionises.

Ka = x²/(0.01 − x) → x = 0.00229 mol/L

pH

pH = −log(0.00229) = 2.64

Answer

pH = 2.64
12.pH & buffers

Answer: pH = 3.071

pH: pH = −log₁₀[H₃O⁺] and pOH = −log₁₀[OH⁻], with pH + pOH = 14 at 25 °C. Strong acids and bases ionise completely. A weak acid only partly: Ka = x²/(c − x), where x = [H₃O⁺]. A buffer of a weak acid and its conjugate base follows Henderson–Hasselbalch: pH = pKa + log([A⁻]/[HA]).

pKa

pKa = 3.167

Henderson–Hasselbalch

pH = 3.167 + log(0.2/0.25) = 3.071

Answer

pH = 3.071
13.Reaction kinetics

Answer: k = 0.05249 min⁻¹

Integrated rate laws: zero order: C = C₀ − kt (straight line, t½ = C₀/(2k)); first order: ln(C₀/C) = kt (t½ = ln 2/k); second order: 1/C − 1/C₀ = kt (t½ = 1/(kC₀)). Conversion X means C = C₀(1 − X).

Integrated first-order law

k = ln(CA0/CA)/t = ln(0.8/0.28)/20 = 1.05/20 = 0.05249 min⁻¹

Answer

k = 0.05249 min⁻¹
14.Reaction kinetics

Answer: Ea = 60.03 kJ/mol

Reaction rates: for a first-order reaction −dC/dt = kC, so C = C₀·e−kt and the half-life ln 2/k does not depend on concentration. For a second-order reaction 1/C = 1/C₀ + kt. The rate constant rises with temperature following Arrhenius: k = A·e−Ea/(RT).

Absolute temperatures

T1 = 298.1 K, T2 = 313.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·1.16/(-1.607e-4) = 60030 J/mol
Ea = 60.03 kJ/mol

Answer

Ea = 60.03 kJ/mol

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