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)× 2/ν× M(H2​O)

12 g of H2 and 24 g of O2 react according to 2H2 + O2 → 2H2O. What mass m of H2O can form?

M(H2) = 2.016M(O2) = 32M(H2O) = 18.02 g/mol
m = g
2.StoichiometryHard
m(Na)n(Na)n(NaCl)m(NaCl)÷ M(Na)× 2/2× M(NaCl)

In the reaction 2Na + Cl2 → 2NaCl, 10 g of Na reacts completely (the other reactants are in excess) and 19.06 g of NaCl is collected. Find the percent yield Y.

M(Na) = 22.99 g/molM(NaCl) = 58.44 g/molactual: 19.06 g
Y = %
3.Molarity & dilutionMedium
0.5 mol/LV1​0.4 mol/L1000 mL

You need 1000 mL of 0.4 mol/L solution and have a 0.5 mol/L stock solution. How much water Vwater do you add to the stock solution?

c1 = 0.5 mol/Lc2 = 0.4 mol/LV2 = 1000 mL
Vwater = mL
4.Molarity & dilutionHard
1 mol/L300 mL1.2 mol/L200 mLc = ?500 mL

300 mL of a 1 mol/L solution is mixed with 200 mL of a 1.2 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 1 mol/LV1 = 300 mLc2 = 1.2 mol/LV2 = 200 mL
c = mol/L
5.Ideal gas lawMedium
500 g of N₂P = 150 kPaT = 5 °CV = ?

What volume V does 500 g of N₂ occupy at 150 kPa and 5 °C? Treat it as an ideal gas.

m = 500 gM = 28.01 g/molP = 150 kPaT = 5 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of O₂ goes from 150 kPa, 5 L, 25 °C to 250 kPa and 160 °C. Find the new volume V2.

P1 = 150 kPaV1 = 5 LT1 = 25 °CP2 = 250 kPaT2 = 160 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Zincm = 100 gT = 200 °Cc = 0.388 J/(g·°C)Waterm = 200 gT = 20 °Cc = 4.18 J/(g·°C)

A 100 g block of zinc (c = 0.388 J/(g·°C)) at 200 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 100 gcmetal = 0.388 J/(g·°C)Tmetal = 200 °Cmwater = 200 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H50 g C2​H5​OHC2​H5​OH + 3O₂reactants2CO₂ + 3H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of C2H5OH (M = 46.07 g/mol) burns completely: C2H5OH + 3O₂ → 2CO₂ + 3H₂O(l). Give q as a positive number.

ΔH°f(C2H5OH) = −277.7 kJ/molΔH°f(CO₂) = −393.5 kJ/molΔH°f(H₂O, l) = −285.8 kJ/molΔH°f(O₂) = 0
q = kJ
9.Chemical equilibriumMedium
H2​I2​HII0.80.80C−x−x+2xE0.8 − x0.8 − x2x

0.8 mol/L of H₂ and 0.8 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.5 mol/LKc = 0.08
[PCl5] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.01 mol/L solution of benzoic acid (Ka = 6.3 × 10⁻⁵).

c = 0.01 mol/LKa = 6.3 × 10⁻⁵
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.25 mol acetic acid and 0.15 mol of its conjugate base (Ka = 1.8 × 10⁻⁵). 0.025 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.25 moln(A⁻) = 0.15 moln(OH⁻) = 0.025 molKa = 1.8 × 10⁻⁵
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)5 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.4 L/(mol·min) and starts at 2 mol/L. Find the concentration CA after 5 min.

k = 0.4 L/(mol·min)CA0 = 2 mol/Lt = 5 min
CA = mol/L
14.Reaction kineticsHard
Tk20 °C0.0530 °C0.129

The rate constant of a reaction is 0.05 min⁻¹ at 20 °C and 0.129 min⁻¹ at 30 °C. Find the activation energy Ea.

k1 = 0.05 min⁻¹T1 = 20 °Ck2 = 0.129 min⁻¹T2 = 30 °CR = 8.314 J/(mol·K)
Ea = kJ/mol

3Solutions

1.Stoichiometry

Answer: m = 27.03 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(H2) = 12/2.016 = 5.952 mol
n(O2) = 24/32 = 0.75 mol

Limiting reactant

5.952/2 = 2.976, 0.75/1 = 0.75 → O2

Mass of product

n(H2O) = 0.75·2 = 1.5 mol
m = 1.5·18.02 = 27.03 g

Answer

m = 27.03 g
2.Stoichiometry

Answer: Y = 74.98 %

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(Na) = 10/22.99 = 0.435 mol
m = 0.435·2/2·58.44 = 25.42 g

Percent yield

Y = 19.06/25.42·100 = 74.98%

Answer

Y = 74.98%
3.Molarity & dilution

Answer: Vwater = 200 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 = 0.4·1000/0.5 = 800 mL

Water to add

Vwater = 1000 − 800 = 200 mL

Answer

Vwater = 200 mL
4.Molarity & dilution

Answer: c = 1.08 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 + 1.2·200 = 540 mmol

Concentration of the mixture

c = 540/500 = 1.08 mol/L

Answer

c = 1.08 mol/L
5.Ideal gas law

Answer: V = 275.2 L

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

Moles

n = 500/28.01 = 17.85 mol
T = 5 + 273.15 = 278.1 K

Volume

V = nRT/P = 17.85·8.314·278.1/150 = 275.2 L

Answer

V = 275.2 L
6.Ideal gas law

Answer: V2 = 4.358 L

Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.

Absolute temperatures

T1 = 298.1 K, T2 = 433.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(150/250)·(433.1/298.1) = 4.358 L

Answer

V2 = 4.358 L
7.Calorimetry & enthalpy

Answer: Tf = 27.98 °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

100·0.388·(200 − Tf) = 200·4.18·(Tf − 20)

Solve for the final temperature

Tf = (38.8·200 + 836·20)/(38.8 + 836) = 27.98 °C

Answer

Tf = 27.98 °C
8.Calorimetry & enthalpy

Answer: q = 1483 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° = [2·(−393.5) + 3·(−285.8)] − [1·(−277.7) + 3·0] = −1367 kJ

Heat for the given mass

n = 50/46.07 = 1.085 mol
q = n·|ΔH°/1| = 1.085·1367 = 1483 kJ

Answer

q = 1483 kJ
9.Chemical equilibrium

Answer: [H2] = 0.2667 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

16 = (2x)²/(0.8 − x)²

Take the square root

4 = 2x/(0.8 − x) → x = 0.8·4/(2 + 4) = 0.5333 mol/L

Equilibrium concentration

[H₂] = 0.8 − x = 0.2667 mol/L

Answer

[H2] = 0.2667 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.336 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

0.08 = x²/(0.5 − x) → x² + 0.08·x − 0.04 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.04))/2 = 0.164 mol/L

Equilibrium concentration

[PCl₅] = 0.5 − 0.164 = 0.336 mol/L

Answer

[PCl5] = 0.336 mol/L
11.pH & buffers

Answer: pH = 3.118

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 = 0.0007629 mol/L

pH

pH = −log(0.0007629) = 3.118

Answer

pH = 3.118
12.pH & buffers

Answer: pH = 4.636

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]).

Neutralisation

n(HA) = 0.25 − 0.025 = 0.225 mol
n(A⁻) = 0.15 + 0.025 = 0.175 mol

Henderson–Hasselbalch

pH = 4.745 + log(0.175/0.225) = 4.636

Answer

pH = 4.636
13.Reaction kinetics

Answer: CA = 0.4 mol/L

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).

Integrated second-order law

1/CA = 1/CA0 + kt = 0.5 + 0.4·5 = 2.5 L/mol
CA = 1/2.5 = 0.4 mol/L

Answer

CA = 0.4 mol/L
14.Reaction kinetics

Answer: Ea = 70.03 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 = 293.1 K, T2 = 303.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·0.9478/(-1.125e-4) = 70028 J/mol
Ea = 70.03 kJ/mol

Answer

Ea = 70.03 kJ/mol

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