General Chemistry: cram pack

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

New problemsBack to the course

In the print window, choose “Save as PDF” to keep a copy on your device.

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)

10 g of C3H8 and 8 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(Na)n(Na)n(NaCl)m(NaCl)÷ M(Na)× 2/2× M(NaCl)

In the reaction 2Na + Cl2 → 2NaCl, 8 g of Na reacts completely (the other reactants are in excess) and 18.51 g of NaCl is collected. Find the percent yield Y.

M(Na) = 22.99 g/molM(NaCl) = 58.44 g/molactual: 18.51 g
Y = %
3.Molarity & dilutionMedium
2.5 mol/LV1​0.25 mol/L500 mL

You need 500 mL of 0.25 mol/L solution and have a 2.5 mol/L stock solution. How much water Vwater do you add to the stock solution?

c1 = 2.5 mol/Lc2 = 0.25 mol/LV2 = 500 mL
Vwater = mL
4.Molarity & dilutionHard
0.8 mol/L50 mL0.1 mol/L100 mLc = ?150 mL

50 mL of a 0.8 mol/L solution is mixed with 100 mL of a 0.1 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.8 mol/LV1 = 50 mLc2 = 0.1 mol/LV2 = 100 mL
c = mol/L
5.Ideal gas lawMedium
210 g of HeP = 500 kPaT = 15 °CV = ?

What volume V does 210 g of He occupy at 500 kPa and 15 °C? Treat it as an ideal gas.

m = 210 gM = 4.003 g/molP = 500 kPaT = 15 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of CH₄ goes from 250 kPa, 5 L, 20 °C to 500 kPa and 120 °C. Find the new volume V2.

P1 = 250 kPaV1 = 5 LT1 = 20 °CP2 = 500 kPaT2 = 120 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Leadm = 200 gT = 150 °Cc = 0.129 J/(g·°C)Waterm = 200 gT = 17 °Cc = 4.18 J/(g·°C)

A 200 g block of lead (c = 0.129 J/(g·°C)) at 150 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 17 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.129 J/(g·°C)Tmetal = 150 °Cmwater = 200 gTwater = 17 °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​HII0.20.20C−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 = 9. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.2500C−x+x+xE0.25 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.25 mol/LKc = 0.2
[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 0.3 mol hydrofluoric acid and 0.25 mol of its conjugate base (Ka = 0.00068). 0.01 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.3 moln(A⁻) = 0.25 moln(OH⁻) = 0.01 molKa = 0.00068
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)t½​ = ?C0​/2

A second-order reaction (−rA = k·CA²) has k = 0.02 L/(mol·min) and an initial concentration of 1.5 mol/L. Find its first half-life t½.

k = 0.02 L/(mol·min)CA0 = 1.5 mol/L
t½ = min
14.Reaction kineticsHard
Tk20 °C0.0130 °C0.0258

The rate constant of a reaction is 0.01 min⁻¹ at 20 °C and 0.0258 min⁻¹ at 30 °C. Find the activation energy Ea.

k1 = 0.01 min⁻¹T1 = 20 °Ck2 = 0.0258 min⁻¹T2 = 30 °CR = 8.314 J/(mol·K)
Ea = kJ/mol

3Solutions

1.Stoichiometry

Answer: m = 3.604 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) = 10/44.1 = 0.2268 mol
n(O2) = 8/32 = 0.25 mol

Limiting reactant

0.2268/1 = 0.2268, 0.25/5 = 0.05 → O2

Mass of product

n(H2O) = 0.05·4 = 0.2 mol
m = 0.2·18.02 = 3.604 g

Answer

m = 3.604 g
2.Stoichiometry

Answer: Y = 91.02 %

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) = 8/22.99 = 0.348 mol
m = 0.348·2/2·58.44 = 20.34 g

Percent yield

Y = 18.51/20.34·100 = 91.02%

Answer

Y = 91.02%
3.Molarity & dilution

Answer: Vwater = 450 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 = 0.25·500/2.5 = 50 mL

Water to add

Vwater = 500 − 50 = 450 mL

Answer

Vwater = 450 mL
4.Molarity & dilution

Answer: c = 0.3333 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 = 0.8·50 + 0.1·100 = 50 mmol

Concentration of the mixture

c = 50/150 = 0.3333 mol/L

Answer

c = 0.3333 mol/L
5.Ideal gas law

Answer: V = 251.4 L

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

Moles

n = 210/4.003 = 52.46 mol
T = 15 + 273.15 = 288.1 K

Volume

V = nRT/P = 52.46·8.314·288.1/500 = 251.4 L

Answer

V = 251.4 L
6.Ideal gas law

Answer: V2 = 3.353 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 393.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(250/500)·(393.1/293.1) = 3.353 L

Answer

V2 = 3.353 L
7.Calorimetry & enthalpy

Answer: Tf = 20.98 °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

200·0.129·(150 − Tf) = 200·4.18·(Tf − 17)

Solve for the final temperature

Tf = (25.8·150 + 836·17)/(25.8 + 836) = 20.98 °C

Answer

Tf = 20.98 °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] = 0.08 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

9 = (2x)²/(0.2 − x)²

Take the square root

3 = 2x/(0.2 − x) → x = 0.2·3/(2 + 3) = 0.12 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.08 mol/L

Answer

[H2] = 0.08 mol/L
10.Chemical equilibrium

Answer: [PCl5] = 0.1051 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

0.2 = x²/(0.25 − x) → x² + 0.2·x − 0.05 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.05))/2 = 0.1449 mol/L

Equilibrium concentration

[PCl₅] = 0.25 − 0.1449 = 0.1051 mol/L

Answer

[PCl5] = 0.1051 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 = 3.12

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) = 0.3 − 0.01 = 0.29 mol
n(A⁻) = 0.25 + 0.01 = 0.26 mol

Henderson–Hasselbalch

pH = 3.167 + log(0.26/0.29) = 3.12

Answer

pH = 3.12
13.Reaction kinetics

Answer: t½ = 33.33 min

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).

Second-order half-life

t½ = 1/(k·CA0) = 1/(0.02·1.5) = 33.33 min

Answer

t½ = 33.33 min

Each later half-life is twice as long, because C₀ has halved.

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

ExamProblems · examproblems.com/courses/general-chemistry