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)

6 g of H2 and 8 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(CaCO3​)n(CaCO3​)n(CaO)m(CaO)÷ M(CaCO3​)× 1/1× M(CaO)

In the reaction CaCO3 → CaO + CO2, 10 g of CaCO3 reacts completely (the other reactants are in excess) and 5.27 g of CaO is collected. Find the percent yield Y.

M(CaCO3) = 100.09 g/molM(CaO) = 56.08 g/molactual: 5.27 g
Y = %
3.Molarity & dilutionMedium
4 mol/LV1​ = ?0.2 mol/L1000 mL

You need 1000 mL of 0.2 mol/L solution and have a 4 mol/L stock solution. What volume V1 of stock solution do you need?

c1 = 4 mol/Lc2 = 0.2 mol/LV2 = 1000 mL
V1 = mL
4.Molarity & dilutionHard
0.1 mol/L250 mL2.5 mol/L100 mLc = ?350 mL

250 mL of a 0.1 mol/L solution is mixed with 100 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.1 mol/LV1 = 250 mLc2 = 2.5 mol/LV2 = 100 mL
c = mol/L
5.Ideal gas lawMedium
220 g of CH₄V = 10 LT = 10 °CP = ?

A tank of 10 L contains 220 g of CH₄ at 10 °C. Treat it as an ideal gas and find the pressure P.

m = 220 gM = 16.04 g/molV = 10 LT = 10 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of Ar goes from 300 kPa, 2 L, 20 °C to 600 kPa and 250 °C. Find the new volume V2.

P1 = 300 kPaV1 = 2 LT1 = 20 °CP2 = 600 kPaT2 = 250 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Copperm = 200 gT = 140 °Cc = 0.385 J/(g·°C)Waterm = 150 gT = 20 °Cc = 4.18 J/(g·°C)

A 200 g block of copper (c = 0.385 J/(g·°C)) at 140 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 20 °C in an insulated cup. Find the final temperature Tf.

mmetal = 200 gcmetal = 0.385 J/(g·°C)Tmetal = 140 °Cmwater = 150 gTwater = 20 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H50 g CH4​CH4​ + 2O₂reactantsCO₂ + 2H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 50 g of CH4 (M = 16.04 g/mol) burns completely: CH4 + 2O₂ → CO₂ + 2H₂O(l). Give q as a positive number.

ΔH°f(CH4) = −74.8 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 = 16. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 16
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].

[PCl₅]₀ = 0.1 mol/LKc = 0.2
[PCl5] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.05 mol/L solution of acetic acid (Ka = 1.8 × 10⁻⁵).

c = 0.05 mol/LKa = 1.8 × 10⁻⁵
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.2 mol formic acid and 0.25 mol of its conjugate base (Ka = 0.00018). 0.01 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.2 moln(A⁻) = 0.25 moln(OH⁻) = 0.01 molKa = 0.00018
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)20 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.4 L/(mol·min) and starts at 0.5 mol/L. Find the concentration CA after 20 min.

k = 0.4 L/(mol·min)CA0 = 0.5 mol/Lt = 20 min
CA = mol/L
14.Reaction kineticsHard
Tk35 °C0.00545 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 35 °C and an activation energy of 90 kJ/mol. Find the rate constant k2 at 45 °C.

k1 = 0.005 min⁻¹T1 = 35 °CT2 = 45 °CEa = 90 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹

3Solutions

1.Stoichiometry

Answer: m = 9.01 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) = 6/2.016 = 2.976 mol
n(O2) = 8/32 = 0.25 mol

Limiting reactant

2.976/2 = 1.488, 0.25/1 = 0.25 → O2

Mass of product

n(H2O) = 0.25·2 = 0.5 mol
m = 0.5·18.02 = 9.01 g

Answer

m = 9.01 g
2.Stoichiometry

Answer: Y = 94.06 %

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(CaCO3) = 10/100.09 = 0.09991 mol
m = 0.09991·1/1·56.08 = 5.603 g

Percent yield

Y = 5.27/5.603·100 = 94.06%

Answer

Y = 94.06%
3.Molarity & dilution

Answer: V1 = 50 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 = 0.2·1000/4 = 50 mL

Answer

V1 = 50 mL
4.Molarity & dilution

Answer: c = 0.7857 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 = 0.1·250 + 2.5·100 = 275 mmol

Concentration of the mixture

c = 275/350 = 0.7857 mol/L

Answer

c = 0.7857 mol/L
5.Ideal gas law

Answer: P = 3229 kPa

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

Moles

n = m/M = 220/16.04 = 13.72 mol
T = 10 + 273.15 = 283.1 K

Pressure

P = nRT/V = 13.72·8.314·283.1/0.01 = 3229 kPa

Answer

P = 3229 kPa
6.Ideal gas law

Answer: V2 = 1.785 L

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

Absolute temperatures

T1 = 293.1 K, T2 = 523.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 2·(300/600)·(523.1/293.1) = 1.785 L

Answer

V2 = 1.785 L
7.Calorimetry & enthalpy

Answer: Tf = 33.13 °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

200·0.385·(140 − Tf) = 150·4.18·(Tf − 20)

Solve for the final temperature

Tf = (77·140 + 627·20)/(77 + 627) = 33.13 °C

Answer

Tf = 33.13 °C
8.Calorimetry & enthalpy

Answer: q = 2775 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° = [1·(−393.5) + 2·(−285.8)] − [1·(−74.8) + 2·0] = −890.3 kJ

Heat for the given mass

n = 50/16.04 = 3.117 mol
q = n·|ΔH°/1| = 3.117·890.3 = 2775 kJ

Answer

q = 2775 kJ
9.Chemical equilibrium

Answer: [HI] = 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/(0.2 − x)²

Take the square root

4 = 2x/(0.2 − x) → x = 0.2·4/(2 + 4) = 0.1333 mol/L

Equilibrium concentration

[HI] = 2x = 0.2667 mol/L

Answer

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

Answer: [PCl5] = 0.02679 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/(0.1 − x) → x² + 0.2·x − 0.02 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.02))/2 = 0.07321 mol/L

Equilibrium concentration

[PCl₅] = 0.1 − 0.07321 = 0.02679 mol/L

Answer

[PCl5] = 0.02679 mol/L
11.pH & buffers

Answer: pH = 3.027

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/(0.05 − x) → x = 0.0009397 mol/L

pH

pH = −log(0.0009397) = 3.027

Answer

pH = 3.027
12.pH & buffers

Answer: pH = 3.881

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) = 0.2 − 0.01 = 0.19 mol
n(A⁻) = 0.25 + 0.01 = 0.26 mol

Henderson–Hasselbalch

pH = 3.745 + log(0.26/0.19) = 3.881

Answer

pH = 3.881
13.Reaction kinetics

Answer: CA = 0.1 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 = 2 + 0.4·20 = 10 L/mol
CA = 1/10 = 0.1 mol/L

Answer

CA = 0.1 mol/L
14.Reaction kinetics

Answer: k2 = 0.01508 min⁻¹

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 = 308.1 K, T2 = 318.1 K

Arrhenius ratio

ln(k2/k1) = −(90000/8.314)·(1/318.1 − 1/308.1) = 1.104
k2 = 0.005·e1.104 = 0.01508 min⁻¹

Answer

k2 = 0.01508 min⁻¹

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