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(MgO)m(MgO)÷ M(X)× 2/ν× M(MgO)

24 g of Mg and 10 g of O2 react according to 2Mg + O2 → 2MgO. What mass m of MgO can form?

M(Mg) = 24.31M(O2) = 32M(MgO) = 40.3 g/mol
m = g
2.StoichiometryHard
m(CH4​)n(CH4​)n(H2​O)m(H2​O)÷ M(CH4​)× 2/1× M(H2​O)

In the reaction CH4 + 2O2 → CO2 + 2H2O, 8 g of CH4 reacts completely (the other reactants are in excess) and 12.58 g of H2O is collected. Find the percent yield Y.

M(CH4) = 16.04 g/molM(H2O) = 18.02 g/molactual: 12.58 g
Y = %
3.Molarity & dilutionMedium
2 mol/LV1​ = ?0.2 mol/L1000 mL

You need 1000 mL of 0.2 mol/L solution and have a 2 mol/L stock solution. What volume V1 of stock solution do you need?

c1 = 2 mol/Lc2 = 0.2 mol/LV2 = 1000 mL
V1 = mL
4.Molarity & dilutionHard
0.5 mol/L150 mL3 mol/L200 mLc = ?350 mL

150 mL of a 0.5 mol/L solution is mixed with 200 mL of a 3 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.5 mol/LV1 = 150 mLc2 = 3 mol/LV2 = 200 mL
c = mol/L
5.Ideal gas lawMedium
230 g of ArP = 600 kPaT = 10 °CV = ?

What volume V does 230 g of Ar occupy at 600 kPa and 10 °C? Treat it as an ideal gas.

m = 230 gM = 39.95 g/molP = 600 kPaT = 10 °CR = 8.314 J/(mol·K)
V = L
6.Ideal gas lawHard
State 1State 2

A fixed amount of Ar goes from 250 kPa, 10 L, 35 °C to 550 kPa and 70 °C. Find the new volume V2.

P1 = 250 kPaV1 = 10 LT1 = 35 °CP2 = 550 kPaT2 = 70 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 50 gT = 200 °Cc = 0.897 J/(g·°C)Waterm = 100 gT = 24 °Cc = 4.18 J/(g·°C)

A 50 g block of aluminium (c = 0.897 J/(g·°C)) at 200 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 24 °C in an insulated cup. Find the final temperature Tf.

mmetal = 50 gcmetal = 0.897 J/(g·°C)Tmetal = 200 °Cmwater = 100 gTwater = 24 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H25 g C2​H6​2C2​H6​ + 7O₂reactants4CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 25 g of C2H6 (M = 30.07 g/mol) burns completely: 2C2H6 + 7O₂ → 4CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C2H6) = −84.7 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 = 64. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 64
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.100C−x+x+xE0.1 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.08 at the reaction temperature. A container starts with 0.1 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.1 mol/LKc = 0.08
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.2 mol/L solution of formic acid (Ka = 0.00018).

c = 0.2 mol/LKa = 0.00018
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.2 mol lactic acid and 0.1 mol of its conjugate base (Ka = 0.00014). 0.025 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.2 moln(A⁻) = 0.1 moln(OH⁻) = 0.025 molKa = 0.00014
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)30 minC = ?

A reaction with rate law −rA = k·CA² has k = 0.05 L/(mol·min) and starts at 0.5 mol/L. Find the concentration CA after 30 min.

k = 0.05 L/(mol·min)CA0 = 0.5 mol/Lt = 30 min
CA = mol/L
14.Reaction kineticsHard
Tk20 °C0.00560 °C?

A reaction has a rate constant of 0.005 min⁻¹ at 20 °C and an activation energy of 50 kJ/mol. Find the rate constant k2 at 60 °C.

k1 = 0.005 min⁻¹T1 = 20 °CT2 = 60 °CEa = 50 kJ/molR = 8.314 J/(mol·K)
k2 = min⁻¹

3Solutions

1.Stoichiometry

Answer: m = 25.19 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(Mg) = 24/24.31 = 0.9872 mol
n(O2) = 10/32 = 0.3125 mol

Limiting reactant

0.9872/2 = 0.4936, 0.3125/1 = 0.3125 → O2

Mass of product

n(MgO) = 0.3125·2 = 0.625 mol
m = 0.625·40.3 = 25.19 g

Answer

m = 25.19 g
2.Stoichiometry

Answer: Y = 69.99 %

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(CH4) = 8/16.04 = 0.4988 mol
m = 0.4988·2/1·18.02 = 17.98 g

Percent yield

Y = 12.58/17.98·100 = 69.99%

Answer

Y = 69.99%
3.Molarity & dilution

Answer: V1 = 100 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 = 0.2·1000/2 = 100 mL

Answer

V1 = 100 mL
4.Molarity & dilution

Answer: c = 1.929 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 = 0.5·150 + 3·200 = 675 mmol

Concentration of the mixture

c = 675/350 = 1.929 mol/L

Answer

c = 1.929 mol/L
5.Ideal gas law

Answer: V = 22.59 L

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

Moles

n = 230/39.95 = 5.757 mol
T = 10 + 273.15 = 283.1 K

Volume

V = nRT/P = 5.757·8.314·283.1/600 = 22.59 L

Answer

V = 22.59 L
6.Ideal gas law

Answer: V2 = 5.062 L

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

Absolute temperatures

T1 = 308.1 K, T2 = 343.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 10·(250/550)·(343.1/308.1) = 5.062 L

Answer

V2 = 5.062 L
7.Calorimetry & enthalpy

Answer: Tf = 41.05 °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

50·0.897·(200 − Tf) = 100·4.18·(Tf − 24)

Solve for the final temperature

Tf = (44.85·200 + 418·24)/(44.85 + 418) = 41.05 °C

Answer

Tf = 41.05 °C
8.Calorimetry & enthalpy

Answer: q = 1297 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° = [4·(−393.5) + 6·(−285.8)] − [2·(−84.7) + 7·0] = −3119 kJ

Heat for the given mass

n = 25/30.07 = 0.8314 mol
q = n·|ΔH°/2| = 0.8314·1560 = 1297 kJ

Answer

q = 1297 kJ
9.Chemical equilibrium

Answer: [HI] = 1.28 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

64 = (2x)²/(0.8 − x)²

Take the square root

8 = 2x/(0.8 − x) → x = 0.8·8/(2 + 8) = 0.64 mol/L

Equilibrium concentration

[HI] = 2x = 1.28 mol/L

Answer

[HI] = 1.28 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.05798 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/(0.1 − x) → x² + 0.08·x − 0.008 = 0

Solve the quadratic

x = (−0.08 + √(0.08² + 4·0.008))/2 = 0.05798 mol/L

Equilibrium concentration

[Cl₂] = x = 0.05798 mol/L

Answer

[Cl2] = 0.05798 mol/L
11.pH & buffers

Answer: pH = 2.228

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/(0.2 − x) → x = 0.005911 mol/L

pH

pH = −log(0.005911) = 2.228

Answer

pH = 2.228
12.pH & buffers

Answer: pH = 3.708

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 − 0.025 = 0.175 mol
n(A⁻) = 0.1 + 0.025 = 0.125 mol

Henderson–Hasselbalch

pH = 3.854 + log(0.125/0.175) = 3.708

Answer

pH = 3.708
13.Reaction kinetics

Answer: CA = 0.2857 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 + 0.05·30 = 3.5 L/mol
CA = 1/3.5 = 0.2857 mol/L

Answer

CA = 0.2857 mol/L
14.Reaction kinetics

Answer: k2 = 0.05871 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 = 293.1 K, T2 = 333.1 K

Arrhenius ratio

ln(k2/k1) = −(50000/8.314)·(1/333.1 − 1/293.1) = 2.463
k2 = 0.005·e2.463 = 0.05871 min⁻¹

Answer

k2 = 0.05871 min⁻¹

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