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(CO2​)m(CO2​)÷ M(X)× 1/ν× M(CO2​)

4 g of CH4 and 16 g of O2 react according to CH4 + 2O2 → CO2 + 2H2O. What mass m of CO2 can form?

M(CH4) = 16.04M(O2) = 32M(CO2) = 44.01 g/mol
m = g
2.StoichiometryHard
m(C3​H8​)n(C3​H8​)n(H2​O)m(H2​O)÷ M(C3​H8​)× 4/1× M(H2​O)

In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 30 g of C3H8 reacts completely (the other reactants are in excess) and 30.4 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 30.4 g
Y = %
3.Molarity & dilutionMedium
4 mol/LV1​0.25 mol/L200 mL

You need 200 mL of 0.25 mol/L solution and have a 4 mol/L stock solution. How much water Vwater do you add to the stock solution?

c1 = 4 mol/Lc2 = 0.25 mol/LV2 = 200 mL
Vwater = mL
4.Molarity & dilutionHard
0.8 mol/L50 mL0.3 mol/L250 mLc = ?300 mL

50 mL of a 0.8 mol/L solution is mixed with 250 mL of a 0.3 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.8 mol/LV1 = 50 mLc2 = 0.3 mol/LV2 = 250 mL
c = mol/L
5.Ideal gas lawMedium
250 g of N₂V = 50 LT = 15 °CP = ?

A tank of 50 L contains 250 g of N₂ at 15 °C. Treat it as an ideal gas and find the pressure P.

m = 250 gM = 28.01 g/molV = 50 LT = 15 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
He, M = 4.003 g/molP = 800 kPaT = 140 °Cρ = ?

Find the density ρ of He at 800 kPa and 140 °C, treating it as an ideal gas.

M = 4.003 g/molP = 800 kPaT = 140 °CR = 8.314 J/(mol·K)
ρ = kg/m³
7.Calorimetry & enthalpyMedium
Tf​ = ?Ironm = 75 gT = 130 °Cc = 0.449 J/(g·°C)Waterm = 400 gT = 23 °Cc = 4.18 J/(g·°C)

A 75 g block of iron (c = 0.449 J/(g·°C)) at 130 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 23 °C in an insulated cup. Find the final temperature Tf.

mmetal = 75 gcmetal = 0.449 J/(g·°C)Tmetal = 130 °Cmwater = 400 gTwater = 23 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H10 g C6​H12​O6​C6​H12​O6​ + 6O₂reactants6CO₂ + 6H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 10 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.

ΔH°f(C6H12O6) = −1274 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 = 4. Find the equilibrium concentration [H2].

[H₂]₀ = [I₂]₀ = 0.2 mol/LKc = 4
[H2] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.2500C−x+x+xE0.25 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 0.25 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.25 mol/LKc = 0.05
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.01 mol/L solution of lactic acid (Ka = 0.00014).

c = 0.01 mol/LKa = 0.00014
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.1 mol formic acid and 0.1 mol of its conjugate base (Ka = 0.00018). 0.01 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.1 moln(A⁻) = 0.1 moln(OH⁻) = 0.01 molKa = 0.00018
pH =
13.Reaction kineticsMedium
t (min)X (%)t = ?90%

A first-order reaction in a batch reactor has k = 0.1 min⁻¹. How long does it take to reach 90% conversion? Find t.

k = 0.1 min⁻¹X = 90 %
t = min
14.Reaction kineticsHard
Tk20 °Ck1​?4·k1​

A reaction has an activation energy of 55 kJ/mol. At 20 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 4 times faster?

Ea = 55 kJ/molT1 = 20 °Ck2/k1 = 4R = 8.314 J/(mol·K)
T2 = °C

3Solutions

1.Stoichiometry

Answer: m = 10.98 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(CH4) = 4/16.04 = 0.2494 mol
n(O2) = 16/32 = 0.5 mol

Limiting reactant

0.2494/1 = 0.2494, 0.5/2 = 0.25 → CH4

Mass of product

n(CO2) = 0.2494·1 = 0.2494 mol
m = 0.2494·44.01 = 10.98 g

Answer

m = 10.98 g
2.Stoichiometry

Answer: Y = 62 %

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(C3H8) = 30/44.1 = 0.6803 mol
m = 0.6803·4/1·18.02 = 49.03 g

Percent yield

Y = 30.4/49.03·100 = 62%

Answer

Y = 62%
3.Molarity & dilution

Answer: Vwater = 187.5 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 = 0.25·200/4 = 12.5 mL

Water to add

Vwater = 200 − 12.5 = 187.5 mL

Answer

Vwater = 187.5 mL
4.Molarity & dilution

Answer: c = 0.3833 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 + 0.3·250 = 115 mmol

Concentration of the mixture

c = 115/300 = 0.3833 mol/L

Answer

c = 0.3833 mol/L
5.Ideal gas law

Answer: P = 427.6 kPa

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

Moles

n = m/M = 250/28.01 = 8.925 mol
T = 15 + 273.15 = 288.1 K

Pressure

P = nRT/V = 8.925·8.314·288.1/0.05 = 427.6 kPa

Answer

P = 427.6 kPa
6.Ideal gas law

Answer: ρ = 0.9323 kg/m³

Ideal gas density: ρ = PM/(RT).

Rearrange the gas law

PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 140 + 273.15 = 413.1 K

Density

ρ = 800·4.003/(8.314·413.1) = 0.9323 kg/m³

Answer

ρ = 0.9323 kg/m³
7.Calorimetry & enthalpy

Answer: Tf = 25.11 °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

75·0.449·(130 − Tf) = 400·4.18·(Tf − 23)

Solve for the final temperature

Tf = (33.68·130 + 1672·23)/(33.68 + 1672) = 25.11 °C

Answer

Tf = 25.11 °C
8.Calorimetry & enthalpy

Answer: q = 155.5 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° = [6·(−393.5) + 6·(−285.8)] − [1·(−1274) + 6·0] = −2802 kJ

Heat for the given mass

n = 10/180.16 = 0.05551 mol
q = n·|ΔH°/1| = 0.05551·2802 = 155.5 kJ

Answer

q = 155.5 kJ
9.Chemical equilibrium

Answer: [H2] = 0.1 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

4 = (2x)²/(0.2 − x)²

Take the square root

2 = 2x/(0.2 − x) → x = 0.2·2/(2 + 2) = 0.1 mol/L

Equilibrium concentration

[H₂] = 0.2 − x = 0.1 mol/L

Answer

[H2] = 0.1 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.08956 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/(0.25 − x) → x² + 0.05·x − 0.0125 = 0

Solve the quadratic

x = (−0.05 + √(0.05² + 4·0.0125))/2 = 0.08956 mol/L

Equilibrium concentration

[Cl₂] = x = 0.08956 mol/L

Answer

[Cl2] = 0.08956 mol/L
11.pH & buffers

Answer: pH = 2.953

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 = 0.001115 mol/L

pH

pH = −log(0.001115) = 2.953

Answer

pH = 2.953
12.pH & buffers

Answer: pH = 3.832

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) = 0.1 − 0.01 = 0.09 mol
n(A⁻) = 0.1 + 0.01 = 0.11 mol

Henderson–Hasselbalch

pH = 3.745 + log(0.11/0.09) = 3.832

Answer

pH = 3.832
13.Reaction kinetics

Answer: t = 23.03 min

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).

Conversion and concentration

C/C0 = 1 − X = 0.1

Solve for the time

t = −ln(1 − X)/k = −ln(0.1)/0.1 = 23.03 min

Answer

t = 23.03 min
14.Reaction kinetics

Answer: T2 = 39.19 °C

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 temperature

T1 = 293.1 K

Solve Arrhenius for T₂

1/T2 = 1/293.1 − 8.314·ln(4)/55000 = 3.411 × 10⁻³ − 2.096 × 10⁻⁴ = 3.202 × 10⁻³ K⁻¹
T2 = 312.3 K = 39.19 °C

Answer

T2 = 39.19 °C

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