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(NH3​)m(NH3​)÷ M(X)× 2/ν× M(NH3​)

30 g of N2 and 40 g of H2 react according to N2 + 3H2 → 2NH3. What mass m of NH3 can form?

M(N2) = 28.02M(H2) = 2.016M(NH3) = 17.03 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, 12 g of C3H8 reacts completely (the other reactants are in excess) and 16.67 g of H2O is collected. Find the percent yield Y.

M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 16.67 g
Y = %
3.Molarity & dilutionMedium
0.5 mol/LV1​0.25 mol/L250 mL

You need 250 mL of 0.25 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 = 0.25 mol/LV2 = 250 mL
Vwater = mL
4.Molarity & dilutionHard
0.2 mol/L300 mL0.1 mol/L50 mLc = ?350 mL

300 mL of a 0.2 mol/L solution is mixed with 50 mL of a 0.1 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).

c1 = 0.2 mol/LV1 = 300 mLc2 = 0.1 mol/LV2 = 50 mL
c = mol/L
5.Ideal gas lawMedium
40 g of N₂V = 20 LT = 25 °CP = ?

A tank of 20 L contains 40 g of N₂ at 25 °C. Treat it as an ideal gas and find the pressure P.

m = 40 gM = 28.01 g/molV = 20 LT = 25 °CR = 8.314 J/(mol·K)
P = kPa
6.Ideal gas lawHard
State 1State 2

A fixed amount of N₂ goes from 350 kPa, 5 L, 10 °C to 450 kPa and 220 °C. Find the new volume V2.

P1 = 350 kPaV1 = 5 LT1 = 10 °CP2 = 450 kPaT2 = 220 °C
V2 = L
7.Calorimetry & enthalpyMedium
Tf​ = ?Aluminiumm = 75 gT = 120 °Cc = 0.897 J/(g·°C)Waterm = 250 gT = 24 °Cc = 4.18 J/(g·°C)

A 75 g block of aluminium (c = 0.897 J/(g·°C)) at 120 °C is dropped into 250 g of water (c = 4.18 J/(g·°C)) at 24 °C in an insulated cup. Find the final temperature Tf.

mmetal = 75 gcmetal = 0.897 J/(g·°C)Tmetal = 120 °Cmwater = 250 gTwater = 24 °Ccwater = 4.18 J/(g·°C)
Tf = °C
8.Calorimetry & enthalpyHard
H250 g CH3​OH2CH3​OH + 3O₂reactants2CO₂ + 4H₂O(l)productsq = ?

Use the standard enthalpies of formation to find the heat q released when 250 g of CH3OH (M = 32.04 g/mol) burns completely: 2CH3OH + 3O₂ → 2CO₂ + 4H₂O(l). Give q as a positive number.

ΔH°f(CH3OH) = −238.7 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​HII0.40.40C−x−x+2xE0.4 − x0.4 − x2x

0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 36. Find the equilibrium concentration [HI].

[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 36
[HI] = mol/L
10.Chemical equilibriumHard
PCl5​PCl3​Cl2​I0.500C−x+x+xE0.5 − xxx

PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].

[PCl₅]₀ = 0.5 mol/LKc = 0.2
[Cl2] = mol/L
11.pH & buffersMedium
02468101214acidicneutralbasicpH = ?

Find the pH pH of a 0.5 mol/L solution of benzoic acid (Ka = 6.3 × 10⁻⁵).

c = 0.5 mol/LKa = 6.3 × 10⁻⁵
pH =
12.pH & buffersHard
02468101214acidicneutralbasicpH = ?

A 1.00 L buffer contains 0.3 mol formic acid and 0.15 mol of its conjugate base (Ka = 0.00018). 0.025 mol of NaOH is added. Find the new pH pH.

n(HA) = 0.3 moln(A⁻) = 0.15 moln(OH⁻) = 0.025 molKa = 0.00018
pH =
13.Reaction kineticsMedium
t (min)C (mol/L)60 min0.6

In a first-order reaction the concentration of A falls from 1 mol/L to 0.6 mol/L in 60 min. Find the rate constant k.

CA0 = 1 mol/LCA = 0.6 mol/Lt = 60 min
k = min⁻¹
14.Reaction kineticsHard
Tk35 °C0.00260 °C0.0155

The rate constant of a reaction is 0.002 min⁻¹ at 35 °C and 0.0155 min⁻¹ at 60 °C. Find the activation energy Ea.

k1 = 0.002 min⁻¹T1 = 35 °Ck2 = 0.0155 min⁻¹T2 = 60 °CR = 8.314 J/(mol·K)
Ea = kJ/mol

3Solutions

1.Stoichiometry

Answer: m = 36.47 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(N2) = 30/28.02 = 1.071 mol
n(H2) = 40/2.016 = 19.84 mol

Limiting reactant

1.071/1 = 1.071, 19.84/3 = 6.614 → N2

Mass of product

n(NH3) = 1.071·2 = 2.141 mol
m = 2.141·17.03 = 36.47 g

Answer

m = 36.47 g
2.Stoichiometry

Answer: Y = 84.99 %

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(C3H8) = 12/44.1 = 0.2721 mol
m = 0.2721·4/1·18.02 = 19.61 g

Percent yield

Y = 16.67/19.61·100 = 84.99%

Answer

Y = 84.99%
3.Molarity & dilution

Answer: Vwater = 125 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 = 0.25·250/0.5 = 125 mL

Water to add

Vwater = 250 − 125 = 125 mL

Answer

Vwater = 125 mL
4.Molarity & dilution

Answer: c = 0.1857 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 = 0.2·300 + 0.1·50 = 65 mmol

Concentration of the mixture

c = 65/350 = 0.1857 mol/L

Answer

c = 0.1857 mol/L
5.Ideal gas law

Answer: P = 177 kPa

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

Moles

n = m/M = 40/28.01 = 1.428 mol
T = 25 + 273.15 = 298.1 K

Pressure

P = nRT/V = 1.428·8.314·298.1/0.02 = 177 kPa

Answer

P = 177 kPa
6.Ideal gas law

Answer: V2 = 6.773 L

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

Absolute temperatures

T1 = 283.1 K, T2 = 493.1 K

Combined gas law

V2 = V1·(P1/P2)·(T2/T1) = 5·(350/450)·(493.1/283.1) = 6.773 L

Answer

V2 = 6.773 L
7.Calorimetry & enthalpy

Answer: Tf = 29.81 °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

75·0.897·(120 − Tf) = 250·4.18·(Tf − 24)

Solve for the final temperature

Tf = (67.28·120 + 1045·24)/(67.28 + 1045) = 29.81 °C

Answer

Tf = 29.81 °C
8.Calorimetry & enthalpy

Answer: q = 5668 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) + 4·(−285.8)] − [2·(−238.7) + 3·0] = −1453 kJ

Heat for the given mass

n = 250/32.04 = 7.803 mol
q = n·|ΔH°/2| = 7.803·726.4 = 5668 kJ

Answer

q = 5668 kJ
9.Chemical equilibrium

Answer: [HI] = 0.6 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

36 = (2x)²/(0.4 − x)²

Take the square root

6 = 2x/(0.4 − x) → x = 0.4·6/(2 + 6) = 0.3 mol/L

Equilibrium concentration

[HI] = 2x = 0.6 mol/L

Answer

[HI] = 0.6 mol/L
10.Chemical equilibrium

Answer: [Cl2] = 0.2317 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/(0.5 − x) → x² + 0.2·x − 0.1 = 0

Solve the quadratic

x = (−0.2 + √(0.2² + 4·0.1))/2 = 0.2317 mol/L

Equilibrium concentration

[Cl₂] = x = 0.2317 mol/L

Answer

[Cl2] = 0.2317 mol/L
11.pH & buffers

Answer: pH = 2.253

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/(0.5 − x) → x = 0.005581 mol/L

pH

pH = −log(0.005581) = 2.253

Answer

pH = 2.253
12.pH & buffers

Answer: pH = 3.548

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 − 0.025 = 0.275 mol
n(A⁻) = 0.15 + 0.025 = 0.175 mol

Henderson–Hasselbalch

pH = 3.745 + log(0.175/0.275) = 3.548

Answer

pH = 3.548
13.Reaction kinetics

Answer: k = 0.008514 min⁻¹

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).

Integrated first-order law

k = ln(CA0/CA)/t = ln(1/0.6)/60 = 0.5108/60 = 0.008514 min⁻¹

Answer

k = 0.008514 min⁻¹
14.Reaction kinetics

Answer: Ea = 69.91 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 = 308.1 K, T2 = 333.1 K

Solve Arrhenius for Ea

Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·2.048/(-2.435e-4) = 69910 J/mol
Ea = 69.91 kJ/mol

Answer

Ea = 69.91 kJ/mol

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