30 g of Mg and 48 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
In the reaction N2 + 3H2 → 2NH3, 12 g of N2 reacts completely (the other reactants are in excess) and 10.94 g of NH3 is collected. Find the percent yield Y.
M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 10.94 g
Y = %
3.Molarity & dilutionMedium
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
300 mL of a 1.5 mol/L solution is mixed with 400 mL of a 0.3 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 75 g block of aluminium (c = 0.897 J/(g·°C)) at 160 °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.
0.25 mol/L of H₂ and 0.25 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [HI].
[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 9
[HI] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 0.2 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].
[PCl₅]₀ = 0.2 mol/LKc = 0.1
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.5 mol/L solution of hydrofluoric acid (Ka = 0.00068).
c = 0.5 mol/LKa = 0.00068
pH =
12.pH & buffersHard
A buffer contains 0.4 mol/L formic acid and 0.8 mol/L of its sodium salt. Ka = 0.00018. Find the pH pH of the buffer.
[HA] = 0.4[A⁻] = 0.8Ka = 0.00018
pH =
13.Reaction kineticsMedium
A second-order reaction (−rA = k·CA²) has k = 0.25 L/(mol·min) and an initial concentration of 0.5 mol/L. Find its first half-life t½.
k = 0.25 L/(mol·min)CA0 = 0.5 mol/L
t½ = min
14.Reaction kineticsHard
The rate constant of a reaction is 0.01 min⁻¹ at 35 °C and 0.0259 min⁻¹ at 55 °C. Find the activation energy Ea.
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) = 30/24.31 = 1.234 mol
n(O2) = 48/32 = 1.5 mol
Limiting reactant
1.234/2 = 0.617, 1.5/1 = 1.5 → Mg
Mass of product
n(MgO) = 0.617·2 = 1.234 mol
m = 1.234·40.3 = 49.73 g
Answer
m = 49.73 g
2.Stoichiometry
Answer: Y = 75 %
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(N2) = 12/28.02 = 0.4283 mol
m = 0.4283·2/1·17.03 = 14.59 g
Percent yield
Y = 10.94/14.59·100 = 75%
Answer
Y = 75%
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 = 0.8143 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 = 1.5·300 + 0.3·400 = 570 mmol
Concentration of the mixture
c = 570/700 = 0.8143 mol/L
Answer
c = 0.8143 mol/L
5.Ideal gas law
Answer: V = 6.523 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 20/16.04 = 1.247 mol
T = 10 + 273.15 = 283.1 K
Volume
V = nRT/P = 1.247·8.314·283.1/450 = 6.523 L
Answer
V = 6.523 L
6.Ideal gas law
Answer: ρ = 1.914 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 130 + 273.15 = 403.1 K
Density
ρ = 400·16.04/(8.314·403.1) = 1.914 kg/m³
Answer
ρ = 1.914 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 42.85 °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·(160 − Tf) = 100·4.18·(Tf − 24)
Solve for the final temperature
Tf = (67.28·160 + 418·24)/(67.28 + 418) = 42.85 °C
Answer
Tf = 42.85 °C
8.Calorimetry & enthalpy
Answer: ΔH° = −1453 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.
Negative: the reaction gives off heat (exothermic).
9.Chemical equilibrium
Answer: [HI] = 0.3 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.
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
0.1 = x²/(0.2 − x) → x² + 0.1·x − 0.02 = 0
Solve the quadratic
x = (−0.1 + √(0.1² + 4·0.02))/2 = 0.1 mol/L
Equilibrium concentration
[Cl₂] = x = 0.1 mol/L
Answer
[Cl2] = 0.1 mol/L
11.pH & buffers
Answer: pH = 1.742
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 = 0.0181 mol/L
pH
pH = −log(0.0181) = 1.742
Answer
pH = 1.742
12.pH & buffers
Answer: pH = 4.046
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]).
pKa
pKa = 3.745
Henderson–Hasselbalch
pH = 3.745 + log(0.8/0.4) = 4.046
Answer
pH = 4.046
13.Reaction kinetics
Answer: t½ = 8 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/(0.25·0.5) = 8 min
Answer
t½ = 8 min
Each later half-life is twice as long, because C₀ has halved.
14.Reaction kinetics
Answer: Ea = 40 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 = 328.1 K
Solve Arrhenius for Ea
Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·0.9517/(-1.978e-4) = 40003 J/mol