16 g of H2 and 48 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
In the reaction C3H8 + 5O2 → 3CO2 + 4H2O, 12 g of C3H8 reacts completely (the other reactants are in excess) and 14.71 g of H2O is collected. Find the percent yield Y.
M(C3H8) = 44.1 g/molM(H2O) = 18.02 g/molactual: 14.71 g
Y = %
3.Molarity & dilutionMedium
You need 1000 mL of 0.05 mol/L solution and have a 1.5 mol/L stock solution. How much water Vwater do you add to the stock solution?
c1 = 1.5 mol/Lc2 = 0.05 mol/LV2 = 1000 mL
Vwater = mL
4.Molarity & dilutionHard
300 mL of a 0.5 mol/L solution is mixed with 200 mL of a 0.1 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 150 g block of aluminium (c = 0.897 J/(g·°C)) at 200 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 19 °C in an insulated cup. Find the final temperature Tf.
Use the standard enthalpies of formation to find the heat q released when 20 g of C4H10 (M = 58.12 g/mol) burns completely: 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l). Give q as a positive number.
0.1 mol/L of H₂ and 0.1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 0.1 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 at the reaction temperature. A container starts with 0.8 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].
[PCl₅]₀ = 0.8 mol/LKc = 0.2
[PCl5] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.1 mol/L solution of hypochlorous acid (Ka = 3 × 10⁻⁸).
c = 0.1 mol/LKa = 3 × 10⁻⁸
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.3 mol hydrofluoric acid and 0.1 mol of its conjugate base (Ka = 0.00068). 0.01 mol of NaOH is added. Find the new pH pH.
A second-order reaction (−rA = k·CA²) has k = 0.02 L/(mol·min) and an initial concentration of 1 mol/L. Find its first half-life t½.
k = 0.02 L/(mol·min)CA0 = 1 mol/L
t½ = min
14.Reaction kineticsHard
A first-order reaction has k = 0.01 min⁻¹ at 30 °C and an activation energy of 50 kJ/mol. The batch reactor is now run at 45 °C for 30 min. Find the conversion X reached.
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) = 16/2.016 = 7.937 mol
n(O2) = 48/32 = 1.5 mol
Limiting reactant
7.937/2 = 3.968, 1.5/1 = 1.5 → O2
Mass of product
n(H2O) = 1.5·2 = 3 mol
m = 3·18.02 = 54.06 g
Answer
m = 54.06 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(C3H8) = 12/44.1 = 0.2721 mol
m = 0.2721·4/1·18.02 = 19.61 g
Percent yield
Y = 14.71/19.61·100 = 75%
Answer
Y = 75%
3.Molarity & dilution
Answer: Vwater = 966.7 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 = 0.05·1000/1.5 = 33.33 mL
Water to add
Vwater = 1000 − 33.33 = 966.7 mL
Answer
Vwater = 966.7 mL
4.Molarity & dilution
Answer: c = 0.34 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 = 0.5·300 + 0.1·200 = 170 mmol
Concentration of the mixture
c = 170/500 = 0.34 mol/L
Answer
c = 0.34 mol/L
5.Ideal gas law
Answer: V = 156.1 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 410/32 = 12.81 mol
T = 20 + 273.15 = 293.1 K
Volume
V = nRT/P = 12.81·8.314·293.1/200 = 156.1 L
Answer
V = 156.1 L
6.Ideal gas law
Answer: ρ = 7.22 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 180 + 273.15 = 453.1 K
Density
ρ = 850·32/(8.314·453.1) = 7.22 kg/m³
Answer
ρ = 7.22 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 50.98 °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
150·0.897·(200 − Tf) = 150·4.18·(Tf − 19)
Solve for the final temperature
Tf = (134.6·200 + 627·19)/(134.6 + 627) = 50.98 °C
Answer
Tf = 50.98 °C
8.Calorimetry & enthalpy
Answer: q = 990.2 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.
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
0.2 = x²/(0.8 − x) → x² + 0.2·x − 0.16 = 0
Solve the quadratic
x = (−0.2 + √(0.2² + 4·0.16))/2 = 0.3123 mol/L
Equilibrium concentration
[PCl₅] = 0.8 − 0.3123 = 0.4877 mol/L
Answer
[PCl5] = 0.4877 mol/L
11.pH & buffers
Answer: pH = 4.262
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/(0.1 − x) → x = 5.476 × 10⁻⁵ mol/L
pH
pH = −log(5.476 × 10⁻⁵) = 4.262
Answer
pH = 4.262
12.pH & buffers
Answer: pH = 2.746
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 − 0.01 = 0.29 mol
n(A⁻) = 0.1 + 0.01 = 0.11 mol
Henderson–Hasselbalch
pH = 3.167 + log(0.11/0.29) = 2.746
Answer
pH = 2.746
13.Reaction kinetics
Answer: t½ = 50 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/(0.02·1) = 50 min
Answer
t½ = 50 min
Each later half-life is twice as long, because C₀ has halved.
14.Reaction kinetics
Answer: X = 53.44 %
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).