20 g of C3H8 and 16 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?
M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 g/mol
m = g
2.StoichiometryHard
In the reaction CH4 + 2O2 → CO2 + 2H2O, 20 g of CH4 reacts completely (the other reactants are in excess) and 42.24 g of H2O is collected. Find the percent yield Y.
M(CH4) = 16.04 g/molM(H2O) = 18.02 g/molactual: 42.24 g
Y = %
3.Molarity & dilutionMedium
You need 500 mL of 0.5 mol/L solution and have a 5 mol/L stock solution. How much water Vwater do you add to the stock solution?
c1 = 5 mol/Lc2 = 0.5 mol/LV2 = 500 mL
Vwater = mL
4.Molarity & dilutionHard
250 mL of a 0.8 mol/L solution is mixed with 100 mL of a 0.1 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 100 g block of lead (c = 0.129 J/(g·°C)) at 100 °C is dropped into 200 g of water (c = 4.18 J/(g·°C)) at 15 °C in an insulated cup. Find the final temperature Tf.
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 = 50. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 0.8 mol/LKc = 50
[H2] = mol/L
10.Chemical equilibriumHard
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
Find the pH pH of a 0.01 mol/L solution of hydrofluoric acid (Ka = 0.00068).
c = 0.01 mol/LKa = 0.00068
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.2 mol formic acid and 0.25 mol of its conjugate base (Ka = 0.00018). 0.02 mol of NaOH is added. Find the new pH pH.
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(C3H8) = 20/44.1 = 0.4535 mol
n(O2) = 16/32 = 0.5 mol
Limiting reactant
0.4535/1 = 0.4535, 0.5/5 = 0.1 → O2
Mass of product
n(H2O) = 0.1·4 = 0.4 mol
m = 0.4·18.02 = 7.208 g
Answer
m = 7.208 g
2.Stoichiometry
Answer: Y = 94 %
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) = 20/16.04 = 1.247 mol
m = 1.247·2/1·18.02 = 44.94 g
Percent yield
Y = 42.24/44.94·100 = 94%
Answer
Y = 94%
3.Molarity & dilution
Answer: Vwater = 450 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 = 0.5·500/5 = 50 mL
Water to add
Vwater = 500 − 50 = 450 mL
Answer
Vwater = 450 mL
4.Molarity & dilution
Answer: c = 0.6 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 = 0.8·250 + 0.1·100 = 210 mmol
Concentration of the mixture
c = 210/350 = 0.6 mol/L
Answer
c = 0.6 mol/L
5.Ideal gas law
Answer: P = 1031 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 180/44.01 = 4.09 mol
T = 30 + 273.15 = 303.1 K
Pressure
P = nRT/V = 4.09·8.314·303.1/0.01 = 1031 kPa
Answer
P = 1031 kPa
6.Ideal gas law
Answer: ρ = 14.09 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 0 + 273.15 = 273.1 K
Density
ρ = 1000·32/(8.314·273.1) = 14.09 kg/m³
Answer
ρ = 14.09 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 16.29 °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
100·0.129·(100 − Tf) = 200·4.18·(Tf − 15)
Solve for the final temperature
Tf = (12.9·100 + 836·15)/(12.9 + 836) = 16.29 °C
Answer
Tf = 16.29 °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: [H2] = 0.1764 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
0.05 = 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 = 2.64
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 = 0.00229 mol/L
pH
pH = −log(0.00229) = 2.64
Answer
pH = 2.64
12.pH & buffers
Answer: pH = 3.921
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 − 0.02 = 0.18 mol
n(A⁻) = 0.25 + 0.02 = 0.27 mol
Henderson–Hasselbalch
pH = 3.745 + log(0.27/0.18) = 3.921
Answer
pH = 3.921
13.Reaction kinetics
Answer: k = 0.1022 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(1.5/0.9)/5 = 0.5108/5 = 0.1022 min⁻¹
Answer
k = 0.1022 min⁻¹
14.Reaction kinetics
Answer: k2 = 0.9522 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).