In the reaction C6H12O6 → 2C2H5OH + 2CO2, 20 g of C6H12O6 reacts completely (the other reactants are in excess) and 9 g of C2H5OH is collected. Find the percent yield Y.
M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 9 g
Y = %
3.Molarity & dilutionMedium
You need 1000 mL of 0.2 mol/L solution and have a 2.5 mol/L stock solution. How much water Vwater do you add to the stock solution?
c1 = 2.5 mol/Lc2 = 0.2 mol/LV2 = 1000 mL
Vwater = mL
4.Molarity & dilutionHard
50 mL of a 0.25 mol/L solution is mixed with 400 mL of a 0.6 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 75 g block of copper (c = 0.385 J/(g·°C)) at 80 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 20 °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 = 54. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 54
[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 [Cl2].
[PCl₅]₀ = 0.8 mol/LKc = 0.2
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.25 mol/L solution of benzoic acid (Ka = 6.3 × 10⁻⁵).
c = 0.25 mol/LKa = 6.3 × 10⁻⁵
pH =
12.pH & buffersHard
A buffer contains 0.5 mol/L acetic acid and 0.15 mol/L of its sodium salt. Ka = 1.8 × 10⁻⁵. Find the pH pH of the buffer.
[HA] = 0.5[A⁻] = 0.15Ka = 1.8 × 10⁻⁵
pH =
13.Reaction kineticsMedium
A second-order reaction (−rA = k·CA²) has k = 0.8 L/(mol·min) and an initial concentration of 0.2 mol/L. Find its first half-life t½.
k = 0.8 L/(mol·min)CA0 = 0.2 mol/L
t½ = min
14.Reaction kineticsHard
A reaction has an activation energy of 80 kJ/mol. At 25 °C it is too slow. To what temperature T2 (in °C) must it be heated to make it 10 times faster?
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(Fe2O3) = 24/159.69 = 0.1503 mol
n(CO) = 64/28.01 = 2.285 mol
Limiting reactant
0.1503/1 = 0.1503, 2.285/3 = 0.7616 → Fe2O3
Mass of product
n(CO2) = 0.1503·3 = 0.4509 mol
m = 0.4509·44.01 = 19.84 g
Answer
m = 19.84 g
2.Stoichiometry
Answer: Y = 87.99 %
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(C6H12O6) = 20/180.16 = 0.111 mol
m = 0.111·2/1·46.07 = 10.23 g
Percent yield
Y = 9/10.23·100 = 87.99%
Answer
Y = 87.99%
3.Molarity & dilution
Answer: Vwater = 920 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 = 0.2·1000/2.5 = 80 mL
Water to add
Vwater = 1000 − 80 = 920 mL
Answer
Vwater = 920 mL
4.Molarity & dilution
Answer: c = 0.5611 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 = 0.25·50 + 0.6·400 = 252.5 mmol
Concentration of the mixture
c = 252.5/450 = 0.5611 mol/L
Answer
c = 0.5611 mol/L
5.Ideal gas law
Answer: V = 14.49 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 110/39.95 = 2.753 mol
T = 75 + 273.15 = 348.1 K
Volume
V = nRT/P = 2.753·8.314·348.1/550 = 14.49 L
Answer
V = 14.49 L
6.Ideal gas law
Answer: ρ = 13.59 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 10 + 273.15 = 283.1 K
Density
ρ = 1000·32/(8.314·283.1) = 13.59 kg/m³
Answer
ρ = 13.59 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 21.02 °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
75·0.385·(80 − Tf) = 400·4.18·(Tf − 20)
Solve for the final temperature
Tf = (28.88·80 + 1672·20)/(28.88 + 1672) = 21.02 °C
Answer
Tf = 21.02 °C
8.Calorimetry & enthalpy
Answer: ΔH° = −2220 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] = 0.05348 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
0.2 = 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
[Cl₂] = x = 0.3123 mol/L
Answer
[Cl2] = 0.3123 mol/L
11.pH & buffers
Answer: pH = 2.405
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/(0.25 − x) → x = 0.003937 mol/L
pH
pH = −log(0.003937) = 2.405
Answer
pH = 2.405
12.pH & buffers
Answer: pH = 4.222
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 = 4.745
Henderson–Hasselbalch
pH = 4.745 + log(0.15/0.5) = 4.222
Answer
pH = 4.222
13.Reaction kinetics
Answer: t½ = 6.25 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/(0.8·0.2) = 6.25 min
Answer
t½ = 6.25 min
Each later half-life is twice as long, because C₀ has halved.
14.Reaction kinetics
Answer: T2 = 47.91 °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).