12 g of H2 and 40 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 N2 + 3H2 → 2NH3, 16 g of N2 reacts completely (the other reactants are in excess) and 12.06 g of NH3 is collected. Find the percent yield Y.
M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 12.06 g
Y = %
3.Molarity & dilutionMedium
You need 1000 mL of 0.5 mol/L solution and have a 5 mol/L stock solution. What volume V1 of stock solution do you need?
c1 = 5 mol/Lc2 = 0.5 mol/LV2 = 1000 mL
V1 = mL
4.Molarity & dilutionHard
300 mL of a 0.25 mol/L solution is mixed with 500 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 250 g block of copper (c = 0.385 J/(g·°C)) at 170 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 17 °C in an insulated cup. Find the final temperature Tf.
Use the standard enthalpies of formation to find the heat q released when 50 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.
0.5 mol/L of H₂ and 0.5 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 25. Find the equilibrium concentration [HI].
[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 25
[HI] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.04 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].
[PCl₅]₀ = 1.5 mol/LKc = 0.04
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.1 mol/L solution of lactic acid (Ka = 0.00014).
c = 0.1 mol/LKa = 0.00014
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.3 mol hydrofluoric acid and 0.25 mol of its conjugate base (Ka = 0.00068). 0.025 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(H2) = 12/2.016 = 5.952 mol
n(O2) = 40/32 = 1.25 mol
Limiting reactant
5.952/2 = 2.976, 1.25/1 = 1.25 → O2
Mass of product
n(H2O) = 1.25·2 = 2.5 mol
m = 2.5·18.02 = 45.05 g
Answer
m = 45.05 g
2.Stoichiometry
Answer: Y = 62.01 %
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) = 16/28.02 = 0.571 mol
m = 0.571·2/1·17.03 = 19.45 g
Percent yield
Y = 12.06/19.45·100 = 62.01%
Answer
Y = 62.01%
3.Molarity & dilution
Answer: V1 = 100 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 = 0.5·1000/5 = 100 mL
Answer
V1 = 100 mL
4.Molarity & dilution
Answer: c = 1.656 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 = 0.25·300 + 2.5·500 = 1325 mmol
Concentration of the mixture
c = 1325/800 = 1.656 mol/L
Answer
c = 1.656 mol/L
5.Ideal gas law
Answer: V = 37.65 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 140/16.04 = 8.728 mol
T = 90 + 273.15 = 363.1 K
Volume
V = nRT/P = 8.728·8.314·363.1/700 = 37.65 L
Answer
V = 37.65 L
6.Ideal gas law
Answer: ρ = 7.479 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 190 + 273.15 = 463.1 K
Density
ρ = 900·32/(8.314·463.1) = 7.479 kg/m³
Answer
ρ = 7.479 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 37.36 °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
250·0.385·(170 − Tf) = 150·4.18·(Tf − 17)
Solve for the final temperature
Tf = (96.25·170 + 627·17)/(96.25 + 627) = 37.36 °C
Answer
Tf = 37.36 °C
8.Calorimetry & enthalpy
Answer: q = 777.6 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
0.04 = x²/(1.5 − x) → x² + 0.04·x − 0.06 = 0
Solve the quadratic
x = (−0.04 + √(0.04² + 4·0.06))/2 = 0.2258 mol/L
Equilibrium concentration
[Cl₂] = x = 0.2258 mol/L
Answer
[Cl2] = 0.2258 mol/L
11.pH & buffers
Answer: pH = 2.435
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 = 0.003672 mol/L
pH
pH = −log(0.003672) = 2.435
Answer
pH = 2.435
12.pH & buffers
Answer: pH = 3.167
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⁻) = 0.25 + 0.025 = 0.275 mol
Henderson–Hasselbalch
pH = 3.167 + log(0.275/0.275) = 3.167
Answer
pH = 3.167
13.Reaction kinetics
Answer: t = 7.2 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).
Amount converted
CA0·X = 1.2·0.3 = 0.36 mol/L
Time
t = CA0·X/k = 0.36/0.05 = 7.2 min
Answer
t = 7.2 min
14.Reaction kinetics
Answer: Ea = 89.96 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 = 348.1 K
Solve Arrhenius for Ea
Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·4.034/(-3.728e-4) = 89958 J/mol