8 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 2Al + 3Cl2 → 2AlCl3, 4 g of Al reacts completely (the other reactants are in excess) and 17.4 g of AlCl3 is collected. Find the percent yield Y.
M(Al) = 26.98 g/molM(AlCl3) = 133.33 g/molactual: 17.4 g
Y = %
3.Molarity & dilutionMedium
You need 1000 mL of 0.2 mol/L solution and have a 0.5 mol/L stock solution. What volume V1 of stock solution do you need?
c1 = 0.5 mol/Lc2 = 0.2 mol/LV2 = 1000 mL
V1 = mL
4.Molarity & dilutionHard
150 mL of a 0.1 mol/L solution is mixed with 250 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 200 g block of iron (c = 0.449 J/(g·°C)) at 80 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 16 °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 [HI].
[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 54
[HI] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].
[PCl₅]₀ = 1.5 mol/LKc = 0.1
[PCl5] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.5 mol/L solution of formic acid (Ka = 0.00018).
c = 0.5 mol/LKa = 0.00018
pH =
12.pH & buffersHard
A buffer contains 0.4 mol/L formic acid and 0.1 mol/L of its sodium salt. Ka = 0.00018. Find the pH pH of the buffer.
[HA] = 0.4[A⁻] = 0.1Ka = 0.00018
pH =
13.Reaction kineticsMedium
In a first-order reaction the concentration of A falls from 0.8 mol/L to 0.28 mol/L in 30 min. Find the rate constant k.
CA0 = 0.8 mol/LCA = 0.28 mol/Lt = 30 min
k = min⁻¹
14.Reaction kineticsHard
The rate constant of a reaction is 0.005 min⁻¹ at 20 °C and 0.0719 min⁻¹ at 50 °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(H2) = 8/2.016 = 3.968 mol
n(O2) = 40/32 = 1.25 mol
Limiting reactant
3.968/2 = 1.984, 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 = 88.02 %
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(Al) = 4/26.98 = 0.1483 mol
m = 0.1483·2/2·133.33 = 19.77 g
Percent yield
Y = 17.4/19.77·100 = 88.02%
Answer
Y = 88.02%
3.Molarity & dilution
Answer: V1 = 400 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 = 0.2·1000/0.5 = 400 mL
Answer
V1 = 400 mL
4.Molarity & dilution
Answer: c = 1.6 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 = 0.1·150 + 2.5·250 = 640 mmol
Concentration of the mixture
c = 640/400 = 1.6 mol/L
Answer
c = 1.6 mol/L
5.Ideal gas law
Answer: P = 443.3 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 260/32 = 8.125 mol
T = 55 + 273.15 = 328.1 K
Pressure
P = nRT/V = 8.125·8.314·328.1/0.05 = 443.3 kPa
Answer
P = 443.3 kPa
6.Ideal gas law
Answer: V2 = 13.39 L
Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.
Absolute temperatures
T1 = 308.1 K, T2 = 383.1 K
Combined gas law
V2 = V1·(P1/P2)·(T2/T1) = 20·(350/650)·(383.1/308.1) = 13.39 L
Answer
V2 = 13.39 L
7.Calorimetry & enthalpy
Answer: Tf = 19.26 °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
200·0.449·(80 − Tf) = 400·4.18·(Tf − 16)
Solve for the final temperature
Tf = (89.8·80 + 1672·16)/(89.8 + 1672) = 19.26 °C
Answer
Tf = 19.26 °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] = 0.393 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/(1.5 − x) → x² + 0.1·x − 0.15 = 0
Solve the quadratic
x = (−0.1 + √(0.1² + 4·0.15))/2 = 0.3405 mol/L
Equilibrium concentration
[PCl₅] = 1.5 − 0.3405 = 1.159 mol/L
Answer
[PCl5] = 1.159 mol/L
11.pH & buffers
Answer: pH = 2.027
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 = 0.009397 mol/L
pH
pH = −log(0.009397) = 2.027
Answer
pH = 2.027
12.pH & buffers
Answer: pH = 3.143
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(0.1/0.4) = 3.143
Answer
pH = 3.143
13.Reaction kinetics
Answer: k = 0.03499 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(0.8/0.28)/30 = 1.05/30 = 0.03499 min⁻¹
Answer
k = 0.03499 min⁻¹
14.Reaction kinetics
Answer: Ea = 69.99 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 = 293.1 K, T2 = 323.1 K
Solve Arrhenius for Ea
Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·2.666/(-3.167e-4) = 69987 J/mol