20 g of Mg and 8 g of O2 react according to 2Mg + O2 → 2MgO. What mass m of MgO can form?
M(Mg) = 24.31M(O2) = 32M(MgO) = 40.3 g/mol
m = g
2.StoichiometryHard
In the reaction N2 + 3H2 → 2NH3, 20 g of N2 reacts completely (the other reactants are in excess) and 19.94 g of NH3 is collected. Find the percent yield Y.
M(N2) = 28.02 g/molM(NH3) = 17.03 g/molactual: 19.94 g
Y = %
3.Molarity & dilutionMedium
You need 250 mL of 0.5 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 = 0.5 mol/LV2 = 250 mL
Vwater = mL
4.Molarity & dilutionHard
100 mL of a 1.5 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 250 g block of iron (c = 0.449 J/(g·°C)) at 200 °C is dropped into 400 g of water (c = 4.18 J/(g·°C)) at 23 °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 = 4. Find the equilibrium concentration [HI].
[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 4
[HI] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.05 at the reaction temperature. A container starts with 0.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].
[PCl₅]₀ = 0.5 mol/LKc = 0.05
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.2 mol/L solution of acetic acid (Ka = 1.8 × 10⁻⁵).
c = 0.2 mol/LKa = 1.8 × 10⁻⁵
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.2 mol formic acid and 0.2 mol of its conjugate base (Ka = 0.00018). 0.025 mol of NaOH is added. Find the new pH pH.
A first-order reaction in a batch reactor has k = 0.1 min⁻¹. How long does it take to reach 95% conversion? Find t.
k = 0.1 min⁻¹X = 95 %
t = min
14.Reaction kineticsHard
Two experiments measure the initial rate of A → products. With CA0 = 0.5 mol/L the rate is 0.01 mol/(L·s); with CA0 = 2 mol/L it is 0.64 mol/(L·s). Find the reaction order n with respect to A.
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(Mg) = 20/24.31 = 0.8227 mol
n(O2) = 8/32 = 0.25 mol
Limiting reactant
0.8227/2 = 0.4114, 0.25/1 = 0.25 → O2
Mass of product
n(MgO) = 0.25·2 = 0.5 mol
m = 0.5·40.3 = 20.15 g
Answer
m = 20.15 g
2.Stoichiometry
Answer: Y = 82.02 %
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(N2) = 20/28.02 = 0.7138 mol
m = 0.7138·2/1·17.03 = 24.31 g
Percent yield
Y = 19.94/24.31·100 = 82.02%
Answer
Y = 82.02%
3.Molarity & dilution
Answer: Vwater = 166.7 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 = 0.5·250/1.5 = 83.33 mL
Water to add
Vwater = 250 − 83.33 = 166.7 mL
Answer
Vwater = 166.7 mL
4.Molarity & dilution
Answer: c = 0.5667 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 = 1.5·100 + 0.1·200 = 170 mmol
Concentration of the mixture
c = 170/300 = 0.5667 mol/L
Answer
c = 0.5667 mol/L
5.Ideal gas law
Answer: P = 3581 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 210/32 = 6.563 mol
T = 55 + 273.15 = 328.1 K
Pressure
P = nRT/V = 6.563·8.314·328.1/0.005 = 3581 kPa
Answer
P = 3581 kPa
6.Ideal gas law
Answer: V2 = 1.724 L
Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.
Absolute temperatures
T1 = 283.1 K, T2 = 423.1 K
Combined gas law
V2 = V1·(P1/P2)·(T2/T1) = 5·(150/650)·(423.1/283.1) = 1.724 L
Answer
V2 = 1.724 L
7.Calorimetry & enthalpy
Answer: Tf = 34.14 °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
250·0.449·(200 − Tf) = 400·4.18·(Tf − 23)
Solve for the final temperature
Tf = (112.3·200 + 1672·23)/(112.3 + 1672) = 34.14 °C
Answer
Tf = 34.14 °C
8.Calorimetry & enthalpy
Answer: ΔH° = −890.3 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] = 0.25 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/(0.5 − x) → x² + 0.05·x − 0.025 = 0
Solve the quadratic
x = (−0.05 + √(0.05² + 4·0.025))/2 = 0.1351 mol/L
Equilibrium concentration
[Cl₂] = x = 0.1351 mol/L
Answer
[Cl2] = 0.1351 mol/L
11.pH & buffers
Answer: pH = 2.724
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/(0.2 − x) → x = 0.001888 mol/L
pH
pH = −log(0.001888) = 2.724
Answer
pH = 2.724
12.pH & buffers
Answer: pH = 3.854
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 − 0.025 = 0.175 mol
n(A⁻) = 0.2 + 0.025 = 0.225 mol
Henderson–Hasselbalch
pH = 3.745 + log(0.225/0.175) = 3.854
Answer
pH = 3.854
13.Reaction kinetics
Answer: t = 29.96 min
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).
Conversion and concentration
C/C0 = 1 − X = 0.05
Solve for the time
t = −ln(1 − X)/k = −ln(0.05)/0.1 = 29.96 min
Answer
t = 29.96 min
14.Reaction kinetics
Answer: n = 3
Method of initial rates: for r = k·Cⁿ, comparing two runs that differ only in the starting concentration removes k: r₂/r₁ = (C₂/C₁)ⁿ. Doubling C doubles the rate for first order and quadruples it for second order.