30 g of Mg and 48 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 2Mg + O2 → 2MgO, 30 g of Mg reacts completely (the other reactants are in excess) and 27.35 g of MgO is collected. Find the percent yield Y.
M(Mg) = 24.31 g/molM(MgO) = 40.3 g/molactual: 27.35 g
Y = %
3.Molarity & dilutionMedium
You need 250 mL of 0.4 mol/L solution and have a 1.5 mol/L stock solution. What volume V1 of stock solution do you need?
c1 = 1.5 mol/Lc2 = 0.4 mol/LV2 = 250 mL
V1 = mL
4.Molarity & dilutionHard
250 mL of a 0.25 mol/L solution is mixed with 400 mL of a 2.5 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
A 50 g block of lead (c = 0.129 J/(g·°C)) at 190 °C is dropped into 250 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 C3H8 (M = 44.1 g/mol) burns completely: C3H8 + 5O₂ → 3CO₂ + 4H₂O(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 = 49. Find the equilibrium concentration [HI].
[H₂]₀ = [I₂]₀ = 0.5 mol/LKc = 49
[HI] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.1 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 = 0.1
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.1 mol/L solution of hypochlorous acid (Ka = 3 × 10⁻⁸).
c = 0.1 mol/LKa = 3 × 10⁻⁸
pH =
12.pH & buffersHard
A buffer contains 0.4 mol/L hydrofluoric acid and 0.5 mol/L of its sodium salt. Ka = 0.00068. Find the pH pH of the buffer.
[HA] = 0.4[A⁻] = 0.5Ka = 0.00068
pH =
13.Reaction kineticsMedium
In a first-order reaction the concentration of A falls from 0.5 mol/L to 0.25 mol/L in 15 min. Find the rate constant k.
CA0 = 0.5 mol/LCA = 0.25 mol/Lt = 15 min
k = min⁻¹
14.Reaction kineticsHard
Two experiments measure the initial rate of A → products. With CA0 = 0.1 mol/L the rate is 0.01 mol/(L·s); with CA0 = 0.2 mol/L it is 0.02 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) = 30/24.31 = 1.234 mol
n(O2) = 48/32 = 1.5 mol
Limiting reactant
1.234/2 = 0.617, 1.5/1 = 1.5 → Mg
Mass of product
n(MgO) = 0.617·2 = 1.234 mol
m = 1.234·40.3 = 49.73 g
Answer
m = 49.73 g
2.Stoichiometry
Answer: Y = 54.99 %
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(Mg) = 30/24.31 = 1.234 mol
m = 1.234·2/2·40.3 = 49.73 g
Percent yield
Y = 27.35/49.73·100 = 54.99%
Answer
Y = 54.99%
3.Molarity & dilution
Answer: V1 = 66.67 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 = 0.4·250/1.5 = 66.67 mL
Answer
V1 = 66.67 mL
4.Molarity & dilution
Answer: c = 1.635 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 = 0.25·250 + 2.5·400 = 1063 mmol
Concentration of the mixture
c = 1063/650 = 1.635 mol/L
Answer
c = 1.635 mol/L
5.Ideal gas law
Answer: V = 230.5 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 470/32 = 14.69 mol
T = 10 + 273.15 = 283.1 K
Volume
V = nRT/P = 14.69·8.314·283.1/150 = 230.5 L
Answer
V = 230.5 L
6.Ideal gas law
Answer: V2 = 0.9298 L
Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.
Absolute temperatures
T1 = 313.1 K, T2 = 473.1 K
Combined gas law
V2 = V1·(P1/P2)·(T2/T1) = 2·(200/650)·(473.1/313.1) = 0.9298 L
Answer
V2 = 0.9298 L
7.Calorimetry & enthalpy
Answer: Tf = 18.06 °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
50·0.129·(190 − Tf) = 250·4.18·(Tf − 17)
Solve for the final temperature
Tf = (6.45·190 + 1045·17)/(6.45 + 1045) = 18.06 °C
Answer
Tf = 18.06 °C
8.Calorimetry & enthalpy
Answer: q = 2517 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
0.1 = x²/(0.8 − x) → x² + 0.1·x − 0.08 = 0
Solve the quadratic
x = (−0.1 + √(0.1² + 4·0.08))/2 = 0.2372 mol/L
Equilibrium concentration
[Cl₂] = x = 0.2372 mol/L
Answer
[Cl2] = 0.2372 mol/L
11.pH & buffers
Answer: pH = 4.262
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 = 5.476 × 10⁻⁵ mol/L
pH
pH = −log(5.476 × 10⁻⁵) = 4.262
Answer
pH = 4.262
12.pH & buffers
Answer: pH = 3.264
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 = 3.167
Henderson–Hasselbalch
pH = 3.167 + log(0.5/0.4) = 3.264
Answer
pH = 3.264
13.Reaction kinetics
Answer: k = 0.04621 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(0.5/0.25)/15 = 0.6931/15 = 0.04621 min⁻¹
Answer
k = 0.04621 min⁻¹
14.Reaction kinetics
Answer: n = 1
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.