24 g of Al and 8 g of Cl2 react according to 2Al + 3Cl2 → 2AlCl3. What mass m of AlCl3 can form?
M(Al) = 26.98M(Cl2) = 70.9M(AlCl3) = 133.33 g/mol
m = g
2.StoichiometryHard
In the reaction C6H12O6 → 2C2H5OH + 2CO2, 30 g of C6H12O6 reacts completely (the other reactants are in excess) and 9.51 g of C2H5OH is collected. Find the percent yield Y.
M(C6H12O6) = 180.16 g/molM(C2H5OH) = 46.07 g/molactual: 9.51 g
Y = %
3.Molarity & dilutionMedium
You need 250 mL of 0.4 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 = 0.4 mol/LV2 = 250 mL
Vwater = mL
4.Molarity & dilutionHard
300 mL of a 0.25 mol/L solution is mixed with 100 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 lead (c = 0.129 J/(g·°C)) at 120 °C is dropped into 300 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 250 g of C6H12O6 (M = 180.16 g/mol) burns completely: C6H12O6 + 6O₂ → 6CO₂ + 6H₂O(l). Give q as a positive number.
0.4 mol/L of H₂ and 0.4 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 9. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 0.4 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 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 = 0.02
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.1 mol/L solution of acetic acid (Ka = 1.8 × 10⁻⁵).
c = 0.1 mol/LKa = 1.8 × 10⁻⁵
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.1 mol formic acid and 0.15 mol of its conjugate base (Ka = 0.00018). 0.02 mol of NaOH is added. Find the new pH pH.
A second-order reaction (−rA = k·CA²) in a batch reactor has k = 0.25 L/(mol·min) and starts at 2 mol/L. How long does it take to reach 80% conversion? Find t.
k = 0.25 L/(mol·min)CA0 = 2 mol/LX = 80 %
t = min
14.Reaction kineticsHard
The rate constant of a reaction is 0.02 min⁻¹ at 40 °C and 0.201 min⁻¹ at 60 °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(Al) = 24/26.98 = 0.8895 mol
n(Cl2) = 8/70.9 = 0.1128 mol
Limiting reactant
0.8895/2 = 0.4448, 0.1128/3 = 0.03761 → Cl2
Mass of product
n(AlCl3) = 0.03761·2 = 0.07522 mol
m = 0.07522·133.33 = 10.03 g
Answer
m = 10.03 g
2.Stoichiometry
Answer: Y = 61.98 %
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) = 30/180.16 = 0.1665 mol
m = 0.1665·2/1·46.07 = 15.34 g
Percent yield
Y = 9.51/15.34·100 = 61.98%
Answer
Y = 61.98%
3.Molarity & dilution
Answer: Vwater = 183.3 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
Water to add
Vwater = 250 − 66.67 = 183.3 mL
Answer
Vwater = 183.3 mL
4.Molarity & dilution
Answer: c = 0.8125 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 + 2.5·100 = 325 mmol
Concentration of the mixture
c = 325/400 = 0.8125 mol/L
Answer
c = 0.8125 mol/L
5.Ideal gas law
Answer: P = 445.8 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 270/28.01 = 9.639 mol
T = 5 + 273.15 = 278.1 K
Pressure
P = nRT/V = 9.639·8.314·278.1/0.05 = 445.8 kPa
Answer
P = 445.8 kPa
6.Ideal gas law
Answer: V2 = 4.819 L
Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.
Absolute temperatures
T1 = 298.1 K, T2 = 383.1 K
Combined gas law
V2 = V1·(P1/P2)·(T2/T1) = 10·(300/800)·(383.1/298.1) = 4.819 L
Answer
V2 = 4.819 L
7.Calorimetry & enthalpy
Answer: Tf = 19.58 °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
250·0.129·(120 − Tf) = 300·4.18·(Tf − 17)
Solve for the final temperature
Tf = (32.25·120 + 1254·17)/(32.25 + 1254) = 19.58 °C
Answer
Tf = 19.58 °C
8.Calorimetry & enthalpy
Answer: q = 3888 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.
Equilibrium expression
9 = (2x)²/(0.4 − x)²
Take the square root
3 = 2x/(0.4 − x) → x = 0.4·3/(2 + 3) = 0.24 mol/L
Equilibrium concentration
[H₂] = 0.4 − x = 0.16 mol/L
Answer
[H2] = 0.16 mol/L
10.Chemical equilibrium
Answer: [Cl2] = 0.0905 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.
Equilibrium expression
0.02 = x²/(0.5 − x) → x² + 0.02·x − 0.01 = 0
Solve the quadratic
x = (−0.02 + √(0.02² + 4·0.01))/2 = 0.0905 mol/L
Equilibrium concentration
[Cl₂] = x = 0.0905 mol/L
Answer
[Cl2] = 0.0905 mol/L
11.pH & buffers
Answer: pH = 2.875
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 = 0.001333 mol/L
pH
pH = −log(0.001333) = 2.875
Answer
pH = 2.875
12.pH & buffers
Answer: pH = 4.072
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) = 0.1 − 0.02 = 0.08 mol
n(A⁻) = 0.15 + 0.02 = 0.17 mol
Henderson–Hasselbalch
pH = 3.745 + log(0.17/0.08) = 4.072
Answer
pH = 4.072
13.Reaction kinetics
Answer: t = 8 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).
Concentration at the end
CA = 2·(1 − 0.8) = 0.4 mol/L
Integrated second-order law
t = (1/CA − 1/CA0)/k = (2.5 − 0.5)/0.25 = 8 min
Answer
t = 8 min
14.Reaction kinetics
Answer: Ea = 100.1 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 = 313.1 K, T2 = 333.1 K
Solve Arrhenius for Ea
Ea = −R·ln(k2/k1)/(1/T2 − 1/T1) = −8.314·2.308/(-1.917e-4) = 100075 J/mol