12 g of C3H8 and 64 g of O2 react according to C3H8 + 5O2 → 3CO2 + 4H2O. What mass m of H2O can form?
M(C3H8) = 44.1M(O2) = 32M(H2O) = 18.02 g/mol
m = g
2.StoichiometryHard
In the reaction C6H12O6 → 2C2H5OH + 2CO2, 6 g of C6H12O6 reacts completely (the other reactants are in excess) and 2.76 g of CO2 is collected. Find the percent yield Y.
M(C6H12O6) = 180.16 g/molM(CO2) = 44.01 g/molactual: 2.76 g
Y = %
3.Molarity & dilutionMedium
You need 500 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 = 500 mL
V1 = mL
4.Molarity & dilutionHard
200 mL of a 1 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).
c1 = 1 mol/LV1 = 200 mLc2 = 2.5 mol/LV2 = 100 mL
c = mol/L
5.Ideal gas lawMedium
A tank of 30 L contains 230 g of N₂ at 85 °C. Treat it as an ideal gas and find the pressure P.
A 100 g block of lead (c = 0.129 J/(g·°C)) at 150 °C is dropped into 300 g of water (c = 4.18 J/(g·°C)) at 23 °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 C4H10 (M = 58.12 g/mol) burns completely: 2C4H10 + 13O₂ → 8CO₂ + 10H₂O(l). Give q as a positive number.
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 = 9. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 0.25 mol/LKc = 9
[H2] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.2 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 = 0.2
[PCl5] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.2 mol/L solution of hydrofluoric acid (Ka = 0.00068).
c = 0.2 mol/LKa = 0.00068
pH =
12.pH & buffersHard
A 1.00 L buffer contains 0.2 mol formic acid and 0.25 mol of its conjugate base (Ka = 0.00018). 0.01 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(C3H8) = 12/44.1 = 0.2721 mol
n(O2) = 64/32 = 2 mol
Limiting reactant
0.2721/1 = 0.2721, 2/5 = 0.4 → C3H8
Mass of product
n(H2O) = 0.2721·4 = 1.088 mol
m = 1.088·18.02 = 19.61 g
Answer
m = 19.61 g
2.Stoichiometry
Answer: Y = 94.15 %
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) = 6/180.16 = 0.0333 mol
m = 0.0333·2/1·44.01 = 2.931 g
Percent yield
Y = 2.76/2.931·100 = 94.15%
Answer
Y = 94.15%
3.Molarity & dilution
Answer: V1 = 133.3 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 = 0.4·500/1.5 = 133.3 mL
Answer
V1 = 133.3 mL
4.Molarity & dilution
Answer: c = 1.5 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 = 1·200 + 2.5·100 = 450 mmol
Concentration of the mixture
c = 450/300 = 1.5 mol/L
Answer
c = 1.5 mol/L
5.Ideal gas law
Answer: P = 815 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 230/28.01 = 8.211 mol
T = 85 + 273.15 = 358.1 K
Pressure
P = nRT/V = 8.211·8.314·358.1/0.03 = 815 kPa
Answer
P = 815 kPa
6.Ideal gas law
Answer: V2 = 6.217 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) = 10·(300/600)·(383.1/308.1) = 6.217 L
Answer
V2 = 6.217 L
7.Calorimetry & enthalpy
Answer: Tf = 24.29 °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
100·0.129·(150 − Tf) = 300·4.18·(Tf − 23)
Solve for the final temperature
Tf = (12.9·150 + 1254·23)/(12.9 + 1254) = 24.29 °C
Answer
Tf = 24.29 °C
8.Calorimetry & enthalpy
Answer: q = 2475 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
0.2 = x²/(1.5 − x) → x² + 0.2·x − 0.3 = 0
Solve the quadratic
x = (−0.2 + √(0.2² + 4·0.3))/2 = 0.4568 mol/L
Equilibrium concentration
[PCl₅] = 1.5 − 0.4568 = 1.043 mol/L
Answer
[PCl5] = 1.043 mol/L
11.pH & buffers
Answer: pH = 1.946
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 = 0.01133 mol/L
pH
pH = −log(0.01133) = 1.946
Answer
pH = 1.946
12.pH & buffers
Answer: pH = 3.881
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 − 0.01 = 0.19 mol
n(A⁻) = 0.25 + 0.01 = 0.26 mol
Henderson–Hasselbalch
pH = 3.745 + log(0.26/0.19) = 3.881
Answer
pH = 3.881
13.Reaction kinetics
Answer: t½ = 33.33 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).
Second-order half-life
t½ = 1/(k·CA0) = 1/(0.02·1.5) = 33.33 min
Answer
t½ = 33.33 min
Each later half-life is twice as long, because C₀ has halved.
14.Reaction kinetics
Answer: k2 = 0.083 min⁻¹
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).