8 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 CH4 + 2O2 → CO2 + 2H2O, 30 g of CH4 reacts completely (the other reactants are in excess) and 72.44 g of CO2 is collected. Find the percent yield Y.
M(CH4) = 16.04 g/molM(CO2) = 44.01 g/molactual: 72.44 g
Y = %
3.Molarity & dilutionMedium
You need 500 mL of 0.25 mol/L solution and have a 2.5 mol/L stock solution. What volume V1 of stock solution do you need?
c1 = 2.5 mol/Lc2 = 0.25 mol/LV2 = 500 mL
V1 = mL
4.Molarity & dilutionHard
250 mL of a 1 mol/L solution is mixed with 100 mL of a 1.2 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
c1 = 1 mol/LV1 = 250 mLc2 = 1.2 mol/LV2 = 100 mL
c = mol/L
5.Ideal gas lawMedium
What volume V does 120 g of O₂ occupy at 100 kPa and 15 °C? Treat it as an ideal gas.
A 200 g block of iron (c = 0.449 J/(g·°C)) at 170 °C is dropped into 150 g of water (c = 4.18 J/(g·°C)) at 22 °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.
0.4 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 1 mol/L of PCl₅ only. Find the equilibrium concentration [PCl5].
[PCl₅]₀ = 1 mol/LKc = 0.02
[PCl5] = 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 0.3 mol formic acid and 0.1 mol of its conjugate base (Ka = 0.00018). 0.02 mol of NaOH is added. Find the new pH pH.
In a first-order reaction the concentration of A falls from 1.5 mol/L to 0.3 mol/L in 10 min. Find the rate constant k.
CA0 = 1.5 mol/LCA = 0.3 mol/Lt = 10 min
k = min⁻¹
14.Reaction kineticsHard
A first-order reaction has a rate constant of 0.1 s⁻¹ at 30 °C and an activation energy of 50 kJ/mol. Find the pre-exponential factor A in the Arrhenius equation.
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) = 8/24.31 = 0.3291 mol
n(O2) = 8/32 = 0.25 mol
Limiting reactant
0.3291/2 = 0.1645, 0.25/1 = 0.25 → Mg
Mass of product
n(MgO) = 0.1645·2 = 0.3291 mol
m = 0.3291·40.3 = 13.26 g
Answer
m = 13.26 g
2.Stoichiometry
Answer: Y = 88.01 %
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(CH4) = 30/16.04 = 1.87 mol
m = 1.87·1/1·44.01 = 82.31 g
Percent yield
Y = 72.44/82.31·100 = 88.01%
Answer
Y = 88.01%
3.Molarity & dilution
Answer: V1 = 50 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 = 0.25·500/2.5 = 50 mL
Answer
V1 = 50 mL
4.Molarity & dilution
Answer: c = 1.057 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 = 1·250 + 1.2·100 = 370 mmol
Concentration of the mixture
c = 370/350 = 1.057 mol/L
Answer
c = 1.057 mol/L
5.Ideal gas law
Answer: V = 89.84 L
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = 120/32 = 3.75 mol
T = 15 + 273.15 = 288.1 K
Volume
V = nRT/P = 3.75·8.314·288.1/100 = 89.84 L
Answer
V = 89.84 L
6.Ideal gas law
Answer: V2 = 3.77 L
Combined gas law: for a fixed amount of ideal gas, P1V1/T1 = P2V2/T2.
Absolute temperatures
T1 = 313.1 K, T2 = 413.1 K
Combined gas law
V2 = V1·(P1/P2)·(T2/T1) = 20·(100/700)·(413.1/313.1) = 3.77 L
Answer
V2 = 3.77 L
7.Calorimetry & enthalpy
Answer: Tf = 40.54 °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·(170 − Tf) = 150·4.18·(Tf − 22)
Solve for the final temperature
Tf = (89.8·170 + 627·22)/(89.8 + 627) = 40.54 °C
Answer
Tf = 40.54 °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.
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: [PCl5] = 0.8682 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/(1 − x) → x² + 0.02·x − 0.02 = 0
Solve the quadratic
x = (−0.02 + √(0.02² + 4·0.02))/2 = 0.1318 mol/L
Equilibrium concentration
[PCl₅] = 1 − 0.1318 = 0.8682 mol/L
Answer
[PCl5] = 0.8682 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 = 3.377
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) = 0.3 − 0.02 = 0.28 mol
n(A⁻) = 0.1 + 0.02 = 0.12 mol
Henderson–Hasselbalch
pH = 3.745 + log(0.12/0.28) = 3.377
Answer
pH = 3.377
13.Reaction kinetics
Answer: k = 0.1609 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(1.5/0.3)/10 = 1.609/10 = 0.1609 min⁻¹
Answer
k = 0.1609 min⁻¹
14.Reaction kinetics
Answer: A = 4.127 × 10⁷ s⁻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).