12 g of H2 and 8 g of O2 react according to 2H2 + O2 → 2H2O. What mass m of H2O can form?
M(H2) = 2.016M(O2) = 32M(H2O) = 18.02 g/mol
m = g
2.StoichiometryHard
In the reaction 2Na + Cl2 → 2NaCl, 6 g of Na reacts completely (the other reactants are in excess) and 13.88 g of NaCl is collected. Find the percent yield Y.
M(Na) = 22.99 g/molM(NaCl) = 58.44 g/molactual: 13.88 g
Y = %
3.Molarity & dilutionMedium
You need 200 mL of 0.2 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 = 0.2 mol/LV2 = 200 mL
V1 = mL
4.Molarity & dilutionHard
50 mL of a 1 mol/L solution is mixed with 200 mL of a 0.05 mol/L solution of the same substance. Find the concentration c of the mixture (volumes are additive).
c1 = 1 mol/LV1 = 50 mLc2 = 0.05 mol/LV2 = 200 mL
c = mol/L
5.Ideal gas lawMedium
A tank of 30 L contains 230 g of O₂ at 55 °C. Treat it as an ideal gas and find the pressure P.
A 75 g block of copper (c = 0.385 J/(g·°C)) at 110 °C is dropped into 100 g of water (c = 4.18 J/(g·°C)) at 25 °C in an insulated cup. Find the final temperature Tf.
1 mol/L of H₂ and 1 mol/L of I₂ are put in a container and react: H₂ + I₂ ⇌ 2HI, with Kc = 16. Find the equilibrium concentration [H2].
[H₂]₀ = [I₂]₀ = 1 mol/LKc = 16
[H2] = mol/L
10.Chemical equilibriumHard
PCl₅ decomposes: PCl₅ ⇌ PCl₃ + Cl₂, with Kc = 0.02 at the reaction temperature. A container starts with 1.5 mol/L of PCl₅ only. Find the equilibrium concentration [Cl2].
[PCl₅]₀ = 1.5 mol/LKc = 0.02
[Cl2] = mol/L
11.pH & buffersMedium
Find the pH pH of a 0.01 mol/L solution of acetic acid (Ka = 1.8 × 10⁻⁵).
c = 0.01 mol/LKa = 1.8 × 10⁻⁵
pH =
12.pH & buffersHard
A buffer contains 0.2 mol/L acetic acid and 0.15 mol/L of its sodium salt. Ka = 1.8 × 10⁻⁵. Find the pH pH of the buffer.
[HA] = 0.2[A⁻] = 0.15Ka = 1.8 × 10⁻⁵
pH =
13.Reaction kineticsMedium
A second-order reaction (−rA = k·CA²) has k = 0.8 L/(mol·min) and an initial concentration of 0.2 mol/L. Find its first half-life t½.
k = 0.8 L/(mol·min)CA0 = 0.2 mol/L
t½ = min
14.Reaction kineticsHard
A first-order reaction has a rate constant of 0.05 s⁻¹ at 60 °C and an activation energy of 90 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(H2) = 12/2.016 = 5.952 mol
n(O2) = 8/32 = 0.25 mol
Limiting reactant
5.952/2 = 2.976, 0.25/1 = 0.25 → O2
Mass of product
n(H2O) = 0.25·2 = 0.5 mol
m = 0.5·18.02 = 9.01 g
Answer
m = 9.01 g
2.Stoichiometry
Answer: Y = 91.01 %
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(Na) = 6/22.99 = 0.261 mol
m = 0.261·2/2·58.44 = 15.25 g
Percent yield
Y = 13.88/15.25·100 = 91.01%
Answer
Y = 91.01%
3.Molarity & dilution
Answer: V1 = 16 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 = 0.2·200/2.5 = 16 mL
Answer
V1 = 16 mL
4.Molarity & dilution
Answer: c = 0.24 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 = 1·50 + 0.05·200 = 60 mmol
Concentration of the mixture
c = 60/250 = 0.24 mol/L
Answer
c = 0.24 mol/L
5.Ideal gas law
Answer: P = 653.6 kPa
Ideal gas law: PV = nRT, with n = m/M.
Moles
n = m/M = 230/32 = 7.188 mol
T = 55 + 273.15 = 328.1 K
Pressure
P = nRT/V = 7.188·8.314·328.1/0.03 = 653.6 kPa
Answer
P = 653.6 kPa
6.Ideal gas law
Answer: ρ = 0.3119 kg/m³
Ideal gas density: ρ = PM/(RT).
Rearrange the gas law
PV = (m/M)RT → ρ = m/V = PM/(RT)
T = 190 + 273.15 = 463.1 K
Density
ρ = 300·4.003/(8.314·463.1) = 0.3119 kg/m³
Answer
ρ = 0.3119 kg/m³
7.Calorimetry & enthalpy
Answer: Tf = 30.49 °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
75·0.385·(110 − Tf) = 100·4.18·(Tf − 25)
Solve for the final temperature
Tf = (28.88·110 + 418·25)/(28.88 + 418) = 30.49 °C
Answer
Tf = 30.49 °C
8.Calorimetry & enthalpy
Answer: ΔH° = −1367 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: [H2] = 0.3333 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
16 = (2x)²/(1 − x)²
Take the square root
4 = 2x/(1 − x) → x = 1·4/(2 + 4) = 0.6667 mol/L
Equilibrium concentration
[H₂] = 1 − x = 0.3333 mol/L
Answer
[H2] = 0.3333 mol/L
10.Chemical equilibrium
Answer: [Cl2] = 0.1635 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/(1.5 − x) → x² + 0.02·x − 0.03 = 0
Solve the quadratic
x = (−0.02 + √(0.02² + 4·0.03))/2 = 0.1635 mol/L
Equilibrium concentration
[Cl₂] = x = 0.1635 mol/L
Answer
[Cl2] = 0.1635 mol/L
11.pH & buffers
Answer: pH = 3.382
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/(0.01 − x) → x = 0.0004154 mol/L
pH
pH = −log(0.0004154) = 3.382
Answer
pH = 3.382
12.pH & buffers
Answer: pH = 4.62
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 = 4.745
Henderson–Hasselbalch
pH = 4.745 + log(0.15/0.2) = 4.62
Answer
pH = 4.62
13.Reaction kinetics
Answer: t½ = 6.25 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/(0.8·0.2) = 6.25 min
Answer
t½ = 6.25 min
Each later half-life is twice as long, because C₀ has halved.
14.Reaction kinetics
Answer: A = 6.465 × 10¹² 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).