The Mole Concept Definition The mole is the SI unit for amount of substance. One mole contains exactly 6.022 × 10 23 6.022 \times 10^{23} 6.022 × 1 0 23 elementary entities (atoms, molecules, ions, etc.).
Avogadro”s Constant N A = 6.022 × 10 23 m o l − 1 N_A = 6.022 \times 10^{23}\mathrm{ mol}^{-1} N A = 6.022 × 1 0 23 mol − 1 The number of particles N N N in n n n moles:
N = n × N A N = n \times N_A N = n × N A Molar Mass The molar mass M M M is the mass of one mole of a substance, expressed in g / m o l \mathrm{g/mol} g/mol .
N = m M N = \frac{m}{M} N = M m Where m m m is the mass in grams.
Substance Molar Mass (g/mol) H 1.01 C 12.01 N 14.01 O 16.00 Na 22.99 Cl 35.45 H2 _2 2 O 18.02 CO2 _2 2 44.01 NaCl 58.44 H2 _2 2 SO4 _4 4 98.08
Example
Calculate the number of molecules in 5.0 g 5.0\mathrm{ g} 5.0 g of water.
N = m M = 5.0 18.02 = 0.278 m o l N = \frac{m}{M} = \frac{5.0}{18.02} = 0.278\mathrm{ mol} N = M m = 18.02 5.0 = 0.278 mol N = 0.278 × 6.022 × 10 23 = 1.67 × 10 23 m o l e c u l e s N = 0.278 \times 6.022 \times 10^{23} = 1.67 \times 10^{23}\mathrm{ molecules} N = 0.278 × 6.022 × 1 0 23 = 1.67 × 1 0 23 molecules The empirical formula gives the simplest whole-number ratio of atoms in a compound.
The molecular formula gives the actual number of atoms of each element in a molecule.
M o l e c u l a r f o r m u l a = ( E m p i r i c a l f o r m u l a ) n \mathrm{Molecular formula} = (\mathrm{Empirical formula})_n Molecularformula = ( Empiricalformula ) n Where n n n is an integer.
Find the mass (or percentage) of each element. Convert masses to moles: n = m M n = \dfrac{m}{M} n = M m . Divide all mole values by the smallest mole value. Round to the nearest whole number (or multiply to get integers). Write the empirical formula. Example
A compound contains 40.0 % 40.0\% 40.0% carbon, 6.7 % 6.7\% 6.7% hydrogen, and 53.3 % 53.3\% 53.3% oxygen by mass. Find its Empirical formula.
Element Mass (g) Molar Mass (g/mol) Moles Ratio C 40.0 12.01 3.33 1 H 6.7 1.01 6.63 2 O 53.3 16.00 3.33 1
Empirical formula: CH2 _2 2 O.
If the molar mass is 180 g / m o l 180\mathrm{ g/mol} 180 g/mol The molecular formula is:
N = 180 30.03 = 6 N = \frac{180}{30.03} = 6 N = 30.03 180 = 6 Molecular formula: C6 _6 6 H12 _{12} 12 O6 _6 6 (glucose).
Hydrated Salts A hydrated salt contains water of crystallisation. The formula is written as, for example, CuSO4 _4 4 , ⋅ \cdot ⋅ 5H_ 2 \_2 _2 O.
To find the number of water molecules:
Heat the hydrated salt to remove water. Measure the mass loss. Calculate moles of anhydrous salt and moles of water. Find the ratio. Example
12.5 g 12.5\mathrm{ g} 12.5 g of hydrated copper(II) sulfate, CuSO4 _4 4 , ⋅ \cdot ⋅ xH2 _2 2 O, is heated to give 8.0 g 8.0\mathrm{ g} 8.0 g of anhydrous CuSO4 _4 4 . Find x x x .
Mass of water lost = 12.5 − 8.0 = 4.5 g = 12.5 - 8.0 = 4.5\mathrm{ g} = 12.5 − 8.0 = 4.5 g .
N ( C u S O 4 ) = 8.0 159.61 = 0.0501 m o l N(\mathrm{CuSO}_4) = \frac{8.0}{159.61} = 0.0501\mathrm{ mol} N ( CuSO 4 ) = 159.61 8.0 = 0.0501 mol N ( H 2 O ) = 4.5 18.02 = 0.250 m o l N(\mathrm{H}_2\mathrm{O}) = \frac{4.5}{18.02} = 0.250\mathrm{ mol} N ( H 2 O ) = 18.02 4.5 = 0.250 mol X = 0.250 0.0501 = 4.99 ≈ 5 X = \frac{0.250}{0.0501} = 4.99 \approx 5 X = 0.0501 0.250 = 4.99 ≈ 5 Formula: CuSO4 _4 4 , ⋅ \cdot ⋅ 5H_ 2 \_2 _2 O.
Chemical Equations and Balancing Balancing Equations Chemical equations must be balanced: the number of atoms of each element must be the same on both Sides (conservation of mass).
Steps Write the unbalanced equation with correct formulas. Count atoms of each element on both sides. Balance one element at a time using coefficients. Leave hydrogen and oxygen until last. Check that all elements are balanced. Ensure coefficients are in the lowest whole-number ratio. Example
Balance the combustion of propane:
Unbalanced: C3 _3 3 H8 _8 8 + O2 _2 2 → \to → CO2 _2 2 + H2 _2 2 O
Balance C: C3 _3 3 H8 _8 8 + O2 _2 2 → \to → 3CO2 _2 2 + H2 _2 2 O
Balance H: C3 _3 3 H8 _8 8 + O2 _2 2 → \to → 3CO2 _2 2 + 4H2 _2 2 O
Balance O: C3 _3 3 H8 _8 8 + 5O2 _2 2 → \to → 3CO2 _2 2 + 4H2 _2 2 O
Check: 3C, 8H, 10O on each side. Balanced.
Ionic Equations Spectator ions (ions that appear unchanged on both sides) can be removed to give a net ionic Equation .
Example
AgNO3 _3 3 (aq) + NaCl(aq) → \to → AgCl(s) + NaNO3 _3 3 (aq)
Full ionic: Ag+ ^+ + (aq) + NO3 − _3^- 3 − + Na+ ^+ + + Cl− ^- − → \to → AgCl(s) + Na+ ^+ + + NO3 − _3^- 3 −
Net ionic: Ag+ ^+ + (aq) + Cl− ^- − → \to → AgCl(s)
Reactant Calculations Limiting Reagent The limiting reagent is the reactant that is completely consumed first and therefore determines The maximum amount of product formed.
Steps Calculate moles of each reactant. Determine which reactant is limiting (divide moles by stoichiometric coefficient). Use the limiting reagent to calculate the amount of product. Example
5.0 g 5.0\mathrm{ g} 5.0 g of iron reacts with 3.0 g 3.0\mathrm{ g} 3.0 g of sulfur: Fe + S → \to → FeS.
N ( F e ) = 5.0 55.85 = 0.0895 m o l N(\mathrm{Fe}) = \frac{5.0}{55.85} = 0.0895\mathrm{ mol} N ( Fe ) = 55.85 5.0 = 0.0895 mol N ( S ) = 3.0 32.07 = 0.0936 m o l N(\mathrm{S}) = \frac{3.0}{32.07} = 0.0936\mathrm{ mol} N ( S ) = 32.07 3.0 = 0.0936 mol Stoichiometric ratio is 1:1, so Fe is the limiting reagent (fewer moles).
N ( F e S ) = 0.0895 m o l N(\mathrm{FeS}) = 0.0895\mathrm{ mol} N ( FeS ) = 0.0895 mol M ( F e S ) = 0.0895 × 87.91 = 7.87 g M(\mathrm{FeS}) = 0.0895 \times 87.91 = 7.87\mathrm{ g} M ( FeS ) = 0.0895 × 87.91 = 7.87 g Percentage Yield P e r c e n t a g e y i e l d = a c t u a l y i e l d t h e o r e t i c a l y i e l d × 100 % \mathrm{Percentage yield} = \frac{\mathrm{actual yield}}{\mathrm{theoretical yield}} \times 100\% Percentageyield = theoreticalyield actualyield × 100% Example
If 6.5 g 6.5\mathrm{ g} 6.5 g of FeS was actually produced in the previous example:
P e r c e n t a g e y i e l d = 6.5 7.87 × 100 % = 82.6 % \mathrm{Percentage yield} = \frac{6.5}{7.87} \times 100\% = 82.6\% Percentageyield = 7.87 6.5 × 100% = 82.6% Gas Laws Boyle’s Law (Constant Temperature) For a fixed amount of gas at constant temperature:
P 1 V 1 = P 2 V 2 P_1 V_1 = P_2 V_2 P 1 V 1 = P 2 V 2 Pressure is inversely proportional to volume: P ∝ 1 V P \propto \dfrac{1}{V} P ∝ V 1 .
Charles’s Law (Constant Pressure) For a fixed amount of gas at constant pressure:
V 1 T 1 = V 2 T 2 \frac{V_1}{T_1} = \frac{V_2}{T_2} T 1 V 1 = T 2 V 2 (Temperature must be in Kelvin.)
Volume is directly proportional to absolute temperature: V ∝ T V \propto T V ∝ T .
Gay-Lussac’s Law (Constant Volume) For a fixed amount of gas at constant volume:
P 1 T 1 = P 2 T 2 \frac{P_1}{T_1} = \frac{P_2}{T_2} T 1 P 1 = T 2 P 2 Pressure is directly proportional to absolute temperature: P ∝ T P \propto T P ∝ T .
The Ideal Gas Equation Combining all three laws:
P V = n R T PV = nRT P V = n R T Where:
P P P = pressure (Pa)V V V = volume (m3 ^3 3 )n n n = number of molesR R R = universal gas constant = 8.314 J / ( m o l ⋅ K ) = 8.314\mathrm{ J/(mol}\cdot\mathrm{K)} = 8.314 J/ ( mol ⋅ K ) T T T = temperature (K)Molar Volume At STP (0 ° C 0\degree\mathrm{C} 0° C , 100 k P a 100\mathrm{ kPa} 100 kPa ), one mole of any ideal gas occupies 22.7 L 22.7\mathrm{ L} 22.7 L .
At RTP (25 ° C 25\degree\mathrm{C} 25° C , 100 k P a 100\mathrm{ kPa} 100 kPa ), one mole occupies 24.8 L 24.8\mathrm{ L} 24.8 L .
Example
Calculate the volume occupied by 2.5 m o l 2.5\mathrm{ mol} 2.5 mol of gas at 25 ° C 25\degree\mathrm{C} 25° C and 1.2 a t m 1.2\mathrm{ atm} 1.2 atm .
P = 1.2 × 101325 = 121590 P a P = 1.2 \times 101325 = 121590\mathrm{ Pa} P = 1.2 × 101325 = 121590 Pa T = 298 K T = 298\mathrm{ K} T = 298 K V = \frac`\{nRT}`{P} = \frac{2.5 \times 8.314 \times 298}{121590} = \frac{6194.2}{121590} = 0.0509\mathrm{ m}^3 = 50.9\mathrm{ L} Real Gas Deviations Real gases deviate from ideal behaviour at:
High pressures (molecules are closer, intermolecular forces become significant).Low temperatures (molecules move slower, intermolecular forces become significant).Van der Waals Equation A more accurate equation for real gases:
( P + a n 2 V 2 ) ( V − n b ) = n R T \left(P + \frac{a n^2}{V^2}\right)\!\left(V - nb\right) = nRT ( P + V 2 a n 2 ) ( V − nb ) = n R T Where a a a accounts for intermolecular attractions and b b b accounts for molecular volume.
Kinetic Molecular Theory Assumptions Gas particles have negligible volume. Gas particles exert no forces on each other. All collisions are perfectly elastic. The average kinetic energy is proportional to temperature: E ˉ k = 3 2 k B T \bar{E}_k = \dfrac{3}{2}k_BT E ˉ k = 2 3 k B T . Solution Chemistry Concentration Molarity C = n V C = \frac{n}{V} C = V n Where c c c is in m o l / L \mathrm{mol/L} mol/L (or M), n n n in mol, and V V V in L.
Molality B = n s o l u t e m s o l v e n t B = \frac{n_{\mathrm{solute}}}{m_{\mathrm{solvent}}} B = m solvent n solute Where b b b is in m o l / k g \mathrm{mol/kg} mol/kg .
Mass Percentage % = m s o l u t e m s o l u t i o n × 100 % \% = \frac{m_{\mathrm{solute}}}{m_{\mathrm{solution}}} \times 100\% % = m solution m solute × 100% Parts Per Million (ppm) p p m = m s o l u t e m s o l u t i o n × 10 6 \mathrm{ppm} = \frac{m_{\mathrm{solute}}}{m_{\mathrm{solution}}} \times 10^6 ppm = m solution m solute × 1 0 6 Example
What is the concentration of a solution made by dissolving 10.0 g 10.0\mathrm{ g} 10.0 g of NaCl in enough water To make 250 m L 250\mathrm{ mL} 250 mL of solution?
N = 10.0 58.44 = 0.171 m o l N = \frac{10.0}{58.44} = 0.171\mathrm{ mol} N = 58.44 10.0 = 0.171 mol C = 0.171 0.250 = 0.684 m o l / L C = \frac{0.171}{0.250} = 0.684\mathrm{ mol/L} C = 0.250 0.171 = 0.684 mol/L Dilution C 1 V 1 = c 2 V 2 C_1 V_1 = c_2 V_2 C 1 V 1 = c 2 V 2 Example
What volume of 6.0 M 6.0\mathrm{ M} 6.0 M HCl is needed to make 500 m L 500\mathrm{ mL} 500 mL of 0.50 M 0.50\mathrm{ M} 0.50 M HCl?
V 1 = c 2 V 2 c 1 = 0.50 × 500 6.0 = 41.7 m L V_1 = \frac{c_2 V_2}{c_1} = \frac{0.50 \times 500}{6.0} = 41.7\mathrm{ mL} V 1 = c 1 c 2 V 2 = 6.0 0.50 × 500 = 41.7 mL Standard Solutions A standard solution is one of accurately known concentration. To prepare:
Calculate the mass of solute needed. Accurately weigh the solute. Dissolve in a small amount of solvent. Transfer to a volumetric flask. Add solvent to the calibration mark. Titration Calculations Titration is used to determine the concentration of an unknown solution by reacting it with a Standard solution.
Example
25.0 m L 25.0\mathrm{ mL} 25.0 mL of NaOH is titrated with 0.100 M 0.100\mathrm{ M} 0.100 M HCl. The endpoint is reached at 20.0 m L 20.0\mathrm{ mL} 20.0 mL of HCl. Find the concentration of NaOH.
N a O H + H C l → N a C l + H 2 O \mathrm{NaOH} + \mathrm{HCl} \to \mathrm{NaCl} + \mathrm{H}_2\mathrm{O} NaOH + HCl → NaCl + H 2 O N ( H C l ) = 0.100 × 0.0200 = 0.00200 m o l N(\mathrm{HCl}) = 0.100 \times 0.0200 = 0.00200\mathrm{ mol} N ( HCl ) = 0.100 × 0.0200 = 0.00200 mol Stoichiometry 1:1, so n ( N a O H ) = 0.00200 m o l n(\mathrm{NaOH}) = 0.00200\mathrm{ mol} n ( NaOH ) = 0.00200 mol .
C ( N a O H ) = 0.00200 0.0250 = 0.0800 M C(\mathrm{NaOH}) = \frac{0.00200}{0.0250} = 0.0800\mathrm{ M} C ( NaOH ) = 0.0250 0.00200 = 0.0800 M IB Exam-Style Questions Question 1 (Paper 1 style) What is the empirical formula of a compound that is 36.5 % 36.5\% 36.5% sodium, 25.4 % 25.4\% 25.4% sulfur, and 38.1 % 38.1\% 38.1% Oxygen?
Element Mass (g) Molar Mass Moles Ratio Na 36.5 22.99 1.588 2 S 25.4 32.07 0.792 1 O 38.1 16.00 2.381 3
Empirical formula: Na2 _2 2 SO3 _3 3 .
Question 2 (Paper 2 style) 10.0 g 10.0\mathrm{ g} 10.0 g of calcium carbonate (CaCO3 _3 3 ) is heated until completely decomposed: CaCO3 _3 3 → \to → CaO + CO2 _2 2 .
(a) Calculate the volume of CO2 _2 2 produced at RTP.
N ( C a C O 3 ) = 10.0 100.09 = 0.0999 m o l N(\mathrm{CaCO}_3) = \frac{10.0}{100.09} = 0.0999\mathrm{ mol} N ( CaCO 3 ) = 100.09 10.0 = 0.0999 mol N ( C O 2 ) = 0.0999 m o l N(\mathrm{CO}_2) = 0.0999\mathrm{ mol} N ( CO 2 ) = 0.0999 mol V = n × 24.8 = 0.0999 × 24.8 = 2.48 L V = n \times 24.8 = 0.0999 \times 24.8 = 2.48\mathrm{ L} V = n × 24.8 = 0.0999 × 24.8 = 2.48 L (b) Calculate the mass of CaO produced.
M ( C a O ) = 0.0999 × 56.08 = 5.60 g M(\mathrm{CaO}) = 0.0999 \times 56.08 = 5.60\mathrm{ g} M ( CaO ) = 0.0999 × 56.08 = 5.60 g Question 3 (Paper 1 style) A gas at 300 K 300\mathrm{ K} 300 K and 1.5 a t m 1.5\mathrm{ atm} 1.5 atm occupies 4.0 L 4.0\mathrm{ L} 4.0 L . What volume does it Occupy at 350 K 350\mathrm{ K} 350 K and 2.0 a t m 2.0\mathrm{ atm} 2.0 atm ?
P 1 V 1 T 1 = P 2 V 2 T 2 \frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2} T 1 P 1 V 1 = T 2 P 2 V 2 V 2 = P 1 V 1 T 2 P 2 T 1 = 1.5 × 4.0 × 350 2.0 × 300 = 2100 600 = 3.5 L V_2 = \frac{P_1 V_1 T_2}{P_2 T_1} = \frac{1.5 \times 4.0 \times 350}{2.0 \times 300} = \frac{2100}{600} = 3.5\mathrm{ L} V 2 = P 2 T 1 P 1 V 1 T 2 = 2.0 × 300 1.5 × 4.0 × 350 = 600 2100 = 3.5 L Question 4 (Paper 2 style) 3.0 g 3.0\mathrm{ g} 3.0 g of magnesium reacts with excess hydrochloric acid: Mg + 2HCl → \to → MgCl2 _2 2 + H2 _2 2 .
(a) Calculate the moles of hydrogen gas produced.
N ( M g ) = 3.0 24.31 = 0.123 m o l N(\mathrm{Mg}) = \frac{3.0}{24.31} = 0.123\mathrm{ mol} N ( Mg ) = 24.31 3.0 = 0.123 mol N ( H 2 ) = 0.123 m o l ( 1 : 1 r a t i o ) N(\mathrm{H}_2) = 0.123\mathrm{ mol} \mathrm{ (1:1 ratio)} N ( H 2 ) = 0.123 mol ( 1 : 1ratio ) (b) Calculate the volume of H2 _2 2 at STP.
V = 0.123 × 22.7 = 2.79 L V = 0.123 \times 22.7 = 2.79\mathrm{ L} V = 0.123 × 22.7 = 2.79 L (c) If only 2.5 L 2.5\mathrm{ L} 2.5 L of H2 _2 2 was collected, calculate the percentage yield.
P e r c e n t a g e y i e l d = 2.5 2.79 × 100 % = 89.6 % \mathrm{Percentage yield} = \frac{2.5}{2.79} \times 100\% = 89.6\% Percentageyield = 2.79 2.5 × 100% = 89.6% Summary Formula Expression Moles from mass n = m M n = \dfrac{m}{M} n = M m Particles N = n N A N = nN_A N = n N A Molarity c = n V c = \dfrac{n}{V} c = V n Ideal gas P V = n R T PV = nRT P V = n R T Boyle’s law P 1 V 1 = P 2 V 2 P_1V_1 = P_2V_2 P 1 V 1 = P 2 V 2 Charles’s law V 1 T 1 = V 2 T 2 \dfrac{V_1}{T_1} = \dfrac{V_2}{T_2} T 1 V 1 = T 2 V 2 Dilution c 1 V 1 = c 2 V 2 c_1V_1 = c_2V_2 c 1 V 1 = c 2 V 2 Percentage yield a c t u a l t h e o r e t i c a l × 100 % \dfrac{\mathrm{actual}}{\mathrm{theoretical}} \times 100\% theoretical actual × 100%
Exam Strategy
Always show your working with units. For gas calculations, ensure temperature is in Kelvin. For Titration calculations, identify the mole ratio from the balanced equation. Remember that Molar volume at STP is 22.7 L/mol and at RTP is 24.8 L/mol.
Gas Laws: Extended Dalton’s Law of Partial Pressures For a mixture of non-reacting gases:
P t o t a l = P 1 + P 2 + P 3 + ⋯ P_{\mathrm{total}} = P_1 + P_2 + P_3 + \cdots P total = P 1 + P 2 + P 3 + ⋯ The partial pressure of each gas:
P i = x i × P t o t a l P_i = x_i \times P_{\mathrm{total}} P i = x i × P total Where x i x_i x i is the mole fraction of gas i i i .
Graham’s Law of Diffusion The rate of diffusion (or effusion) of a gas is inversely proportional to the square root of its Molar mass:
r 1 r 2 = M 2 M 1 \frac{r_1}{r_2} = \sqrt{\frac{M_2}{M_1}} r 2 r 1 = M 1 M 2 Example
Compare the rates of diffusion of He (4 g/mol) and O2 _2 2 (32 g/mol).
r H e r O 2 = 32 4 = 8 = 2.83 \frac{r_{\mathrm{He}}}{r_{\mathrm{O}_2}} = \sqrt{\frac{32}{4}} = \sqrt{8} = 2.83 r O 2 r He = 4 32 = 8 = 2.83 Helium diffuses about 2.83 times faster than oxygen.
Ideal Gas Law Applications Molar Mass of a Gas M = \frac`\{mRT}``\{PV}` Density of a Gas \rho = \frac`\{PM}``\{RT}` Example
A gas has a density of 1.43 g / L 1.43\mathrm{ g/L} 1.43 g/L at STP. Find its molar mass.
M = ρ R T P = 1.43 × 8.314 × 273 101325 = 3247 101325 = 0.0320 k g / m o l = 32.0 g / m o l M = \frac{\rho RT}{P} = \frac{1.43 \times 8.314 \times 273}{101325} = \frac{3247}{101325} = 0.0320\mathrm{ kg/mol} = 32.0\mathrm{ g/mol} M = P ρR T = 101325 1.43 × 8.314 × 273 = 101325 3247 = 0.0320 kg/mol = 32.0 g/mol The gas is likely O2 _2 2 .
Solutions: Extended Concentration Conversions From To Method Molarity Mass percentage c × M × 100 / ( 1000 ρ ) c \times M \times 100 / (1000\rho) c × M × 100/ ( 1000 ρ ) Mass percentage Molarity ( % / 100 ) × ρ × 1000 / M (\%\mathrm{/}100) \times \rho \times 1000 / M ( % / 100 ) × ρ × 1000/ M Molarity ppm c × M × 10 6 / 1000 ρ c \times M \times 10^6 / 1000\rho c × M × 1 0 6 /1000 ρ
Colligative Properties Properties that depend on the number of solute particles (not their identity):
Boiling point elevation : Δ T b = i K b × m \Delta T_b = iK_b \times m Δ T b = i K b × m Freezing point depression : Δ T f = i K f × m \Delta T_f = iK_f \times m Δ T f = i K f × m Osmotic pressure : Π = i c R T \Pi = icRT Π = i c R T Where i i i is the van’t Hoff factor (number of particles per formula unit), K b K_b K b and K f K_f K f are Constants, and m m m is molality.
Solute i i i Non-electrolyte (e.g., glucose) 1 NaCl 2 CaCl2 _2 2 3
Water of Crystallisation: Extended Procedure :
Weigh the hydrated salt. Heat gently to drive off water. Cool in a desiccator and reweigh. Repeat until constant mass is achieved. Calculate the moles of anhydrous salt and water. Example
12.5 g 12.5\mathrm{ g} 12.5 g of hydrated magnesium sulfate, MgSO4 _4 4 , ⋅ \cdot ⋅ xH2 _2 2 O, is heated to constant mass Of 6.1 g 6.1\mathrm{ g} 6.1 g .
Mass of water lost = 12.5 − 6.1 = 6.4 g = 12.5 - 6.1 = 6.4\mathrm{ g} = 12.5 − 6.1 = 6.4 g .
N ( M g S O 4 ) = 6.1 120.37 = 0.0507 m o l N(\mathrm{MgSO}_4) = \frac{6.1}{120.37} = 0.0507\mathrm{ mol} N ( MgSO 4 ) = 120.37 6.1 = 0.0507 mol N ( H 2 O ) = 6.4 18.02 = 0.355 m o l N(\mathrm{H}_2\mathrm{O}) = \frac{6.4}{18.02} = 0.355\mathrm{ mol} N ( H 2 O ) = 18.02 6.4 = 0.355 mol X = 0.355 0.0507 = 7.0 X = \frac{0.355}{0.0507} = 7.0 X = 0.0507 0.355 = 7.0 Formula: MgSO4 _4 4 , ⋅ \cdot ⋅ 7H_ 2 \_2 _2 O (Epsom salt).
Additional IB Exam-Style Questions Question 5 (Paper 2 style) 20.0 c m 3 20.0\mathrm{ cm}^3 20.0 cm 3 of 0.100 M 0.100\mathrm{ M} 0.100 M sulfuric acid is titrated with 0.200 M 0.200\mathrm{ M} 0.200 M sodium Hydroxide.
(a) Write the balanced equation.
H2 _2 2 SO4 _4 4 + 2NaOH → \to → Na2 _2 2 SO4 _4 4 + 2H2 _2 2 O
(b) Calculate the volume of NaOH needed to reach the equivalence point.
N ( H 2 S O 4 ) = 0.100 × 0.0200 = 0.00200 m o l N(\mathrm{H}_2\mathrm{SO}_4) = 0.100 \times 0.0200 = 0.00200\mathrm{ mol} N ( H 2 SO 4 ) = 0.100 × 0.0200 = 0.00200 mol Mole ratio: n ( N a O H ) = 2 × n ( H 2 S O 4 ) = 0.00400 m o l n(\mathrm{NaOH}) = 2 \times n(\mathrm{H}_2\mathrm{SO}_4) = 0.00400\mathrm{ mol} n ( NaOH ) = 2 × n ( H 2 SO 4 ) = 0.00400 mol .
V ( N a O H ) = 0.00400 0.200 = 0.0200 L = 20.0 c m 3 V(\mathrm{NaOH}) = \frac{0.00400}{0.200} = 0.0200\mathrm{ L} = 20.0\mathrm{ cm}^3 V ( NaOH ) = 0.200 0.00400 = 0.0200 L = 20.0 cm 3 (c) What is the pH at the equivalence point?
The salt Na2 _2 2 SO4 _4 4 is formed from a strong acid and strong base. The solution is neutral: pH = 7.
Question 6 (Paper 1 style) Which contains the greatest number of molecules?
A. 1 g 1\mathrm{ g} 1 g of H2 _2 2 B. 1 g 1\mathrm{ g} 1 g of O2 _2 2 C. 1 g 1\mathrm{ g} 1 g of N2 _2 2 D. 1 g 1\mathrm{ g} 1 g Of CO2 _2 2
Answer: A. Since n = m / M n = m/M n = m / M And H2 _2 2 has the smallest molar mass (2 g/mol), 1 g 1\mathrm{ g} 1 g of H2 _2 2 gives 0.5 m o l 0.5\mathrm{ mol} 0.5 mol Which is more moles (and thus more molecules) than the others.
Question 7 (Paper 2 style) Ammonia gas is produced by the reaction: N2 _2 2 (g) + 3H2 _2 2 (g) → \to → 2NH3 _3 3 (g).
If 56.0 g 56.0\mathrm{ g} 56.0 g of N2 _2 2 reacts with excess H2 _2 2 at 400 ° C 400\degree\mathrm{C} 400° C and 200 a t m 200\mathrm{ atm} 200 atm :
(a) Calculate the moles of NH3 _3 3 produced (assuming 100% yield).
N ( N 2 ) = 56.0 28.02 = 2.00 m o l N(\mathrm{N}_2) = \frac{56.0}{28.02} = 2.00\mathrm{ mol} N ( N 2 ) = 28.02 56.0 = 2.00 mol N ( N H 3 ) = 2 × 2.00 = 4.00 m o l N(\mathrm{NH}_3) = 2 \times 2.00 = 4.00\mathrm{ mol} N ( NH 3 ) = 2 × 2.00 = 4.00 mol (b) Calculate the volume of NH3 _3 3 at these conditions.
V = \frac`\{nRT}`{P} = \frac{4.00 \times 8.314 \times 673}{200 \times 101325} = \frac{22390}{20265000} = 1.105 \times 10^{-3}\mathrm{ m}^3 = 1.105\mathrm{ L} (c) If the actual yield is 3.20 m o l 3.20\mathrm{ mol} 3.20 mol Calculate the percentage yield.
P e r c e n t a g e y i e l d = 3.20 4.00 × 100 % = 80.0 % \mathrm{Percentage yield} = \frac{3.20}{4.00} \times 100\% = 80.0\% Percentageyield = 4.00 3.20 × 100% = 80.0% Stoichiometry: Extended Topics Back Titration A back titration is used when the analyte cannot be directly titrated. An excess of a standard Reagent is added, and the unreacted portion is titrated.
Example
An antacid tablet contains CaCO3 _3 3 . The tablet is dissolved in 50.0 c m 3 50.0\mathrm{ cm}^3 50.0 cm 3 of 0.200 M 0.200\mathrm{ M} 0.200 M HCl (excess). The remaining acid requires 30.0 c m 3 30.0\mathrm{ cm}^3 30.0 cm 3 of 0.100 M 0.100\mathrm{ M} 0.100 M NaOH for neutralisation.
Step 1 : Total moles of HCl added:
N ( H C l t o t a l ) = 0.200 × 0.0500 = 0.0100 m o l N(\mathrm{HCl}_{\mathrm{total}}) = 0.200 \times 0.0500 = 0.0100\mathrm{ mol} N ( HCl total ) = 0.200 × 0.0500 = 0.0100 mol Step 2 : Moles of HCl that reacted with NaOH:
N ( H C l u n r e a c t e d ) = n ( N a O H ) = 0.100 × 0.0300 = 0.00300 m o l N(\mathrm{HCl}_{\mathrm{unreacted}}) = n(\mathrm{NaOH}) = 0.100 \times 0.0300 = 0.00300\mathrm{ mol} N ( HCl unreacted ) = n ( NaOH ) = 0.100 × 0.0300 = 0.00300 mol Step 3 : Moles of HCl that reacted with CaCO3 _3 3 :
N ( H C l r e a c t e d ) = 0.0100 − 0.00300 = 0.00700 m o l N(\mathrm{HCl}_{\mathrm{reacted}}) = 0.0100 - 0.00300 = 0.00700\mathrm{ mol} N ( HCl reacted ) = 0.0100 − 0.00300 = 0.00700 mol Step 4 : Moles of CaCO3 _3 3 (ratio 1:2 with HCl):
N ( C a C O 3 ) = 0.00700 2 = 0.00350 m o l N(\mathrm{CaCO}_3) = \frac{0.00700}{2} = 0.00350\mathrm{ mol} N ( CaCO 3 ) = 2 0.00700 = 0.00350 mol Step 5 : Mass of CaCO3 _3 3 :
M = 0.00350 × 100.09 = 0.350 g M = 0.00350 \times 100.09 = 0.350\mathrm{ g} M = 0.00350 × 100.09 = 0.350 g Gravimetric Analysis Gravimetric analysis determines the amount of an analyte by measuring mass.
Steps :
Precipitate the analyte as an insoluble compound. Filter, wash, and dry the precipitate. Weigh the precipitate. Calculate the amount of analyte from stoichiometry. Example
A solution contains sulfate ions. BaCl2 _2 2 is added to precipitate BaSO4 _4 4 . The precipitate is Filtered, dried, and weighed at 0.582 g 0.582\mathrm{ g} 0.582 g .
N ( B a S O 4 ) = 0.582 233.39 = 0.00249 m o l N(\mathrm{BaSO}_4) = \frac{0.582}{233.39} = 0.00249\mathrm{ mol} N ( BaSO 4 ) = 233.39 0.582 = 0.00249 mol Since 1 mol BaSO4 _4 4 contains 1 mol SO4 2 − _4^{2-} 4 2 − :
M ( S O 4 2 − ) = 0.00249 × 96.06 = 0.239 g M(\mathrm{SO}_4^{2-}) = 0.00249 \times 96.06 = 0.239\mathrm{ g} M ( SO 4 2 − ) = 0.00249 × 96.06 = 0.239 g Gas Collection Methods Method Best For Gas Collected Downward displacement of water Insoluble gases Oxygen, hydrogen Upward delivery Soluble gases Ammonia Gas syringe Accurate volume Any gas Over water (eudiometer) Measuring volume Gases that do not dissolve
Ideal Gas Assumptions The ideal gas model assumes:
Gas particles have negligible volume. No intermolecular forces between particles. All collisions are perfectly elastic. Particles are in continuous random motion. Real gases deviate from ideal behaviour at high pressure and low temperature because:
Particle volume becomes significant. Intermolecular forces become significant. Additional IB Exam-Style Questions Question 8 (Paper 1 style) What volume of 0.500 M 0.500\mathrm{ M} 0.500 M H2 _2 2 SO4 _4 4 is required to completely neutralise 25.0 c m 3 25.0\mathrm{ cm}^3 25.0 cm 3 of 0.400 M 0.400\mathrm{ M} 0.400 M NaOH?
H 2 S O 4 + 2 N a O H → N a 2 S O 4 + 2 H 2 O \mathrm{H}_2\mathrm{SO}_4 + 2\mathrm{NaOH} \to \mathrm{Na}_2\mathrm{SO}_4 + 2\mathrm{H}_2\mathrm{O} H 2 SO 4 + 2 NaOH → Na 2 SO 4 + 2 H 2 O N ( N a O H ) = 0.400 × 0.0250 = 0.0100 m o l N(\mathrm{NaOH}) = 0.400 \times 0.0250 = 0.0100\mathrm{ mol} N ( NaOH ) = 0.400 × 0.0250 = 0.0100 mol N ( H 2 S O 4 ) = 0.0100 2 = 0.00500 m o l N(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.0100}{2} = 0.00500\mathrm{ mol} N ( H 2 SO 4 ) = 2 0.0100 = 0.00500 mol V ( H 2 S O 4 ) = 0.00500 0.500 = 0.0100 L = 10.0 c m 3 V(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00500}{0.500} = 0.0100\mathrm{ L} = 10.0\mathrm{ cm}^3 V ( H 2 SO 4 ) = 0.500 0.00500 = 0.0100 L = 10.0 cm 3 Question 9 (Paper 2 style) A mixture of NaHCO3 _3 3 and NaCl has a total mass of 4.68 g 4.68\mathrm{ g} 4.68 g . When heated, only NaHCO3 _3 3 Decomposes:
2 N a H C O 3 → N a 2 C O 3 + H 2 O + C O 2 2\mathrm{NaHCO}_3 \to \mathrm{Na}_2\mathrm{CO}_3 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2 2 NaHCO 3 → Na 2 CO 3 + H 2 O + CO 2 The mass loss is 1.32 g 1.32\mathrm{ g} 1.32 g . Find the percentage of NaHCO3 _3 3 in the mixture.
The mass loss is due to H2 _2 2 O + CO2 _2 2 (18 + 44 = 62 g / m o l 18 + 44 = 62\mathrm{ g/mol} 18 + 44 = 62 g/mol for each 2 mol NaHCO3 _3 3 Or 31 g / m o l 31\mathrm{ g/mol} 31 g/mol per mole of NaHCO3 _3 3 ).
N ( N a H C O 3 ) = 1.32 31 = 0.0426 m o l N(\mathrm{NaHCO}_3) = \frac{1.32}{31} = 0.0426\mathrm{ mol} N ( NaHCO 3 ) = 31 1.32 = 0.0426 mol M ( N a H C O 3 ) = 0.0426 × 84.01 = 3.58 g M(\mathrm{NaHCO}_3) = 0.0426 \times 84.01 = 3.58\mathrm{ g} M ( NaHCO 3 ) = 0.0426 × 84.01 = 3.58 g % N a H C O 3 = 3.58 4.68 × 100 % = 76.5 % \%\mathrm{NaHCO}_3 = \frac{3.58}{4.68} \times 100\% = 76.5\% % NaHCO 3 = 4.68 3.58 × 100% = 76.5% Question 10 (Paper 1 style) Avogadro’s constant is 6.02 × 10 23 6.02 \times 10^{23} 6.02 × 1 0 23 . What is the number of oxygen atoms in 0.050 m o l 0.050\mathrm{ mol} 0.050 mol of Al2 _2 2 (SO4 _4 4 )3 _3 3 ?
N ( O ) = 0.050 × 12 = 0.60 m o l N(\mathrm{O}) = 0.050 \times 12 = 0.60\mathrm{ mol} N ( O ) = 0.050 × 12 = 0.60 mol N u m b e r o f O a t o m s = 0.60 × 6.02 × 10 23 = 3.61 × 10 23 \mathrm{Number of O atoms} = 0.60 \times 6.02 \times 10^{23} = 3.61 \times 10^{23} NumberofOatoms = 0.60 × 6.02 × 1 0 23 = 3.61 × 1 0 23 Practice Problems Question 1: Empirical and Molecular Formula A compound contains 40.0 % 40.0\% 40.0% carbon, 6.7 % 6.7\% 6.7% hydrogen, and 53.3 % 53.3\% 53.3% oxygen by mass. Its molar mass Is approximately 180 g / m o l 180\mathrm{ g/mol} 180 g/mol . Determine the empirical and molecular formulas.
Answer Convert percentages to moles:
Element Mass (g) Molar Mass (g/mol) Moles Ratio C 40.0 40.0 40.0 12.01 12.01 12.01 3.33 3.33 3.33 1 1 1 H 6.7 6.7 6.7 1.01 1.01 1.01 6.63 6.63 6.63 2 2 2 O 53.3 53.3 53.3 16.00 16.00 16.00 3.33 3.33 3.33 1 1 1
Empirical formula: C H 2 O \mathrm{CH}_2\mathrm{O} CH 2 O (molar mass = 30.03 g / m o l = 30.03\mathrm{ g/mol} = 30.03 g/mol )
n = 180 30.03 ≈ 6 n = \frac{180}{30.03} \approx 6 n = 30.03 180 ≈ 6
Molecular formula: C 6 H 12 O 6 \mathrm{C}_6\mathrm{H}_{12}\mathrm{O}_6 C 6 H 12 O 6 (glucose)
Question 2: Limiting Reagent and Percentage Yield 8.0 g 8.0\mathrm{ g} 8.0 g of C a C O 3 \mathrm{CaCO}_3 CaCO 3 is heated with excess H C l \mathrm{HCl} HCl according to:
C a C O 3 + 2 H C l → C a C l 2 + H 2 O + C O 2 \mathrm{CaCO}_3 + 2\mathrm{HCl} \to \mathrm{CaCl}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2 CaCO 3 + 2 HCl → CaCl 2 + H 2 O + CO 2
(a) Calculate the theoretical volume of C O 2 \mathrm{CO}_2 CO 2 produced at RTP.
(b) If only 1.60 L 1.60\mathrm{ L} 1.60 L of C O 2 \mathrm{CO}_2 CO 2 is collected, calculate the percentage yield.
Answer (a) n ( C a C O 3 ) = 8.0 100.09 = 0.0800 m o l n(\mathrm{CaCO}_3) = \frac{8.0}{100.09} = 0.0800\mathrm{ mol} n ( CaCO 3 ) = 100.09 8.0 = 0.0800 mol
n ( C O 2 ) = 0.0800 m o l n(\mathrm{CO}_2) = 0.0800\mathrm{ mol} n ( CO 2 ) = 0.0800 mol (1:1 ratio)
V t h e o r e t i c a l = 0.0800 × 24.8 = 1.98 L V_{\mathrm{theoretical}} = 0.0800 \times 24.8 = 1.98\mathrm{ L} V theoretical = 0.0800 × 24.8 = 1.98 L
(b) % y i e l d = 1.60 1.98 × 100 % = 80.8 % \%\mathrm{ yield} = \frac{1.60}{1.98} \times 100\% = 80.8\% % yield = 1.98 1.60 × 100% = 80.8%
Question 3: Ideal Gas Law A gas occupies 3.00 L 3.00\mathrm{ L} 3.00 L at 350 K 350\mathrm{ K} 350 K and 150 k P a 150\mathrm{ kPa} 150 kPa . What volume does it Occupy at STP (273 K 273\mathrm{ K} 273 K , 100 k P a 100\mathrm{ kPa} 100 kPa )?
Answer P 1 V 1 T 1 = P 2 V 2 T 2 \frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2} T 1 P 1 V 1 = T 2 P 2 V 2
V 2 = P 1 V 1 T 2 P 2 T 1 = 150 × 3.00 × 273 100 × 350 = 122850 35000 = 3.51 L V_2 = \frac{P_1 V_1 T_2}{P_2 T_1} = \frac{150 \times 3.00 \times 273}{100 \times 350} = \frac{122850}{35000} = 3.51\mathrm{ L} V 2 = P 2 T 1 P 1 V 1 T 2 = 100 × 350 150 × 3.00 × 273 = 35000 122850 = 3.51 L
Question 4: Titration Calculation 25.0 c m 3 25.0\mathrm{ cm}^3 25.0 cm 3 of sulfuric acid is titrated with 0.200 M 0.200\mathrm{ M} 0.200 M N a O H \mathrm{NaOH} NaOH . The Endpoint is reached at 30.0 c m 3 30.0\mathrm{ cm}^3 30.0 cm 3 of N a O H \mathrm{NaOH} NaOH . Calculate the concentration of the Sulfuric acid.
Answer H 2 S O 4 + 2 N a O H → N a 2 S O 4 + 2 H 2 O \mathrm{H}_2\mathrm{SO}_4 + 2\mathrm{NaOH} \to \mathrm{Na}_2\mathrm{SO}_4 + 2\mathrm{H}_2\mathrm{O} H 2 SO 4 + 2 NaOH → Na 2 SO 4 + 2 H 2 O
n ( N a O H ) = 0.200 × 0.0300 = 0.00600 m o l n(\mathrm{NaOH}) = 0.200 \times 0.0300 = 0.00600\mathrm{ mol} n ( NaOH ) = 0.200 × 0.0300 = 0.00600 mol
n ( H 2 S O 4 ) = 0.00600 2 = 0.00300 m o l n(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00600}{2} = 0.00300\mathrm{ mol} n ( H 2 SO 4 ) = 2 0.00600 = 0.00300 mol
c ( H 2 S O 4 ) = 0.00300 0.0250 = 0.120 m o l / L c(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00300}{0.0250} = 0.120\mathrm{ mol/L} c ( H 2 SO 4 ) = 0.0250 0.00300 = 0.120 mol/L
Question 5: Water of Crystallisation 6.44 g 6.44\mathrm{ g} 6.44 g of hydrated magnesium sulfate M g S O 4 ⋅ x H 2 O \mathrm{MgSO}_4 \cdot x\mathrm{H}_2\mathrm{O} MgSO 4 ⋅ x H 2 O is Heated to constant mass of 3.14 g 3.14\mathrm{ g} 3.14 g . Determine the value of x x x .
Answer Mass of water lost = 6.44 − 3.14 = 3.30 g = 6.44 - 3.14 = 3.30\mathrm{ g} = 6.44 − 3.14 = 3.30 g
n ( M g S O 4 ) = 3.14 120.37 = 0.0261 m o l n(\mathrm{MgSO}_4) = \frac{3.14}{120.37} = 0.0261\mathrm{ mol} n ( MgSO 4 ) = 120.37 3.14 = 0.0261 mol
n ( H 2 O ) = 3.30 18.02 = 0.183 m o l n(\mathrm{H}_2\mathrm{O}) = \frac{3.30}{18.02} = 0.183\mathrm{ mol} n ( H 2 O ) = 18.02 3.30 = 0.183 mol
x = 0.183 0.0261 = 7.01 ≈ 7 x = \frac{0.183}{0.0261} = 7.01 \approx 7 x = 0.0261 0.183 = 7.01 ≈ 7
Formula: M g S O 4 ⋅ 7 H 2 O \mathrm{MgSO}_4 \cdot 7\mathrm{H}_2\mathrm{O} MgSO 4 ⋅ 7 H 2 O (Epsom salt)
For the A-Level treatment of this topic, see Quantitative Chemistry .
Common Pitfalls Forgetting to balance equations before performing calculations — always check that atoms and charges balance on both sides.
Assuming that a strong acid always has a lower pH than a weak acid without considering concentration.
Misidentifying the limiting reagent — compare mole ratios rather than comparing masses.
Confusing enthalpy of formation with enthalpy of combustion, or using the wrong sign convention.
Cross-References Topic Site Link [Stoichiometry] A-Level View [Stoichiometry] IB View [Stoichiometry] DSE View
Worked Examples Worked examples demonstrating the application of key concepts are covered in the detailed sub-pages
l i n k e d a b o v e . linked above. l ink e d ab o v e .