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Stoichiometry

The Mole Concept

Definition

The mole is the SI unit for amount of substance. One mole contains exactly 6.022×10236.022 \times 10^{23} elementary entities (atoms, molecules, ions, etc.).

Avogadro”s Constant

NA=6.022×1023mol1N_A = 6.022 \times 10^{23}\mathrm{ mol}^{-1}

The number of particles NN in nn moles:

N=n×NAN = n \times N_A

Molar Mass

The molar mass MM is the mass of one mole of a substance, expressed in g/mol\mathrm{g/mol}.

N=mMN = \frac{m}{M}

Where mm is the mass in grams.

SubstanceMolar Mass (g/mol)
H1.01
C12.01
N14.01
O16.00
Na22.99
Cl35.45
H2_2O18.02
CO2_244.01
NaCl58.44
H2_2SO4_498.08

Example

Calculate the number of molecules in 5.0g5.0\mathrm{ g} of water.

N=mM=5.018.02=0.278molN = \frac{m}{M} = \frac{5.0}{18.02} = 0.278\mathrm{ mol}N=0.278×6.022×1023=1.67×1023moleculesN = 0.278 \times 6.022 \times 10^{23} = 1.67 \times 10^{23}\mathrm{ molecules}

Empirical and Molecular Formulas

Empirical Formula

The empirical formula gives the simplest whole-number ratio of atoms in a compound.

Molecular Formula

The molecular formula gives the actual number of atoms of each element in a molecule.

Molecularformula=(Empiricalformula)n\mathrm{Molecular formula} = (\mathrm{Empirical formula})_n

Where nn is an integer.

Finding the Empirical Formula

  1. Find the mass (or percentage) of each element.
  2. Convert masses to moles: n=mMn = \dfrac{m}{M}.
  3. Divide all mole values by the smallest mole value.
  4. Round to the nearest whole number (or multiply to get integers).
  5. Write the empirical formula.

Example

A compound contains 40.0%40.0\% carbon, 6.7%6.7\% hydrogen, and 53.3%53.3\% oxygen by mass. Find its Empirical formula.

ElementMass (g)Molar Mass (g/mol)MolesRatio
C40.012.013.331
H6.71.016.632
O53.316.003.331

Empirical formula: CH2_2O.

If the molar mass is 180g/mol180\mathrm{ g/mol}The molecular formula is:

N=18030.03=6N = \frac{180}{30.03} = 6

Molecular formula: C6_6H12_{12}O6_6 (glucose).

Hydrated Salts

A hydrated salt contains water of crystallisation. The formula is written as, for example, CuSO4_4, \cdot5H_2\_2O.

To find the number of water molecules:

  1. Heat the hydrated salt to remove water.
  2. Measure the mass loss.
  3. Calculate moles of anhydrous salt and moles of water.
  4. Find the ratio.

Example

12.5g12.5\mathrm{ g} of hydrated copper(II) sulfate, CuSO4_4, \cdotxH2_2O, is heated to give 8.0g8.0\mathrm{ g} of anhydrous CuSO4_4. Find xx.

Mass of water lost =12.58.0=4.5g= 12.5 - 8.0 = 4.5\mathrm{ g}.

N(CuSO4)=8.0159.61=0.0501molN(\mathrm{CuSO}_4) = \frac{8.0}{159.61} = 0.0501\mathrm{ mol}N(H2O)=4.518.02=0.250molN(\mathrm{H}_2\mathrm{O}) = \frac{4.5}{18.02} = 0.250\mathrm{ mol}X=0.2500.0501=4.995X = \frac{0.250}{0.0501} = 4.99 \approx 5

Formula: CuSO4_4, \cdot5H_2\_2O.


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

  1. Write the unbalanced equation with correct formulas.
  2. Count atoms of each element on both sides.
  3. Balance one element at a time using coefficients.
  4. Leave hydrogen and oxygen until last.
  5. Check that all elements are balanced.
  6. Ensure coefficients are in the lowest whole-number ratio.

Example

Balance the combustion of propane:

Unbalanced: C3_3H8_8 + O2_2 \to CO2_2 + H2_2O

Balance C: C3_3H8_8 + O2_2 \to 3CO2_2 + H2_2O

Balance H: C3_3H8_8 + O2_2 \to 3CO2_2 + 4H2_2O

Balance O: C3_3H8_8 + 5O2_2 \to 3CO2_2 + 4H2_2O

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(aq) + NaCl(aq) \to AgCl(s) + NaNO3_3(aq)

Full ionic: Ag+^+(aq) + NO3_3^- + Na+^+ + Cl^- \to AgCl(s) + Na+^+ + NO3_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

  1. Calculate moles of each reactant.
  2. Determine which reactant is limiting (divide moles by stoichiometric coefficient).
  3. Use the limiting reagent to calculate the amount of product.

Example

5.0g5.0\mathrm{ g} of iron reacts with 3.0g3.0\mathrm{ g} of sulfur: Fe + S \to FeS.

N(Fe)=5.055.85=0.0895molN(\mathrm{Fe}) = \frac{5.0}{55.85} = 0.0895\mathrm{ mol}N(S)=3.032.07=0.0936molN(\mathrm{S}) = \frac{3.0}{32.07} = 0.0936\mathrm{ mol}

Stoichiometric ratio is 1:1, so Fe is the limiting reagent (fewer moles).

N(FeS)=0.0895molN(\mathrm{FeS}) = 0.0895\mathrm{ mol}M(FeS)=0.0895×87.91=7.87gM(\mathrm{FeS}) = 0.0895 \times 87.91 = 7.87\mathrm{ g}

Percentage Yield

Percentageyield=actualyieldtheoreticalyield×100%\mathrm{Percentage yield} = \frac{\mathrm{actual yield}}{\mathrm{theoretical yield}} \times 100\%

Example

If 6.5g6.5\mathrm{ g} of FeS was actually produced in the previous example:

Percentageyield=6.57.87×100%=82.6%\mathrm{Percentage yield} = \frac{6.5}{7.87} \times 100\% = 82.6\%

Gas Laws

Boyle’s Law (Constant Temperature)

For a fixed amount of gas at constant temperature:

P1V1=P2V2P_1 V_1 = P_2 V_2

Pressure is inversely proportional to volume: P1VP \propto \dfrac{1}{V}.

Charles’s Law (Constant Pressure)

For a fixed amount of gas at constant pressure:

V1T1=V2T2\frac{V_1}{T_1} = \frac{V_2}{T_2}

(Temperature must be in Kelvin.)

Volume is directly proportional to absolute temperature: VTV \propto T.

Gay-Lussac’s Law (Constant Volume)

For a fixed amount of gas at constant volume:

P1T1=P2T2\frac{P_1}{T_1} = \frac{P_2}{T_2}

Pressure is directly proportional to absolute temperature: PTP \propto T.

The Ideal Gas Equation

Combining all three laws:

PV=nRTPV = nRT

Where:

  • PP = pressure (Pa)
  • VV = volume (m3^3)
  • nn = number of moles
  • RR = universal gas constant =8.314J/(molK)= 8.314\mathrm{ J/(mol}\cdot\mathrm{K)}
  • TT = temperature (K)

Molar Volume

At STP (0°C0\degree\mathrm{C}, 100kPa100\mathrm{ kPa}), one mole of any ideal gas occupies 22.7L22.7\mathrm{ L}.

At RTP (25°C25\degree\mathrm{C}, 100kPa100\mathrm{ kPa}), one mole occupies 24.8L24.8\mathrm{ L}.

Example

Calculate the volume occupied by 2.5mol2.5\mathrm{ mol} of gas at 25°C25\degree\mathrm{C} and 1.2atm1.2\mathrm{ atm}.

P=1.2×101325=121590PaP = 1.2 \times 101325 = 121590\mathrm{ Pa}T=298KT = 298\mathrm{ 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+an2V2) ⁣(Vnb)=nRT\left(P + \frac{a n^2}{V^2}\right)\!\left(V - nb\right) = nRT

Where aa accounts for intermolecular attractions and bb accounts for molecular volume.

Kinetic Molecular Theory Assumptions

  1. Gas particles have negligible volume.
  2. Gas particles exert no forces on each other.
  3. All collisions are perfectly elastic.
  4. The average kinetic energy is proportional to temperature: Eˉk=32kBT\bar{E}_k = \dfrac{3}{2}k_BT.

Solution Chemistry

Concentration

Molarity

C=nVC = \frac{n}{V}

Where cc is in mol/L\mathrm{mol/L} (or M), nn in mol, and VV in L.

Molality

B=nsolutemsolventB = \frac{n_{\mathrm{solute}}}{m_{\mathrm{solvent}}}

Where bb is in mol/kg\mathrm{mol/kg}.

Mass Percentage

%=msolutemsolution×100%\% = \frac{m_{\mathrm{solute}}}{m_{\mathrm{solution}}} \times 100\%

Parts Per Million (ppm)

ppm=msolutemsolution×106\mathrm{ppm} = \frac{m_{\mathrm{solute}}}{m_{\mathrm{solution}}} \times 10^6

Example

What is the concentration of a solution made by dissolving 10.0g10.0\mathrm{ g} of NaCl in enough water To make 250mL250\mathrm{ mL} of solution?

N=10.058.44=0.171molN = \frac{10.0}{58.44} = 0.171\mathrm{ mol}C=0.1710.250=0.684mol/LC = \frac{0.171}{0.250} = 0.684\mathrm{ mol/L}

Dilution

C1V1=c2V2C_1 V_1 = c_2 V_2

Example

What volume of 6.0M6.0\mathrm{ M} HCl is needed to make 500mL500\mathrm{ mL} of 0.50M0.50\mathrm{ M} HCl?

V1=c2V2c1=0.50×5006.0=41.7mLV_1 = \frac{c_2 V_2}{c_1} = \frac{0.50 \times 500}{6.0} = 41.7\mathrm{ mL}

Standard Solutions

A standard solution is one of accurately known concentration. To prepare:

  1. Calculate the mass of solute needed.
  2. Accurately weigh the solute.
  3. Dissolve in a small amount of solvent.
  4. Transfer to a volumetric flask.
  5. 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

25.0mL25.0\mathrm{ mL} of NaOH is titrated with 0.100M0.100\mathrm{ M} HCl. The endpoint is reached at 20.0mL20.0\mathrm{ mL} of HCl. Find the concentration of NaOH.

NaOH+HClNaCl+H2O\mathrm{NaOH} + \mathrm{HCl} \to \mathrm{NaCl} + \mathrm{H}_2\mathrm{O}N(HCl)=0.100×0.0200=0.00200molN(\mathrm{HCl}) = 0.100 \times 0.0200 = 0.00200\mathrm{ mol}

Stoichiometry 1:1, so n(NaOH)=0.00200moln(\mathrm{NaOH}) = 0.00200\mathrm{ mol}.

C(NaOH)=0.002000.0250=0.0800MC(\mathrm{NaOH}) = \frac{0.00200}{0.0250} = 0.0800\mathrm{ M}

IB Exam-Style Questions

Question 1 (Paper 1 style)

What is the empirical formula of a compound that is 36.5%36.5\% sodium, 25.4%25.4\% sulfur, and 38.1%38.1\% Oxygen?

ElementMass (g)Molar MassMolesRatio
Na36.522.991.5882
S25.432.070.7921
O38.116.002.3813

Empirical formula: Na2_2SO3_3.

Question 2 (Paper 2 style)

10.0g10.0\mathrm{ g} of calcium carbonate (CaCO3_3) is heated until completely decomposed: CaCO3_3 \to CaO + CO2_2.

(a) Calculate the volume of CO2_2 produced at RTP.

N(CaCO3)=10.0100.09=0.0999molN(\mathrm{CaCO}_3) = \frac{10.0}{100.09} = 0.0999\mathrm{ mol}N(CO2)=0.0999molN(\mathrm{CO}_2) = 0.0999\mathrm{ mol}V=n×24.8=0.0999×24.8=2.48LV = n \times 24.8 = 0.0999 \times 24.8 = 2.48\mathrm{ L}

(b) Calculate the mass of CaO produced.

M(CaO)=0.0999×56.08=5.60gM(\mathrm{CaO}) = 0.0999 \times 56.08 = 5.60\mathrm{ g}

Question 3 (Paper 1 style)

A gas at 300K300\mathrm{ K} and 1.5atm1.5\mathrm{ atm} occupies 4.0L4.0\mathrm{ L}. What volume does it Occupy at 350K350\mathrm{ K} and 2.0atm2.0\mathrm{ atm}?

P1V1T1=P2V2T2\frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2}V2=P1V1T2P2T1=1.5×4.0×3502.0×300=2100600=3.5LV_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}

Question 4 (Paper 2 style)

3.0g3.0\mathrm{ g} of magnesium reacts with excess hydrochloric acid: Mg + 2HCl \to MgCl2_2 + H2_2.

(a) Calculate the moles of hydrogen gas produced.

N(Mg)=3.024.31=0.123molN(\mathrm{Mg}) = \frac{3.0}{24.31} = 0.123\mathrm{ mol}N(H2)=0.123mol(1:1ratio)N(\mathrm{H}_2) = 0.123\mathrm{ mol} \mathrm{ (1:1 ratio)}

(b) Calculate the volume of H2_2 at STP.

V=0.123×22.7=2.79LV = 0.123 \times 22.7 = 2.79\mathrm{ L}

(c) If only 2.5L2.5\mathrm{ L} of H2_2 was collected, calculate the percentage yield.

Percentageyield=2.52.79×100%=89.6%\mathrm{Percentage yield} = \frac{2.5}{2.79} \times 100\% = 89.6\%

Summary

FormulaExpression
Moles from massn=mMn = \dfrac{m}{M}
ParticlesN=nNAN = nN_A
Molarityc=nVc = \dfrac{n}{V}
Ideal gasPV=nRTPV = nRT
Boyle’s lawP1V1=P2V2P_1V_1 = P_2V_2
Charles’s lawV1T1=V2T2\dfrac{V_1}{T_1} = \dfrac{V_2}{T_2}
Dilutionc1V1=c2V2c_1V_1 = c_2V_2
Percentage yieldactualtheoretical×100%\dfrac{\mathrm{actual}}{\mathrm{theoretical}} \times 100\%

Example

Compare the rates of diffusion of He (4 g/mol) and O2_2 (32 g/mol).

rHerO2=324=8=2.83\frac{r_{\mathrm{He}}}{r_{\mathrm{O}_2}} = \sqrt{\frac{32}{4}} = \sqrt{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 1.43g/L1.43\mathrm{ g/L} at STP. Find its molar mass.

M=ρRTP=1.43×8.314×273101325=3247101325=0.0320kg/mol=32.0g/molM = \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}

The gas is likely O2_2.


Solutions: Extended

Concentration Conversions

FromToMethod
MolarityMass percentagec×M×100/(1000ρ)c \times M \times 100 / (1000\rho)
Mass percentageMolarity(%/100)×ρ×1000/M(\%\mathrm{/}100) \times \rho \times 1000 / M
Molarityppmc×M×106/1000ρc \times M \times 10^6 / 1000\rho

Colligative Properties

Properties that depend on the number of solute particles (not their identity):

  1. Boiling point elevation: ΔTb=iKb×m\Delta T_b = iK_b \times m
  2. Freezing point depression: ΔTf=iKf×m\Delta T_f = iK_f \times m
  3. Osmotic pressure: Π=icRT\Pi = icRT

Where ii is the van’t Hoff factor (number of particles per formula unit), KbK_b and KfK_f are Constants, and mm is molality.

Soluteii
Non-electrolyte (e.g., glucose)1
NaCl2
CaCl2_23

Water of Crystallisation: Extended

Determining the Formula of a Hydrate

Procedure:

  1. Weigh the hydrated salt.
  2. Heat gently to drive off water.
  3. Cool in a desiccator and reweigh.
  4. Repeat until constant mass is achieved.
  5. Calculate the moles of anhydrous salt and water.

Example

12.5g12.5\mathrm{ g} of hydrated magnesium sulfate, MgSO4_4, \cdotxH2_2O, is heated to constant mass Of 6.1g6.1\mathrm{ g}.

Mass of water lost =12.56.1=6.4g= 12.5 - 6.1 = 6.4\mathrm{ g}.

N(MgSO4)=6.1120.37=0.0507molN(\mathrm{MgSO}_4) = \frac{6.1}{120.37} = 0.0507\mathrm{ mol}N(H2O)=6.418.02=0.355molN(\mathrm{H}_2\mathrm{O}) = \frac{6.4}{18.02} = 0.355\mathrm{ mol}X=0.3550.0507=7.0X = \frac{0.355}{0.0507} = 7.0

Formula: MgSO4_4, \cdot7H_2\_2O (Epsom salt).


Additional IB Exam-Style Questions

Question 5 (Paper 2 style)

20.0cm320.0\mathrm{ cm}^3 of 0.100M0.100\mathrm{ M} sulfuric acid is titrated with 0.200M0.200\mathrm{ M} sodium Hydroxide.

(a) Write the balanced equation.

H2_2SO4_4 + 2NaOH \to Na2_2SO4_4 + 2H2_2O

(b) Calculate the volume of NaOH needed to reach the equivalence point.

N(H2SO4)=0.100×0.0200=0.00200molN(\mathrm{H}_2\mathrm{SO}_4) = 0.100 \times 0.0200 = 0.00200\mathrm{ mol}

Mole ratio: n(NaOH)=2×n(H2SO4)=0.00400moln(\mathrm{NaOH}) = 2 \times n(\mathrm{H}_2\mathrm{SO}_4) = 0.00400\mathrm{ mol}.

V(NaOH)=0.004000.200=0.0200L=20.0cm3V(\mathrm{NaOH}) = \frac{0.00400}{0.200} = 0.0200\mathrm{ L} = 20.0\mathrm{ cm}^3

(c) What is the pH at the equivalence point?

The salt Na2_2SO4_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. 1g1\mathrm{ g} of H2_2 B. 1g1\mathrm{ g} of O2_2 C. 1g1\mathrm{ g} of N2_2 D. 1g1\mathrm{ g} Of CO2_2

Answer: A. Since n=m/Mn = m/MAnd H2_2 has the smallest molar mass (2 g/mol), 1g1\mathrm{ g} of H2_2 gives 0.5mol0.5\mathrm{ 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(g) + 3H2_2(g) \to 2NH3_3(g).

If 56.0g56.0\mathrm{ g} of N2_2 reacts with excess H2_2 at 400°C400\degree\mathrm{C} and 200atm200\mathrm{ atm}:

(a) Calculate the moles of NH3_3 produced (assuming 100% yield).

N(N2)=56.028.02=2.00molN(\mathrm{N}_2) = \frac{56.0}{28.02} = 2.00\mathrm{ mol}N(NH3)=2×2.00=4.00molN(\mathrm{NH}_3) = 2 \times 2.00 = 4.00\mathrm{ mol}

(b) Calculate the volume of NH3_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 3.20mol3.20\mathrm{ mol}Calculate the percentage yield.

Percentageyield=3.204.00×100%=80.0%\mathrm{Percentage yield} = \frac{3.20}{4.00} \times 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. The tablet is dissolved in 50.0cm350.0\mathrm{ cm}^3 of 0.200M0.200\mathrm{ M} HCl (excess). The remaining acid requires 30.0cm330.0\mathrm{ cm}^3 of 0.100M0.100\mathrm{ M} NaOH for neutralisation.

Step 1: Total moles of HCl added:

N(HCltotal)=0.200×0.0500=0.0100molN(\mathrm{HCl}_{\mathrm{total}}) = 0.200 \times 0.0500 = 0.0100\mathrm{ mol}

Step 2: Moles of HCl that reacted with NaOH:

N(HClunreacted)=n(NaOH)=0.100×0.0300=0.00300molN(\mathrm{HCl}_{\mathrm{unreacted}}) = n(\mathrm{NaOH}) = 0.100 \times 0.0300 = 0.00300\mathrm{ mol}

Step 3: Moles of HCl that reacted with CaCO3_3:

N(HClreacted)=0.01000.00300=0.00700molN(\mathrm{HCl}_{\mathrm{reacted}}) = 0.0100 - 0.00300 = 0.00700\mathrm{ mol}

Step 4: Moles of CaCO3_3 (ratio 1:2 with HCl):

N(CaCO3)=0.007002=0.00350molN(\mathrm{CaCO}_3) = \frac{0.00700}{2} = 0.00350\mathrm{ mol}

Step 5: Mass of CaCO3_3:

M=0.00350×100.09=0.350gM = 0.00350 \times 100.09 = 0.350\mathrm{ g}

Gravimetric Analysis

Gravimetric analysis determines the amount of an analyte by measuring mass.

Steps:

  1. Precipitate the analyte as an insoluble compound.
  2. Filter, wash, and dry the precipitate.
  3. Weigh the precipitate.
  4. Calculate the amount of analyte from stoichiometry.

Example

A solution contains sulfate ions. BaCl2_2 is added to precipitate BaSO4_4. The precipitate is Filtered, dried, and weighed at 0.582g0.582\mathrm{ g}.

N(BaSO4)=0.582233.39=0.00249molN(\mathrm{BaSO}_4) = \frac{0.582}{233.39} = 0.00249\mathrm{ mol}

Since 1 mol BaSO4_4 contains 1 mol SO42_4^{2-}:

M(SO42)=0.00249×96.06=0.239gM(\mathrm{SO}_4^{2-}) = 0.00249 \times 96.06 = 0.239\mathrm{ g}

Gas Collection Methods

MethodBest ForGas Collected
Downward displacement of waterInsoluble gasesOxygen, hydrogen
Upward deliverySoluble gasesAmmonia
Gas syringeAccurate volumeAny gas
Over water (eudiometer)Measuring volumeGases that do not dissolve

Ideal Gas Assumptions

The ideal gas model assumes:

  1. Gas particles have negligible volume.
  2. No intermolecular forces between particles.
  3. All collisions are perfectly elastic.
  4. 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 0.500M0.500\mathrm{ M} H2_2SO4_4 is required to completely neutralise 25.0cm325.0\mathrm{ cm}^3 of 0.400M0.400\mathrm{ M} NaOH?

H2SO4+2NaOHNa2SO4+2H2O\mathrm{H}_2\mathrm{SO}_4 + 2\mathrm{NaOH} \to \mathrm{Na}_2\mathrm{SO}_4 + 2\mathrm{H}_2\mathrm{O}N(NaOH)=0.400×0.0250=0.0100molN(\mathrm{NaOH}) = 0.400 \times 0.0250 = 0.0100\mathrm{ mol}N(H2SO4)=0.01002=0.00500molN(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.0100}{2} = 0.00500\mathrm{ mol}V(H2SO4)=0.005000.500=0.0100L=10.0cm3V(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00500}{0.500} = 0.0100\mathrm{ L} = 10.0\mathrm{ cm}^3

Question 9 (Paper 2 style)

A mixture of NaHCO3_3 and NaCl has a total mass of 4.68g4.68\mathrm{ g}. When heated, only NaHCO3_3 Decomposes:

2NaHCO3Na2CO3+H2O+CO22\mathrm{NaHCO}_3 \to \mathrm{Na}_2\mathrm{CO}_3 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2

The mass loss is 1.32g1.32\mathrm{ g}. Find the percentage of NaHCO3_3 in the mixture.

The mass loss is due to H2_2O + CO2_2 (18+44=62g/mol18 + 44 = 62\mathrm{ g/mol} for each 2 mol NaHCO3_3Or 31g/mol31\mathrm{ g/mol} per mole of NaHCO3_3).

N(NaHCO3)=1.3231=0.0426molN(\mathrm{NaHCO}_3) = \frac{1.32}{31} = 0.0426\mathrm{ mol}M(NaHCO3)=0.0426×84.01=3.58gM(\mathrm{NaHCO}_3) = 0.0426 \times 84.01 = 3.58\mathrm{ g}%NaHCO3=3.584.68×100%=76.5%\%\mathrm{NaHCO}_3 = \frac{3.58}{4.68} \times 100\% = 76.5\%

Question 10 (Paper 1 style)

Avogadro’s constant is 6.02×10236.02 \times 10^{23}. What is the number of oxygen atoms in 0.050mol0.050\mathrm{ mol} of Al2_2(SO4_4)3_3?

N(O)=0.050×12=0.60molN(\mathrm{O}) = 0.050 \times 12 = 0.60\mathrm{ mol}NumberofOatoms=0.60×6.02×1023=3.61×1023\mathrm{Number of O atoms} = 0.60 \times 6.02 \times 10^{23} = 3.61 \times 10^{23}

Practice Problems

Question 1: Empirical and Molecular Formula

A compound contains 40.0%40.0\% carbon, 6.7%6.7\% hydrogen, and 53.3%53.3\% oxygen by mass. Its molar mass Is approximately 180g/mol180\mathrm{ g/mol}. Determine the empirical and molecular formulas.

Answer

Convert percentages to moles:

ElementMass (g)Molar Mass (g/mol)MolesRatio
C40.040.012.0112.013.333.3311
H6.76.71.011.016.636.6322
O53.353.316.0016.003.333.3311

Empirical formula: CH2O\mathrm{CH}_2\mathrm{O} (molar mass =30.03g/mol= 30.03\mathrm{ g/mol})

n=18030.036n = \frac{180}{30.03} \approx 6

Molecular formula: C6H12O6\mathrm{C}_6\mathrm{H}_{12}\mathrm{O}_6 (glucose)

Question 2: Limiting Reagent and Percentage Yield

8.0g8.0\mathrm{ g} of CaCO3\mathrm{CaCO}_3 is heated with excess HCl\mathrm{HCl} according to:

CaCO3+2HClCaCl2+H2O+CO2\mathrm{CaCO}_3 + 2\mathrm{HCl} \to \mathrm{CaCl}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{CO}_2

(a) Calculate the theoretical volume of CO2\mathrm{CO}_2 produced at RTP.

(b) If only 1.60L1.60\mathrm{ L} of CO2\mathrm{CO}_2 is collected, calculate the percentage yield.

Answer

(a) n(CaCO3)=8.0100.09=0.0800moln(\mathrm{CaCO}_3) = \frac{8.0}{100.09} = 0.0800\mathrm{ mol}

n(CO2)=0.0800moln(\mathrm{CO}_2) = 0.0800\mathrm{ mol} (1:1 ratio)

Vtheoretical=0.0800×24.8=1.98LV_{\mathrm{theoretical}} = 0.0800 \times 24.8 = 1.98\mathrm{ L}

(b) %yield=1.601.98×100%=80.8%\%\mathrm{ yield} = \frac{1.60}{1.98} \times 100\% = 80.8\%

Question 3: Ideal Gas Law

A gas occupies 3.00L3.00\mathrm{ L} at 350K350\mathrm{ K} and 150kPa150\mathrm{ kPa}. What volume does it Occupy at STP (273K273\mathrm{ K}, 100kPa100\mathrm{ kPa})?

Answer

P1V1T1=P2V2T2\frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2}

V2=P1V1T2P2T1=150×3.00×273100×350=12285035000=3.51LV_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}

Question 4: Titration Calculation

25.0cm325.0\mathrm{ cm}^3 of sulfuric acid is titrated with 0.200M0.200\mathrm{ M} NaOH\mathrm{NaOH}. The Endpoint is reached at 30.0cm330.0\mathrm{ cm}^3 of NaOH\mathrm{NaOH}. Calculate the concentration of the Sulfuric acid.

Answer

H2SO4+2NaOHNa2SO4+2H2O\mathrm{H}_2\mathrm{SO}_4 + 2\mathrm{NaOH} \to \mathrm{Na}_2\mathrm{SO}_4 + 2\mathrm{H}_2\mathrm{O}

n(NaOH)=0.200×0.0300=0.00600moln(\mathrm{NaOH}) = 0.200 \times 0.0300 = 0.00600\mathrm{ mol}

n(H2SO4)=0.006002=0.00300moln(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00600}{2} = 0.00300\mathrm{ mol}

c(H2SO4)=0.003000.0250=0.120mol/Lc(\mathrm{H}_2\mathrm{SO}_4) = \frac{0.00300}{0.0250} = 0.120\mathrm{ mol/L}

Question 5: Water of Crystallisation

6.44g6.44\mathrm{ g} of hydrated magnesium sulfate MgSO4xH2O\mathrm{MgSO}_4 \cdot x\mathrm{H}_2\mathrm{O} is Heated to constant mass of 3.14g3.14\mathrm{ g}. Determine the value of xx.

Answer

Mass of water lost =6.443.14=3.30g= 6.44 - 3.14 = 3.30\mathrm{ g}

n(MgSO4)=3.14120.37=0.0261moln(\mathrm{MgSO}_4) = \frac{3.14}{120.37} = 0.0261\mathrm{ mol}

n(H2O)=3.3018.02=0.183moln(\mathrm{H}_2\mathrm{O}) = \frac{3.30}{18.02} = 0.183\mathrm{ mol}

x=0.1830.0261=7.017x = \frac{0.183}{0.0261} = 7.01 \approx 7

Formula: MgSO47H2O\mathrm{MgSO}_4 \cdot 7\mathrm{H}_2\mathrm{O} (Epsom salt)

For the A-Level treatment of this topic, see Quantitative Chemistry.

Common Pitfalls

  1. Forgetting to balance equations before performing calculations — always check that atoms and charges balance on both sides.

  2. Assuming that a strong acid always has a lower pH than a weak acid without considering concentration.

  3. Misidentifying the limiting reagent — compare mole ratios rather than comparing masses.

  4. Confusing enthalpy of formation with enthalpy of combustion, or using the wrong sign convention.

Cross-References

TopicSiteLink
[Stoichiometry]A-LevelView
[Stoichiometry]IBView
[Stoichiometry]DSEView

Worked Examples

Worked examples demonstrating the application of key concepts are covered in the detailed sub-pages

linkedabove.linked above.