Definitions [1]
Define the Stationary phase.
Stationary phase is a solid or a liquid supported on a solid which remains fixed in a place and on which different solutes are adsorbed to a different extent.
Key Points
- Organic compounds obtained from natural sources or prepared in the laboratory are usually impure.
- Purification is required to obtain compounds in a pure form for the study of physical and chemical properties.
- Impurities may be solids, liquids, or gases mixed with the compound.
- Different purification methods are used based on physical properties like solubility, boiling point, and volatility.
- The choice of method depends on the nature of the compound and impurity.
- Introduced by Tswett in 1906.
- Based on the difference in rates at which different components of a mixture move through a porous medium (stationary phase) under the influence of a solvent or gas (mobile or moving phase).
- The technique separates a mixture by distributing its components between one stationary phase and one mobile phase.
- Mobile phase determines the Rᶠ or R factor — dependent on the solubility of components in the given eluent.
Based on the fact that different compounds are adsorbed to different degrees on an adsorbent.
When a mobile phase (solvent) moves over the stationary phase, the components of the mixture move by different distances depending on their adsorption tendencies.
(i) Column Chromatography
- Adsorbent (alumina Al₂O₃, silica SiO₂, Fuller's earth) is packed as a column in a long, burette-like tube → acts as the stationary phase.
- Mixture dissolved in solvent → poured on top of column.
- The most strongly adsorbed component remains at the top.
- Solvent (eluent) is passed → components elute at different rates.
(ii) Thin Layer Chromatography (TLC)
- Separation of a mixture of substances over a thin layer of adsorbent coated on a glass plate.
- A glass plate is placed in a closed jar containing eluant.
- As the eluent rises, components move to different heights depending on their degree of adsorption → separation occurs.
Based on differences in the tendencies of substances to distribute or partition between the stationary phase and mobile phase.
Paper Chromatography
- A type of partition chromatography applied as a drop on paper.
- Paper is suspended in a suitable solvent or mixture → solvent rises by capillary action.
- Paper selectively retains different components according to their partition in the two phases.
- Colourless compounds are visualised using a ninhydrin spray (which forms coloured products).
Key terms:
- Stationary phase: The phase that is stationary with respect to the components of the mixture. In column chromatography, the stationary phase adsorbs components at different heights.
- Mobile phase (eluent): The phase that moves along with the components of the mixture.
Rᶠ Factor (Retardation Factor):
\[R_f=\frac{\text{Migration distance of substance}}{\text{Migration distance of solvent front}}\]
- Used to identify the product separated using paper or thin-layer chromatography.
- Rᶠ value is constant for a given compound under given conditions.
| Element | Method / Test | Principle | Observation | Inference |
|---|---|---|---|---|
| Carbon (C) | Copper oxide test | C oxidised to CO₂ by CuO | CO₂ turns lime water milky | Carbon present |
| Hydrogen (H) | Copper oxide test | H oxidised to H₂O by CuO | Anhydrous CuSO₄ turns blue | Hydrogen present |
| Nitrogen (N) | Lassaigne's test | Na + C + N → NaCN → Prussian blue with FeSO₄ + FeCl₃ | Prussian blue colour | Nitrogen present |
| Nitrogen + Sulphur (N+S) | Lassaigne's test | SCN⁻ formed instead of CN⁻ and S²⁻ separately | Blood red colour with FeCl₃ (Fe(SCN)²⁺) | Both N and S present |
| Sulphur (S) only | Sodium nitroprusside test | Na₂S + [Fe(CN)₅NO]²⁻ → coloured complex | Violet colour | Sulphur present |
| Chlorine (Cl) | Lassaigne's test + AgNO₃ | NaCl + AgNO₃ → AgCl↓ | White ppt, soluble in NH₄OH | Chlorine present |
| Bromine (Br) | Lassaigne's test + AgNO₃ | NaBr + AgNO₃ → AgBr↓ | Pale yellow ppt, partially soluble in NH₄OH | Bromine present |
| Iodine (I) | Lassaigne's test + AgNO₃ | NaI + AgNO₃ → AgI↓ | Yellow ppt, insoluble in NH₄OH | Iodine present |
| Halogen (Cl/Br) | Beilstein test | Organic compound on Cu wire in Bunsen flame | Green/blue-green flame | Halogen (Cl or Br) present |
| Phosphorus (P) | Ammonium molybdate test | P oxidised to phosphate → ammonium phosphomolybdate | Canary yellow ppt | Phosphorus present |
Estimation of Carbon and Hydrogen (Liebig's Combustion Method):
Principle: A known mass w gram of organic compound is heated strongly with an excess of dry CuO in a current of dry air or oxygen.
- Carbon oxidised to CO₂ (absorbed by KOH solution)
- Hydrogen oxidised to H₂O (absorbed by anhydrous CaCl₂)
Reactions:
- \[C+2CuO\xrightarrow{\text{strongly heat}}CO_2+2Cu\]
- \[2H+CuO\xrightarrow{\text{strongly heat}}H_2O+Cu\]
Formulas:
\[\%C=\frac{12\times\text{wt of }CO_2}{44\times\text{wt of organic compound}}\times100=\frac{12\times x\times100}{44\times w}=\frac{27.27\times x}{w}\]
\[\%H=\frac{2\times\mathrm{wt~of}H_2O}{18\times\text{wt of organic compound}}\times100=\frac{2\times y\times100}{18\times w}=\frac{11.11\times y}{w}\]
Where x = mass of CO₂ absorbed, y = mass of H₂O absorbed, and w = mass of organic compound.
Dumas Method:
- A known mass w gram of the organic compound is heated with cupric oxide in an atmosphere of carbon dioxide.
- Carbon and hydrogen are oxidised to CO₂ and H₂O.
- Sulphur oxidised to SO₂.
- Nitrogen is set free — any oxide of N is reduced to free N₂ by heated copper gauze.
- Gaseous mixture (CO₂, H₂O, N₂) collected over KOH solution → all gases except N₂ are absorbed.
- Volume of N₂ measured (V mL at STP).
\[\%N=\frac{28\times V\times100}{22400\times w}=\frac{0.125\times V}{w}\]
Nitrogen is estimated as gaseous nitrogen using Dumas' method.
Kjeldahl's Method:
Faster than Dumas' method.
Used only for organic compounds that are converted quantitatively to ammonium sulphate on heating strongly with concentrated sulphuric acid.
Cannot be used for compounds containing:
- Nitro (–NO₂) and diazo (–N=N⁻) groups
- Nitrogen in the ring (e.g., pyridine, quinoline)
Step 1 — Digestion: Organic compound digested with conc. H₂SO₄ in the presence of a small quantity of potassium sulphate and copper sulphate (in Kjeldahl's flask).
\[\text{Organic compound}+\mathrm{H}_{2}\mathrm{SO}_{4}\xrightarrow{CuSO_{4}+K_{2}SO_{4}}(\mathrm{NH}_{4})_{2}\mathrm{SO}_{4}\]
Step 2 — Distillation: (NH₄)₂SO₄ decomposed with excess NaOH → NH₃ liberated → absorbed in standard acid (say H₂SO₄) of known normality:
- V1 mL of N normality H₂SO₄ taken
- V2 mL of N normality NaOH used for back titration
- Volume of H₂SO₄ left used = V2 mL of N normality
\[\%N=\frac{1.4\times\text{Normality of acid}\times\text{Volume of acid used to neutralise }NH_3}{\text{Mass of the substance (w)}}\]
Carius Method:
Principle: A known mass of organic compound is heated with fuming nitric acid (HNO₃) in the presence of silver nitrate (AgNO₃) in a Carius tube → carbon and hydrogen oxidised to CO₂ and H₂O → halogen present reacts with AgNO₃ to form the corresponding silver halide (AgX).
Silver halide is filtered, washed, dried, and weighed.
Formulas:
\[\%X=\frac{\text{At wt of halogen}\times\text{wt of AgX formed}\times100}{\text{Mol. wt of silver halide}\times\text{wt of organic compound}}\]
\[\%Cl=\frac{35.5\times\text{wt of AgCl}\times100}{143.5\times w}=\frac{24.74\times\text{wt of AgCl}}{w}\]
\[\%Br=\frac{80}{188}\times\frac{\text{Mass of AgBr}\times100}{\text{Mass of compound}}=\frac{42.55\times\text{wt of AgBr}}{w}\]
\[\%I=\frac{127}{235}\times\frac{\text{Mass of AgI}\times100}{\text{Mass of compound}}=\frac{54\times\text{wt of AgI}}{w}\]
Messengers Method, Carius Method, and Fusion Method are the three methods for sulphur estimation.
Carius Method for Sulphur:
- A known mass ww gram of organic compound is heated with fuming HNO₃ or sodium peroxide (Na₂O₂) in a Carius tube → sulphur is oxidised to H₂SO₄.
- In the presence of BaCl₂ solution, sulphur is precipitated as BaSO₄ → filtered, dried, and weighed.
\[\%S=\frac{32\times\text{wt of BaSO}_4\times100}{233\times\text{wt of organic compound}}=\frac{13.73\times\text{wt of BaSO}_4\mathrm{ppt}}{w}\]
-
233 g BaSO₄ contains 32 g sulphur.
Carius (Second Method) for Phosphorus
- A known mass of organic compound is heated with fuming HNO₃ in a Carius tube → phosphorus is converted to H₃PO₄.
- Magnesium mixture (MgCl₂ + NH₄Cl) is added → gives precipitate of magnesium ammonium phosphate (MgNH₄PO₄) → on heating gives magnesium pyrophosphate (Mg₂P₂O₇) → weighed.
\[\%P=\frac{\text{Atomic mass of P}}{\text{Molecular mass of Mg}_2P_2O_7}\times\frac{\text{Mass of Mg}_2P_2O_7\times100}{\text{Mass of compound}}\]
\[=\frac{62}{222}\times\frac{\text{Mass of Mg}_2\mathrm{P}_2\mathrm{O}_2\quad100}{\text{Mass of compound}}\]
\[=\frac{27.93\times\text{wt of Mg}_2\mathrm{P}_2\mathrm{O}_7\mathrm{ppt}}{w}\]
Molecular mass of Mg₂P₂O₇ = 222 g; 2 atoms of P = 62 g.
Concepts [11]
- Purification of Organic Compounds
- Chromatography Method
- Chromatography Method > Adsorption Chromatography
- Chromatography Method > Partition Chromatography
- Qualitative Analysis of Organic Compounds
- Estimation of Carbon and Hydrogen
- Estimation of Nitrogen
- Estimation of Halogen
- Estimation of Sulphur
- Estimation of Phosphorous
- Important methods for determination of elements qualitatively and quantitatively
