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CS-991 · Module E-3
Complete Reaction Map
Exam Preparation Hub
🗺️ Ethanol → Ethene → Ethyne → Ethanal Chain
| Step | Reactant | Reagent / Condition | Product |
|---|---|---|---|
| 1 | Ethanol (C₂H₅OH) | Conc. H₂SO₄, heat (dehydration) | Ethene (C₂H₄) |
| 2 | Ethene (C₂H₄) | Br₂ (addition), then alcoholic KOH ×2 (double dehydrohalogenation) | Ethyne (C₂H₂) |
| 3 | Ethyne (C₂H₂) | H₂O, Hg²⁺/H₂SO₄ (Markovnikov hydration) | Ethanal (CH₃CHO) |
🔄 Common Conversion Chains (Class XI-XII)
| Start | Reagent | End Product | Reaction Type |
|---|---|---|---|
| Alkyl Halide (R-X) | Alcoholic KOH | Alkene | Elimination (E2) |
| Alkene | HBr (Markovnikov) | Alkyl Halide | Electrophilic Addition |
| Alcohol (R-OH) | PCl₃ / SOCl₂ | Alkyl Halide | Substitution |
| Alcohol | Oxidation (K₂Cr₂O₄) | Aldehyde / Ketone | Oxidation |
| Aldehyde | Further Oxidation | Carboxylic Acid | Oxidation |
| Carboxylic Acid | Alcohol + H₂SO₄ (cat.) | Ester | Esterification |
| Aromatic Amine (Ar-NH₂) | NaNO₂ + HCl, 0-5°C | Diazonium Salt | Diazotization |
| Diazonium Salt | CuCl / CuBr / CuCN | Aryl Halide / Nitrile | Sandmeyer Reaction |
💡 How to Use This Map
Board exams frequently ask "convert X to Y in n steps" style questions. Practice tracing a path through this map from any starting compound to any target compound — identifying the correct reagent for each arrow is usually worth more marks than memorizing the final answer alone.
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