03 WEEKS
Rapidiously develop parallel e-markets via worldwide paradigms. Quickly synergize cutting-edge scenarios and professional results. Assertively deliver cross-media results before client-centric results. Uniquely initiate intuitive communities through process-centric internal or "organic" sources. Energistically reinvent distinctive value via parallel services. Phosfluorescently deploy extensive paradigms vis-a-vis cross-unit manufactured products. Uniquely coordinate impactful services whereas team building e-services. Globally grow multimedia based benefits vis-a-vis client-based niches.
| Day | Topics Covered |
|---|---|
| Day 1 | Basic of organic chemistry like reaction graph intermediate, electrophile, nucleophile, acidic or basic medium |
| Day 2 | Link between reaction and intermediate and their stability, Kinetics vs Thermodynamics |
| Day 3 | How reaction proceeds in basic or acidic medium—Enolate reaction |
| Day 4 | Nucleophile vs Basic medium and difference with reactions and name reaction: Electrophilic substitution reaction, Sandmeyer reaction, Gattermann-Koch reaction, Stephen reaction |
| Day 5 | Nucleophile vs Electrophile and their mechanism, Oxidation, Reduction (CrO3) |
| Day 6 | Reaction of hydrocarbons: Birch reduction, Ozonolysis, Grignard reaction, Corey-House reaction |
| Day 7 | Reaction of alkyl halide: Wurtz reaction, Wurtz-Fittig reaction, reaction with metals (Frankland reaction), Grignard reaction, Friedel-Crafts reaction, reaction of Grignard with carbonyl to give 1°, 2°, 3° alcohols, reaction with ester, reaction with anhydride, reaction with O2, CN |
| Day 8 | Reaction of carbonyl: From Grignard, hydroboration, Stephen method, Rosenmund reaction, reaction with hydroxylamine, hydrazine, phenylhydrazine, 2,4-Dinitrophenylhydrazine, Semicarbazide, Aldol reaction, Perkin condensation, Baeyer-Villiger oxidation, Clemmensen reduction, Wolff-Kishner reduction, Cannizzaro reaction, Wittig reaction, Reformatsky reaction |
| Day 9 | Reaction of carboxylic acid: Hell-Volhard-Zelinsky Reaction, Kolbe electrolytic synthesis, esterification, LiAlH4 |
| Day 10 | Amines: Gabriel phthalimide synthesis, Hoffmann bromamide degradation reaction, Lossen rearrangement, Beckmann rearrangement, Fritsch-Buttenberg-Wiechell rearrangement |
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| Day | Topics Covered |
|---|---|
| Day 1 | Basic of organic chemistry like reaction graph intermediate, electrophile, nucleophile, acidic or basic medium |
| Day 2 | Link between reaction and intermediate and their stability, Kinetics vs Thermodynamics |
| Day 3 | How reaction proceeds in basic or acidic medium—Enolate reaction |
| Day 4 | Nucleophile vs Basic medium and difference with reactions and name reaction: Electrophilic substitution reaction, Sandmeyer reaction, Gattermann-Koch reaction, Stephen reaction |
| Day 5 | Nucleophile vs Electrophile and their mechanism, Oxidation, Reduction (CrO3) |
| Day 6 | Reaction of hydrocarbons: Birch reduction, Ozonolysis, Grignard reaction, Corey-House reaction |
| Day 7 | Reaction of alkyl halide: Wurtz reaction, Wurtz-Fittig reaction, reaction with metals (Frankland reaction), Grignard reaction, Friedel-Crafts reaction, reaction of Grignard with carbonyl to give 1°, 2°, 3° alcohols, reaction with ester, reaction with anhydride, reaction with O2, CN |
| Day 8 | Reaction of carbonyl: From Grignard, hydroboration, Stephen method, Rosenmund reaction, reaction with hydroxylamine, hydrazine, phenylhydrazine, 2,4-Dinitrophenylhydrazine, Semicarbazide, Aldol reaction, Perkin condensation, Baeyer-Villiger oxidation, Clemmensen reduction, Wolff-Kishner reduction, Cannizzaro reaction, Wittig reaction, Reformatsky reaction |
| Day 9 | Reaction of carboxylic acid: Hell-Volhard-Zelinsky Reaction, Kolbe electrolytic synthesis, esterification, LiAlH4 |
| Day 10 | Amines: Gabriel phthalimide synthesis, Hoffmann bromamide degradation reaction, Lossen rearrangement, Beckmann rearrangement, Fritsch-Buttenberg-Wiechell rearrangement |
