#1
12th July 2016, 05:46 PM
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Named Reactions in Organic Chemistry for IIT JEE
Can you list me the name of Organic Chemistry Reactions that are important for preparation Indian Institutes of Technology Joint Entrance Examination (IIT-JEE)?
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#2
12th July 2016, 06:23 PM
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Re: Named Reactions in Organic Chemistry for IIT JEE
The name of Organic Chemistry Reactions that are important for preparation Indian Institutes of Technology Joint Entrance Examination (IIT-JEE) are as follows: Acetoacetic Ester Condensation Acetoacetic Ester Synthesis Acyloin Condensation Alder-Ene Reaction Aldol Addition Aldol Condensation Appel Reaction Arbuzov Reaction Arndt-Eistert Synthesis Azide-Alkyne 1, 3-Dipolar Cycloaddition Azo Coupling Baeyer-Villiger Oxidation Baker-Venkataraman Rearrangement Balz-Schiemann Reaction Bamford-Stevens Reaction Barton Decarboxylation Barton-McCombie Reaction (Barton Desoxygenation) Baylis-Hillman Reaction Beckmann Rearrangement Benzilic Acid Rearrangement Benzoin Condensation Bergman Cyclization Bestmann-Ohira Reagent Biginelli Reaction Birch Reduction Bischler-Napieralski Reaction Blaise Reaction Blanc Reaction Bohlmann-Rahtz Pyridine Synthesis Boronic Acid Mannich Reaction Bouveault-Blanc Reduction Brook Rearrangement Brown Hydroboration Bucherer-Bergs Reaction Buchwald-Hartwig Cross Coupling Reaction Cadiot-Chodkiewicz Coupling Cannizzaro Oxidation Reduction CBS Reduction Chan-Lam Coupling Claisen Condensation Claisen Rearrangement Clemmensen Reduction Click Chemistry Collins Reagent Conia-Ene Reaction Cope Elimination Cope Rearrangement Corey-Bakshi-Shibata Reduction Corey-Chaykovsky Reaction Corey-Fuchs Reaction Corey-Kim Oxidation Corey-Seebach Reaction Corey-Suggs Reagent Corey-Winter Olefin Synthesis Coumarin Synthesis Criegee Mechanism for Ozonolysis Cross Metathesis Curtius Rearrangement (Reaction) Dakin Reaction Darzens Condensation Darzens Reaction De Kimpe Aziridine Synthesis Delépine Reaction Dess-Martin Oxidation Diazotisation Dieckmann Condensation Diels-Alder Reaction Directed ortho Metalation Doebner Modification Eglinton Reaction Ene Reaction Enyne Metathesis Epoxidation Eschweiler-Clarke Reaction Ester Pyrolysis Esterification Favorskii Reaction Finkelstein Reaction Fischer Esterification Fischer Indole Synthesis Fleming-Tamao Oxidation Friedel-Crafts Acylation Friedel-Crafts Alkylation Friedlaender Synthesis Fries Rearrangement Fukuyama Coupling Fukuyama Reduction Gabriel Synthesis Gewald Reaction Glaser Coupling Griesbaum Coozonolysis Grignard Reaction Grubbs Reaction Haloform Reaction Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis) Hay Coupling Heck Reaction Hell-Volhard-Zelinsky Reaction Henry Reaction Hiyama Coupling Hiyama-Denmark Coupling Hofmann Elimination Hofmann's Rule Horner-Wadsworth-Emmons Reaction Hosomi-Sakurai Reaction Huisgen Cycloaddition Hunsdiecker Reaction Hydroboration Ireland-Claisen Rearrangement Itsuno-Corey Reduction Iwanow Reaction (Reagent) Jacobsen Epoxidation Jacobsen-Katsuki Epoxidation Jocic Reaction Johnson-Corey-Chaykovsky Reaction Jones Oxidation Julia-Kocienski Olefination Julia-Lythgoe Olefination Kabachnik-Fields Reaction Kindler Reaction Knoevenagel Condensation Kochi Reaction Kolbe Electrolysis Kolbe Nitrile Synthesis Kolbe-Schmitt Reaction Koser's Reagent Kulinkovich Reaction Kulinkovich-de Meijere Reaction Kulinkovich-Szymoniak Reaction Kumada Coupling Lawesson's Reagent Leuckart Thiophenol Reaction Luche Reduction Malonic Ester Synthesis Mannich Reaction Markovnikov's Rule McMurry Reaction Meerwein-Ponndorf-Verley Reduction Michael Addition Michaelis-Arbuzov Reaction Mitsunobu Reaction Miyaura Borylation Reaction Modified Julia Olefination Mukaiyama Aldol Addition Myers' Modification of the Ramberg-Bäcklund Reaction Myers-Saito Cyclization Nazarov Cyclization Nef Reaction Negishi Coupling Newman-Kwart Rearrangement Nitroaldol Reaction Nozaki-Hiyama Coupling Nucleophilic Substitution (SN1 / SN2) Ohira-Bestmann Reagent Olefin Metathesis Oppenauer Oxidation Overman Rearrangement Oxy-Cope Rearrangement Ozonolysis Paal-Knorr Furan Synthesis Paal-Knorr Pyrrole Synthesis Paal-Knorr Thiophene Synthesis Passerini Reaction Paterno-Büchi Reaction Pauson-Khand Reaction Pechmann Condensation Petasis Reaction Peterson Olefination Pinacol Coupling Reaction Pinacol Rearrangement Pinner Reaction Prévost Reaction Prilezhaev Reaction Prins Reaction Pschorr Reaction Ramberg-Bäcklund Reaction Reformatsky Reaction Ring Closing Metathesis Ring Opening Metathesis (Polymerization) Ritter Reaction Robinson Annulation Rosenmund Reduction Rosenmund-von Braun Reaction Rubottom Oxidation Sakurai Reaction Sandmeyer Reaction Sarett Reagent Saytzeff's Rule Schiemann Reaction Schlosser Modification Schmidt Reaction Schotten-Baumann Reaction Seebach Umpolung Seyferth-Gilbert Homologation Shapiro Reaction Sharpless Aminohydroxylation Sharpless Dihydroxylation Sharpless Epoxidation Shi Epoxidation Simmons-Smith Reaction Sonogashira Coupling Staudinger Cycloaddition Staudinger Reaction Staudinger Reduction Staudinger Synthesis Steglich Esterification Stetter Reaction Stille Coupling Strecker Synthesis Suzuki Coupling Swern Oxidation Tamao-Kumada Oxidation Tebbe Olefination Tishchenko Reaction Trost Allylation Tsuji-Trost Reaction Ugi Reaction Ullmann Reaction Upjohn Dihydroxylation Van Leusen Imidazole Synthesis Van Leusen Oxazole Synthesis Van Leusen Reaction Vicarious Nucleophilic Substitution Vilsmeier Reaction Wacker-Tsuji Oxidation Weinreb Ketone Synthesis Wenker Synthesis Willgerodt-Kindler Reaction Williamson Synthesis Wittig Reaction Wittig-Horner Reaction Wohl-Ziegler Reaction Wolff Rearrangement Wolff-Kishner Reduction Woodward Reaction Woodward cis-Hydroxylation Wurtz Reaction Wurtz-Fittig Reaction Yamaguchi Esterification |
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