IMPORTANT NAME REACTION'S OF CSIR-NET, GATE, IIT-JEE & BARC EXAM
For any competitive Exam such as CSIR-NET, GATE, IIT-JEE, BARC & TIFR etc. The role of organic chemistry is very important compare to the others (e.g., Inorganic and physical). In Inorganic and Physical their is a chapter oriented question is asked but in organic chemistry there is no as such particular chapter basic questions. Actually all are combine to each other. So if you a good depth in simple general organic chemistry then you may answer easily any questions of organic portions.
Some important name reactions are given below which has been covered properly........
A
- Acyloin Condensation
- Aldol Condensation
- Alkyne Metathesis
- Appel Reaction
- Amadori Rearrangement
- Arndt-Eistert Synthesis
- Baeyer-Villiger Oxidation
- Bamford-Stevens Reaction
- Barton Reaction
- Beckmann Rearrangement
- Benzylic acid Rearrangement
- Benzoin Condensation
- Birch Reduction
- Bichler- Napierlaski Reactions
- Brook Rearrangement
- Bardhan-Sengupta Synthesis
- Benzoin Condentation
- Bouvault- Blanc Reduction
- Chugaev Ellimination
- Claisen Condensation
- Claisen Rearrangement
- Claisen-Scmidt Condentation
- Clemmensen Reduction
- Conrad- Limpach Synthesis
- Cope Ellimination
- Cope Rearrangement
- Corey-Fusch's Reaction
- Curtius Rearrangement
- Cannizaro Reaction
- Corey-House Synthesis
- Dakin Oxidation
- Dakin-West Reaction
- Darzens condensation
- Dess-Martin Oxidation
- Dieckmann Condensation
- Diels-Alder Reacion
- Doebner-Miler Condensation
- Demjanov Rearrangement
- Dienone-Phenol Rearrangement
- Ene Reaction
- Favourski Rearrangement
- Finkelstein Reaction
- Fischer-Indole Synthesis
- Fleming-Tamao Oxidation
- Friedel-Craft Acylation
- Friedel-Craft Alkylation
- Fries Rearrangement
- Fukuyama Indole Synthesis
- Gabriel Synthesis
- Gattermann & Gattermann-koch formylation
- Grignard Reaction
- Haloform Reaction
- Hantz dihydropyridine Synthesis
- Hell-Volhard-ZElinsky Reaction
- Hofmann Elimination
- Hofmann Rearrangement
- Houben-Hoesch Reaction
- Hunsdiecker Reaction
- Hofmann-Loffler-Fretag Reaction
- Jones Oxidation
- Julia Olifination
- Knoevenagel Condensation
- Knorr-Pyrrole Synthesis
- Kolbe-Schmitt reaction
- Kumada Coupling
- Lossen Rearrangement
- Malonic & Acetoacetic Ester Synthsis
- Manich Reaction
- Mcmurry REaction
- MPV Reduction
- Micheal Reaction
- Madelung indole Synthesis
- Mitsunobu Reaction
- Nef Reaction
- Negishi Coupling
- Norrish Reaction
- Oppenauer Oxidation
- Ozonolysis: Criegee Mechanism
- Orton Rearrangement
- Pall-Knorr furan Synthesis
- Pall-Knorr Pyrrole Synthesis
- Pall-Knorr Thiphene Synthesis
- Pechmann condensation : Coumarin synthesis
- Perkin Reaction
- Pinacol-pinacolon Rearrangement
- Peterson Olefination
- Pummere Rearrangement
R
- Reformatsky Reaction
- Reimer-Tiemann Reaction
- Robinson annulation
- Rosenmund Reduction
- Rupe Rearrangement
- Sandmayer Reaction
- Scmidt Rearrangement
- Schotten-Baumann Reaction
- Shapiro Reaction
- Sharpless Asymmetric Epoxidation
- Simmons-Smith Reaction
- Skraup & Doebner-Miller quinoline Synthesis
- Sommlet Reaction
- Stephen aldehyde Synthesis
- Stobbe Condensation
- Stork Enamine Synthesis
- Streeker Synthesis
- Swern Oxidation
- Sharpless Asymmetric Dihydrolylation
- SEmi-Pinacol Rearrangement
- Suzuki Coupling
- Stille Coupling
- Sonogashira Coupling
- Studinger Reaction
- Tichenko Reaction
- Tiffeneav-Demjanov Rearrangement
- Ullmann-biaryl Synthesis
- Vilsmeirer-Haack Reaction
- Von-pechmann Reaction
- Von-Richter Rearrangement
- Wagner-Meerwein Rearrangement
- Willamson-Ether Synthesis
- Wittig Reaction
- Wohl-Ziegler Reaction
- Wolf-Krishner Reduction
- Wurtz Reaction
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