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   
B
  • 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
C
  • 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
D
  • Dakin Oxidation
  • Dakin-West Reaction
  • Darzens condensation
  • Dess-Martin Oxidation
  • Dieckmann Condensation
  • Diels-Alder Reacion
  • Doebner-Miler Condensation
  • Demjanov  Rearrangement
  • Dienone-Phenol  Rearrangement
E
  • Ene Reaction
F
  • Favourski Rearrangement
  • Finkelstein Reaction
  • Fischer-Indole Synthesis
  • Fleming-Tamao Oxidation
  • Friedel-Craft Acylation
  • Friedel-Craft Alkylation
  • Fries Rearrangement
  • Fukuyama Indole Synthesis
G
  • Gabriel Synthesis
  • Gattermann & Gattermann-koch formylation
  • Grignard Reaction
H
  • Haloform Reaction
  • Hantz dihydropyridine Synthesis
  • Hell-Volhard-ZElinsky Reaction
  • Hofmann Elimination
  • Hofmann Rearrangement
  • Houben-Hoesch Reaction
  • Hunsdiecker Reaction
  • Hofmann-Loffler-Fretag Reaction
J
  • Jones Oxidation
  • Julia Olifination
K
  • Knoevenagel Condensation
  • Knorr-Pyrrole Synthesis
  • Kolbe-Schmitt reaction
  • Kumada Coupling
L
  • Lossen Rearrangement
M
  • Malonic & Acetoacetic Ester Synthsis
  • Manich Reaction
  • Mcmurry REaction
  • MPV Reduction
  • Micheal Reaction
  • Madelung indole Synthesis
  • Mitsunobu Reaction
N
  • Nef Reaction
  • Negishi Coupling
  • Norrish Reaction
O
  • Oppenauer Oxidation
  • Ozonolysis: Criegee Mechanism
  • Orton Rearrangement
P
  • 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
S
  • 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
T
  • Tichenko Reaction
  • Tiffeneav-Demjanov Rearrangement
U
  • Ullmann-biaryl Synthesis
V
  • Vilsmeirer-Haack Reaction
  • Von-pechmann Reaction
  • Von-Richter Rearrangement
W
  • Wagner-Meerwein Rearrangement
  • Willamson-Ether Synthesis
  • Wittig Reaction
  • Wohl-Ziegler Reaction 
  • Wolf-Krishner Reduction
  • Wurtz Reaction


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