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List of all reactions in organic chemistry

List of all reactions in organic chemistry


3 Answers

18 Points
7 years ago
Heres an entire list But learning all this is too much A Abramovitch–Shapiro tryptamine synthesis Acetalisation Acetoacetic ester condensation Achmatowicz reaction Acylation Acyloin condensation Adams catalyst Adams decarboxylation Adkins catalyst Adkins–Peterson reaction Akabori amino acid reaction Alcohol oxidation Alder ene reaction Alder–Stein rules Aldol addition Aldol condensation Algar–Flynn–Oyamada reaction Alkylimino-de-oxo-bisubstitution Alkyne trimerisation Alkyne zipper reaction Allan–Robinson reaction Allylic rearrangement Amadori rearrangement Amine alkylation Angeli–Rimini reaction Andrussov oxidation Appel reaction Arbuzov reaction, Arbusow reaction Arens–van Dorp synthesis, Isler modification Aromatic nitration Arndt–Eistert synthesis Auwers synthesis Azo coupling B Baeyer–Drewson indigo synthesis Baeyer–Villiger oxidation Baeyer–Villiger rearrangement Bakeland process (Bakelite) Baker–Venkataraman rearrangement, Baker–Venkataraman transformation Bally–Scholl synthesis Balz–Schiemann reaction Bamberger rearrangement Bamberger triazine synthesis Bamford–Stevens reaction Barbier–Wieland degradation Bardhan–Sengupta phenanthrene synthesis Barfoed`s test Bartoli indole synthesis, Bartoli reaction Barton reaction Barton–Kellogg reaction Barton–McCombie reaction, Barton deoxygenation Barton Zard Synthesis Barton vinyl iodine procedure Baudisch reaction Bayer test Baylis–Hillman reaction Bechamp reaction Bechamp reduction Beckmann fragmentation Beckmann rearrangement Bellus–Claisen rearrangement Belousov–Zhabotinsky reaction Benary reaction Benedict`s reagent Benkeser reaction Benzidine rearrangement Benzilic acid rearrangement Benzoin condensation Bergman cyclization Bergmann azlactone peptide synthesis Bergmann degradation Bergmann–Zervas carbobenzoxy method Bernthsen acridine synthesis Bestmann`s reagent Betti reaction Biginelli pyrimidine synthesis Biginelli reaction Bingel reaction Birch reduction Bischler–Möhlau indole synthesis Bischler–Napieralski reaction Biuret test Blaise ketone synthesis Blaise reaction Blanc reaction Blanc chloromethylation Bodroux reaction Bodroux–Chichibabin aldehyde synthesis Bogert–Cook synthesis Bohn–Schmidt reaction Boord olefin synthesis Borodin reaction Borsche–Drechsel cyclization Bosch–Meiser urea process Bouveault aldehyde synthesis Bouveault–Blanc reduction Boyland–Sims oxidation Boyer Reaction Bredt`s rule Brown hydroboration Bucherer carbazole synthesis Bucherer reaction Bucherer–Bergs reaction Buchner ring enlargement Büchner–Curtius–Schlotterbeck reaction Buchwald–Hartwig amination Bunnett reaction C Cadiot–Chodkiewicz coupling Camps quinoline synthesis Cannizzaro reaction Carbohydrate acetalisation Carbonyl reduction Carbonylation Carbylamine reaction Carroll reaction Castro–Stephens coupling Catalytic reforming Catellani Reaction CBS reduction Chan–Lam coupling Chapman rearrangement Cheletropic reaction Chichibabin pyridine synthesis Chichibabin reaction Chiral pool synthesis Chugaev elimination Ciamician–Dennstedt rearrangement Claisen condensation Claisen rearrangement Claisen–Schmidt condensation Clemmensen reduction Collins reagent Combes quinoline synthesis Conia reaction Conrad–Limpach synthesis Corey–Gilman–Ganem oxidation Cook–Heilbron thiazole synthesis Cope elimination Cope rearrangement Corey reagent Corey–Bakshi–Shibata reduction Corey–Fuchs reaction Corey–Kim oxidation Corey–Posner, Whitesides–House reaction Corey–Winter olefin synthesis Corey–Winter reaction Coupling reaction Craig method Cram`s rule of asymmetric induction Creighton process Criegee reaction Criegee rearrangement Cross metathesis Crum Brown–Gibson rule Curtius degradation Curtius rearrangement, Curtius reaction Cyanohydrin reaction Dakin reaction Dakin–West reaction Danheiser Annulation Darapsky degradation Darzens condensation, Darzens–Claisen reaction, Glycidic ester condensation Darzens synthesis of unsaturated ketones Darzens tetralin synthesis Dehydration reaction Dehydrogenation Delepine reaction Demjanov rearrangement Demjanow desamination Dess–Martin oxidation Diazoalkane 1,3-dipolar cycloaddition Diazotisation DIBAL-H selective reduction Dieckmann condensation Dieckmann reaction Diels–Alder reaction Diels–Reese reaction Dienol benzene rearrangement Dienone phenol rearrangement Dimroth rearrangement Di-pi-methane rearrangement Directed ortho metalation Doebner modification Doebner reaction Doebner–Miller reaction, Beyer method for quinolines Doering–LaFlamme carbon chain extension Dötz reaction Dowd–Beckwith ring expansion reaction Duff reaction Dutt–Wormall reaction Dyotropic reaction E1cB elimination reaction Eder reaction Edman degradation Eglinton reaction Ehrlich–Sachs reaction Einhorn variant Einhorn–Brunner reaction Elbs persulfate oxidation Elbs reaction Electrochemical fluorination Electrocyclic reaction Electrophilic halogenation Electrophilic amination Elimination reaction Emde degradation Emmert reaction Ene reaction Enyne metathesis Epoxidation Erlenmeyer synthesis, Azlactone synthesis Erlenmeyer–Plöchl azlactone and amino-acid synthesis Eschenmoser fragmentation Eschweiler–Clarke reaction Ester pyrolysis Ether cleavage Étard reaction Evans aldol Favorskii reaction Favorskii rearrangement Favorskii–Babayan synthesis Fehling test Feist–Benary synthesis Fenton reaction Ferrario reaction Ferrier carbocyclization Ferrier rearrangement Finkelstein reaction Fischer indole synthesis Fischer oxazole synthesis Fischer peptide synthesis Fischer phenylhydrazine and oxazone reaction Fischer glycosidation Fischer–Hepp rearrangement Fischer–Speier esterification Fischer Tropsch synthesis Fleming–Tamao oxidation Flood reaction Folin–Ciocalteu reagent Formox process Forster reaction Forster–Decker method Fowler process Franchimont reaction Frankland synthesis Frankland–Duppa reaction Free radical halogenation Freund reaction Friedel–Crafts acylation Friedel–Crafts alkylation Friedländer synthesis Fries rearrangement Fritsch–Buttenberg–Wiechell rearrangement Fujimoto–Belleau reaction Fukuyama coupling Fukuyama indole synthesis Fukuyama reduction Gabriel ethylenimine method Gabriel synthesis Gabriel–Colman rearrangement, Gabriel isoquinoline synthesis Gallagher–Hollander degradation Gassman indole synthesis Gastaldi synthesis Gattermann aldehyde synthesis Gattermann Koch reaction Gattermann reaction Geminal halide hydrolysis Gewald reaction Gibbs phthalic anhydride process Gilman reagent Glaser coupling Glycol cleavage Gomberg–Bachmann reaction Gomberg–Bachmann–Hey reaction Gomberg free-radical reaction Gould–Jacobs reaction Graebe–Ullmann synthesis Grignard degradation Grignard reaction Grob fragmentation Groove synthesis Grubbs` catalyst in Olefin metathesis Grundmann aldehyde synthesis Gryszkiewicz–Trochimowski and McCombie method Guareschi–Thorpe condensation Guerbet reaction Gutknecht pyrazine synthesis Haber–Weiss reaction Haller–Bauer reaction Haloform reaction Halogen addition reaction Halohydrin formation reaction Hammett equation Hammick reaction Hammond principle or Hammond postulate Hantzsch pyrrole synthesis Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis Hantzsch pyridine synthesis, Gattermann–Skita synthesis, Guareschi–Thorpe condensation, Knoevenagel–Fries modification Hantzsch–Collidin synthesis Harries ozonide reaction Haworth methylation Haworth Phenanthrene synthesis Haworth reaction Hay coupling Hayashi rearrangement Heck reaction Helferich method Hell–Volhard–Zelinsky halogenation Hemetsberger indole synthesis Hemetsberger–Knittel synthesis Henkel reaction, Raecke process, Henkel process Henry reaction, Kamlet reaction Herz reaction, Herz compounds Herzig–Meyer alkimide group determination Heumann indigo synthesis Hydration reaction Hydroamination Hydrodesulfurization Hydrogenolysis Hydrosilylation Hinsberg indole synthesis Hinsberg oxindole synthesis Hinsberg reaction Hinsberg separation Hinsberg sulfone synthesis Hoch–Campbell ethylenimine synthesis Hock rearrangement Hofmann degradation, Exhaustive methylation Hofmann elimination Hofmann Isonitrile synthesis, Carbylamine reaction Hofmann produkt Hofmann rearrangement Hofmann–Löffler reaction, Löffler–Freytag reaction, Hofmann–Löffler–Freytag reaction Hofmann–Martius rearrangement Hofmann`s rule Hofmann–Sand reaction Homo rearrangement of steroids Hooker reaction Horner–Wadsworth–Emmons reaction Hoesch reaction Hosomi–Sakurai reaction Houben–Fischer synthesis Hudlicky fluorination Hunsdiecker reaction Hydroboration Hydrocarbon cracking Hydrohalogenation Indium mediated allylation Ing–Manske procedure Ipso substitution Ishikawa reagent trans-cis isomerism Ivanov reagent, Ivanov reaction Jacobsen epoxidation Jacobsen rearrangement Janovsky reaction Japp–Klingemann reaction Japp–Maitland condensation Johnson–Claisen rearrangement Jones oxidation Jordan–Ullmann–Goldberg synthesis Julia olefination Julia–Lythgoe olefination Kabachnik–Fields reaction Kharasch–Sosnovsky reaction Ketone halogenation Kiliani–Fischer synthesis Kindler reaction Kishner cyclopropane synthesis Knoevenagel condensation Knorr pyrazole synthesis Knorr pyrrole synthesis Knorr quinoline synthesis Koch–Haaf reaction Kochi reaction Koenigs–Knorr reaction Kolbe electrolysis Kolbe–Schmitt reaction König method Kornblum oxidation Kornblum–DeLaMare rearrangement Kostanecki acylation Kowalski ester homologation Krapcho decarboxylation Kröhnke aldehyde synthesis Kröhnke oxidation Kröhnke pyridine synthesis Kucherov reaction Kuhn–Winterstein reaction Kulinkovich reaction Kumada coupling Larock indole synthesis Lebedev process Lehmstedt–Tanasescu reaction Leimgruber–Batcho indole synthesis Letts nitrile synthesis Leuckart reaction Leuckart thiophenol reaction Leuckart–Wallach reaction Leuckart amide synthesis Levinstein process Ley oxidation Lieben iodoform reaction, Haloform reaction Liebeskind–Srogl coupling Liebig melamine synthesis Lindlar catalyst Lobry–de Bruyn–van Ekenstein transformation Lossen rearrangement Lucas` reagent Luche reduction Maillard reaction Madelung synthesis Malaprade reaction, Periodic acid oxidation Malonic ester synthesis Mannich reaction Markó–Lam deoxygenation Markovnikov`s rule, Markownikoff rule, Markownikow rule Martinet dioxindole synthesis McDougall monoprotection McFadyen–Stevens reaction McMurry reaction Meerwein arylation Meerwein–Ponndorf–Verley reduction Meisenheimer rearrangement Meissenheimer complex Menshutkin reaction Metal-ion-catalyzed s-bond rearrangement Mesylation Merckwald asymmetric synthesis Methylation Meyer and Hartmann reaction Meyer reaction Meyer synthesis Meyer–Schuster rearrangement Michael addition Michael addition, Michael system Michael condensation Michaelis–Arbuzov reaction Mignonac reaction Milas hydroxylation of olefins Mitsunobu reaction Molisch`s test Mukaiyama aldol addition Mukaiyama reaction Myers` asymmetric alkylation Nametkin rearrangement Nazarov cyclization reaction Neber rearrangement Nef reaction Negishi coupling Negishi zipper reaction Nenitzescu indole synthesis Nenitzescu reductive acylation Nicholas reaction Niementowski quinazoline synthesis Niementowski quinoline synthesis Nierenstein reaction NIH shift Ninhydrin test Nitroaldol reaction Nitrone-olefin 3+2 cycloaddition Normant reagents Noyori asymmetric hydrogenation Nozaki–Hiyama–Kishi reaction Nucleophilic acyl substitution Ohira–Bestmann reaction Olah reagent Olefin metathesis Oppenauer oxidation Ostromyslenskii reaction, Ostromisslenskii reaction Oxidative decarboxylation Oxo synthesis Oxy-Cope rearrangement Oxymercuration Oxidation of secondary alcohols to ketones Ozonolysis Paal–Knorr pyrrole synthesis Paal–Knorr synthesis Paneth technique Passerini reaction Paternò–Büchi reaction Pauson–Khand reaction Payne rearrangement Pechmann condensation Pechmann pyrazole synthesis Pellizzari reaction Pelouze synthesis Peptide synthesis Perkin alicyclic synthesis Perkin reaction Perkin rearrangement Perkow reaction Petasis reaction Petasis reagent Peterson olefination Peterson reaction Petrenko-Kritschenko piperidone synthesis Pfau–Plattner azulene synthesis Pfitzinger reaction Pfitzner–Moffatt oxidation Piancatelli rearrangement Pictet–Gams isoquinoline synthesis Pictet–Hubert reaction Pictet–Spengler tetrahydroisoquinoline synthesis Pictet–Spengler reaction Piloty–Robinson pyrrole synthesis Pinacol coupling reaction Pinacol rearrangement Pinner amidine synthesis Pinner method for ortho esters Pinner reaction Pinner triazine synthesis Piria reaction Pitzer strain Polonovski reaction Pomeranz–Fritsch reaction Ponzio reaction Prato reaction Prelog strain Prevost reaction Prileschajew reaction Prilezhaev reaction Prins reaction Prinzbach synthesis Protecting group Pschorr reaction Pummerer rearrangement Purdie methylation, Irvine–Purdie methylation Quelet reaction Ramberg–Bäcklund reaction Raney nickel Rap–Stoermer condensation Raschig phenol process Rauhut–Currier reaction Racemization Reductive amination Reductive dehalogenation of halo ketones Reed reaction Reformatskii reaction Reilly–Hickinbottom rearrangement Reimer–Tiemann reaction Reissert indole synthesis Reissert reaction, Reissert compound Reppe synthesis Retropinacol rearrangement Rieche formylation Riemschneider thiocarbamate synthesis Riley oxidations Rothemund synthesis Ring closing metathesis Ring opening metathesis Ritter reaction Robinson annulation Robinson–Gabriel synthesis Robinson Schopf reaction Rosenmund reaction Rosenmund reduction Rosenmund–von Braun synthesis Rothemund reaction Rupe rearrangement Rubottom oxidation Ruff–Fenton degradation Ruzicka large-ring synthesis Sakurai reaction Salol reaction Sandheimer Sandmeyer diphenylurea isatin synthesis Sandmeyer isonitrosoacetanilide isatin synthesis Sandmeyer reaction Sanger reagent Saponification Sarett oxidation Saytzeff rule, Saytzeff`s Rule Schiemann reaction Schiff reaction Schiff test Schlenk equilibrium Schlosser modification Schlosser variant Schmidlin ketene synthesis Schmidt degradation Schmidt reaction Scholl reaction Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction Schotten–Baumann reaction Seliwanoff`s test Semidine rearrangement Semmler–Wolff reaction Seyferth–Gilbert homologation Shapiro reaction Sharpless asymmetric dihydroxylation Sharpless epoxidation Sharpless oxyamination or aminohydroxylation Shenck ene reaction Sigmatropic reaction Simmons–Smith reaction Simonini reaction Simonis chromone cyclization Simons process Skraup chinolin synthesis Skraup reaction Smiles rearrangement SNAr nucleophilic aromatic substitution SN1 SN2 SNi Solvolysis Sommelet reaction Sonn–Müller method Sonogashira coupling Sørensen formol titration Staedel–Rugheimer pyrazine synthesis Staudinger reaction Stephen aldehyde synthesis Stetter reaction Stevens rearrangement Stieglitz rearrangement Stille coupling Stobbe condensation Stollé synthesis Stork acylation Stork enamine alkylation Strecker amino acid synthesis Strecker degradation Strecker sulfite alkylation Strecker synthesis Suzuki coupling Swain equation Swarts reaction Swern oxidation Tamao oxidation Tafel rearrangement Takai olefination Tebbe olefination ter Meer reaction Thiele reaction Thiol-yne reaction Thorpe reaction Tiemann rearrangement Tiffeneau ring enlargement reaction Tiffeneau–Demjanov rearrangement Tischtschenko reaction Tishchenko reaction, Tishchenko–Claisen reaction Tollens reagent Transfer hydrogenation Trapp mixture Transesterification Traube purine synthesis Truce–Smiles rearrangement Tscherniac–Einhorn reaction Tschitschibabin reaction Tschugajeff reaction Twitchell process Tyrer sulfonation process Ugi reaction Ullmann reaction Upjohn dihydroxylation Urech cyanohydrin method Urech hydantoin synthesis Van Slyke determination Varrentrapp reaction Vilsmeier reaction Vilsmeier–Haack reaction Voight amination Volhard–Erdmann cyclization von Braun amide degradation von Braun reaction von Richter cinnoline synthesis von Richter reaction Wacker–Tsuji oxidation Wagner-Jauregg reaction Wagner–Meerwein rearrangement Waits–Scheffer epoxidation Walden inversion Wallach rearrangement Weerman degradation Weinreb ketone synthesis Wenker ring closure Wenker synthesis Wessely–Moser rearrangement Westphalen–Lettré rearrangement Wharton reaction Whiting reaction Wichterle reaction Widman–Stoermer synthesis Wilkinson catalyst Willgerodt rearrangement Willgerodt–Kindler reaction Williamson ether synthesis Winstein reaction Wittig reaction Wittig rearrangement Wittig–Horner reaction Wohl degradation Wohl–Aue reaction Wohler synthesis Wohl–Ziegler reaction Wolffenstein–Böters reaction Wolff rearrangement Wolff–Kishner reduction Woodward cis-hydroxylation Woodward–Hoffmann rule Wulff–Dötz reaction Wurtz coupling, Wurtz reaction Wurtz–Fittig reaction Yamada–Okamoto purine synthesis Yamaguchi esterification Zeisel determination Zerevitinov determination, Zerewitinoff determination Ziegler condensation Ziegler method Zimmermann reaction Zincke disulfide cleavage Zinke nitration Zincke reaction Zincke–Suhl reaction Zinin reduction
ruchi yadav
askIITians Faculty 27 Points
7 years ago
Brown Hydroboration, Carbylamine Reaction (Isocyanide Test), Cannizzaro Reaction, Clemmensen Reduction, Coupling Reaction, Rosenmunds Reaction, Riemer-Tiemann Reaction, Fries Rearrangement, Friedel-Crafts Acylation Reaction, Gabriel Phthalimide Reaction, Hinsbergs Test, Hoffmann Bromamide Reaction, Sandmeyers Reaction, Diazotization.

Thank You,
Askiitian's Faculty

ruchi yadav
askIITians Faculty 27 Points
7 years ago
Name reactions -Brown Hydroboration, Carbylamine Reaction (Isocyanide Test), Cannizzaro Reaction, Clemmensen Reduction, Coupling Reaction, Rosenmunds Reaction, Riemer-Tiemann Reaction, Fries Rearrangement, Friedel-Crafts Acylation Reaction, Gabriel Phthalimide Reaction, Hinsbergs Test, Hoffmann Bromamide Reaction, Sandmeyers Reaction, Diazotization.

Thank You
Askiitians Faculty

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