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Chemical Reactions

A chemical reaction is a process that leads to the conversion of one type of chemical substances to another. Chemical reactions can be either spontaneous which means requiring no contribution of energy, or non-spontaneous which means typically following the input of some kind of energy, like heat, electricity or light. Typically, chemical reactions include changes that strictly include the motion of electrons in forming and breaking of chemical bonds among atoms, and can sometimes be explained by a chemical equation.

The common concept of chemical reactions between atoms has been expanded to the non-chemical reactions among entities smaller than atoms, involving radioactive decays, nuclear reactions, and reactions between elementary particles as explained by quantum field theory.

1,2-Wittig rearrangement 1,3-Dipolar cycloaddition reaction
Acetalisation of Carbonyls Achmatowicz reaction
Acylation Acyloin condensation
Adams catalyst Adams Decarboxylation
Adkins–Peterson reaction Akabori amino-acid reaction
Alcohol oxidation Alder Ene reaction
Aldol condensation Aldol reaction
Aldol-Tishchenko reaction Algar–Flynn–Oyamada reaction
Alkylimino-de-oxo-bisubstitution Alkyne trimerisation
Alkyne zipper reaction Allan–Robinson reaction
Allylic rearrangement Amadori rearrangement
Amine alkylation Andrussow process
Angeli–Rimini reaction Anthraquinone
Appel reaction Arndt–Eistert reaction
Aromatic sulfonation Azo coupling
Baeyer's Reagent Baeyer–Drewson indigo synthesis
Baeyer–Villiger oxidation Baker–Venkataraman rearrangement
Balz–Schiemann reaction Bamberger rearrangement
Bamberger triazine synthesis Bamford–Stevens reaction
Barfoed's test Bartoli indole synthesis
Barton reaction Barton–Kellogg reaction
Barton–McCombie deoxygenation Barton–Zard synthesis
Baudisch reaction Baylis–Hillman reaction
Bechamp reaction Bechamp reduction
Beckmann rearrangement Benary reaction
Benkeser reaction Benzilic acid rearrangement
Benzoin condensation Bergman cyclization
Bergmann degradation Bernthsen acridine synthesis
Betti reaction Biginelli reaction
Birch Reduction Bischler–Mohlau indole synthesis
Bischler–Napieralski reaction Blaise ketone synthesis
Blaise reaction Blanc chloromethylation
Bodroux–Chichibabin aldehyde synthesis Boord olefin synthesis
Bouveault aldehyde synthesis Bouveault–Blanc reduction
Boyland–Sims oxidation Bucherer carbazole synthesis
Bucherer reaction Bucherer–Bergs reaction
Buchwald–Hartwig amination Cadiot-Chodkiewicz coupling
Cadiot–Chodkiewicz coupling Camps quinoline synthesis
Cannizzaro reaction Carbohydrate acetalisation
Carbylamine reaction Carroll rearrangement
Castro–Stephens coupling CBS catalyst
Chichibabin pyridine synthesis Chichibabin reaction
Chugaev elimination Claisen condensation
Claisen rearrangement Clemmensen reduction
Collins reagent Combes quinoline synthesis
Conrad–Limpach synthesis Cook–Heilbron thiazole synthesis
Cope reaction Cope rearrangement
Corey–Fuchs reaction Corey–House synthesis
Corey–Itsuno reduction Corey–Kim oxidation
Corey–Winter olefin synthesis Creighton process
Criegee rearrangement Cumene process
Curtius rearrangement Cyanohydrin reaction
Dakin oxidation Dakin–West reaction
Danheiser annulation Darzens reaction
Darzens tetralin synthesis Dehydrogenation
Delepine reaction Demjanov rearrangement
Dess–Martin periodinane Di-pi-methane rearrangement
Diazoalkane 1,3-dipolar cycloaddition Dieckmann condensation
Diels Reese reaction Diels–Alder reaction
Dimroth rearrangement Directed ortho metalation
Doebner reaction Doebner–Miller reaction
Dowd–Beckwith ring-expansion reaction Duff reaction
Dyotropic reaction Edman degradation
Einhorn–Brunner reaction Elbs persulfate oxidation
Electrophilic amination Electrophilic halogenation
Emde degradation Enantioselective synthesis
Enyne metathesis Erlenmeyer–Plchl azlactone or amino-acid synthesis
Eschweiler–Clarke reaction Etard reaction
Favorskii reaction Favorskii rearrangement
Fehling's solution Feist–Benary synthesis
Ferrier carbocyclization Ferrier rearrangement
Finkelstein reaction Fischer glycosidation
Fischer indole synthesis Fischer oxazole synthesis
Fischer–Hepp rearrangement Fischer–Speier esterification
Fleming–Tamao oxidation Formox Process
Forster–Decker method Friedel–Crafts reaction
Friedlander synthesis Fries rearrangement
Fritsch–Buttenberg–Wiechell rearrangement Fujimoto–Belleau reaction
Fukuyama coupling Fukuyama indole synthesis
Fukuyama reduction Gabriel synthesis
Gabriel–Colman rearrangement Gallagher–Hollander degradation
Gassman indole synthesis Gattermann reaction
Gattermann–Koch reaction Gewald reaction
Gilman reagent Glaser coupling
Glycol cleavage Gomberg–Bachmann reaction
Gould–Jacobs reaction Grignard reaction
Grundmann aldehyde synthesis Guerbet reaction
Haber–Weiss reaction Haloform reaction
Halogen addition reaction Halohydrin formation reaction
Hammick reaction Hantzsch pyridine synthesis
Hantzsch pyrrole synthesis Hayashi rearrangement
Heck reaction Hell–Volhard–Zelinsky halogenation
Hemetsberger indole synthesis Herz reaction
Hinsberg oxindole synthesis Hinsberg reaction
Hoesch reaction Hofmann elimination
Hofmann rearrangement Hofmann–Loffler reaction
Hofmann–Martius rearrangement Hooker reaction
Horner–Wadsworth–Emmons reaction Hunsdiecker reaction
Hydration reaction Hydrazone iodination
Hydroamination Hydroboration–oxidation reaction
Hydrohalogenation Ishikawa reagent
Ivanov reaction Jacobsen epoxidation
Jacobsen rearrangement Japp–Klingemann reaction
Japp–Maitland condensation Jones oxidation
Julia olefination Kabachnik–Fields reaction
Ketone halogenation Knoevenagel condensation
Knorr pyrrole synthesis Knorr quinoline synthesis
Kochi reaction Koenigs–Knorr reaction
Kolbe electrolysis Kolbe–Schmitt reaction
Kornblum oxidation Kornblum–DeLaMare rearrangement
Kostanecki acylation Kowalski ester homologation
Krapcho decarboxylation Kulinkovich reaction
Larock indole synthesis Lehmstedt–Tanasescu reaction
Leimgruber–Batcho indole synthesis Letts nitrile synthesis
Leuckart reaction Leuckart thiophenol reaction
Liebeskind–Srogl coupling Lossen rearrangement
Luche reduction Madelung synthesis
Malonic ester synthesis Mannich reaction
Markó–Lam deoxygenation Martinet dioxindole synthesis
McFadyen–Stevens reaction McMurry reaction
Meerwein arylation Meerwein–Ponndorf–Verley reduction
Menshutkin reaction Metal-ion-catalyzed s-bond rearrangement
Meyer–Schuster rearrangement Michael reaction
Michaelis-Arbuzov reaction Michaelis–Arbuzov reaction
Milas hydroxylation Mitsunobu reaction
Mukaiyama aldol addition Nazarov cyclization reaction
Neber rearrangement Nef reaction
Negishi coupling Nenitzescu indole synthesis
Nicholas reaction Niementowski quinazoline synthesis
Nierenstein reaction NIH shift
Nitration Nitroaldol reaction
Noyori asymmetric hydrogenation Olah reagent
Oppenauer oxidation Oxidation of secondary alcohols to ketones
Oxymercuration reaction Paal–Knorr synthesis
Passerini reaction Paterno–Buchi reaction
Pauson–Khand reaction Payne rearrangement
Pechmann condensation Pellizzari reaction
Phenol formaldehyde resin Radical-nucleophilic aromatic substitution
Reductive amination Robinson annulation
Sakurai reaction Schmidt reaction
Schotten–Baumann reaction Seyferth–Gilbert homologation
Smiles rearrangement Sommelet reaction
Staudinger reaction Stephen aldehyde synthesis
Stetter reaction Stevens rearrangement
Stieglitz rearrangement Stille reaction
Stolle synthesis Stork enamine alkylation
Strecker amino-acid synthesis Strecker degradation
Suzuki reaction Swern oxidation
Takai olefination Thiol-yne reaction
Thorpe reaction Tiffeneau–Demjanov rearrangement
Tishchenko reaction Transesterification
Ugi reaction Ullmann condensation
Ullmann reaction Upjohn dihydroxylation
Urech hydantoin synthesis Vilsmeier–Haack reaction
Volhard–Erdmann cyclization Von Braun amide degradation
Von Braun reaction Von Richter reaction
Wagner-Jauregg reaction Wagner–Meerwein rearrangement
Wallach rearrangement Weerman degradation
Wenker synthesis Westphalen–Lettre rearrangement
Wharton reaction Whiting reaction
Wilkinson's catalyst Willgerodt rearrangement
Williamson ether synthesis Wittig reaction
Wohl degradation Wohl–Aue reaction
Wohl–Ziegler bromination Wolff rearrangement
Wolff–Kishner reduction Wolffenstein–Boters reaction
Woodward cis-hydroxylation Wulff–Dotz reaction
Wurtz reaction Wurtz–Fittig reaction
Yamaguchi esterification Zeisel determination
Zerewitinoff determination Zincke nitration
Zincke reaction Zincke–Suhl reaction
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