SN1 reaction

0-9 

 1,3-dipolar cycloaddition

A 

 Abramovitch-Shapiro tryptamine synthesis
 Acetoacetic ester condensation
 Achmatowicz reaction
 Acyloin condensation
 Adams catalyst
 Adkins catalyst
 Adkins-Peterson reaction
 Akabori amino acid reaction
 Alder ene reaction
 Alder-Stein rules
 Aldol addition
 Aldol condensation
 Algar-Flynn-Oyamada reaction
 Allan-Robinson reaction
 Allylic rearrangement
 Amadori rearrangement
 Angeli-Rimini reaction
 Andrussov oxidation
 Appel reaction
 Arbuzov reaction, Arbusow reaction
 Arens-van Dorp synthesis, Isler modification
 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-Senguph phenanthrene synthesis
 Bartoli indole synthesis
 Bartoli reaction
 Barton reaction
 Barton-Kellogg reaction
 Barton-McCombie reaction, Barton deoxygenation
 Baudisch reaction
 Bayer test
 Baylis-Hillman reaction
 Bechamp reaction
 Bechamp reduction
 Beckmann fragmentation
 Beckmann rearrangement
 Bellus-Claisen rearrangement
 Belousov-Zhabotinsky reaction
 Benary 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
 Birch reduction
 Bischler-Möhlau indole synthesis
 Bischler-Napieralski reaction
 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
 Buchner-Curtius-Schlotterbeck reaction
 Buchwald-Hartwig amination
 Bunnett reaction

C 

 Cadiot-Chodkiewicz coupling
 Camps quinoline synthesis
 Cannizzaro reaction
 Carroll reaction
 Catalytic reforming
 CBS reduction
 Chan-Lam coupling
 Chapman rearrangement
 Chichibabin pyridine synthesis
 Chichibabin reaction
 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

D 
 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
 Delepine reaction
 Demjanov rearrangement
 Demjanow desamination
 Dess-Martin oxidation
 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

E 
 E1cB elimination reaction
 Eder reaction
 Edman degradation
 Eglinton reaction
 Ehrlich-Sachs reaction
 Einhorn variant
 Einhorn-Brunner reaction
 Elbs persulfate oxidation
 Elbs reaction
 Elimination reaction
 Emde degradation
 Emmert reaction
 Ene reaction
 Epoxidation
 Erlenmeyer synthesis, Azlactone synthesis
 Erlenmeyer-Plöchl azlactone and amino acid synthesis
 Eschenmoser fragmentation
 Eschweiler-Clarke reaction
 Ester pyrolysis
 Étard reaction
 Evans aldol

F 

 Favorskii reaction
 Favorskii rearrangement
 Favorskii-Babayan synthesis
 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
 Forster reaction
 Forster-Decker method
 Franchimont reaction
 Frankland synthesis
 Frankland-Duppa reaction
 Freund reaction
 Friedel-Crafts Acylation
 Friedel-Crafts Alkylation
 Friedländer synthesis
 Fries rearrangement
 Fritsch-Buttenberg-Wiechell rearrangement
 Fujimoto-Belleau reaction
 Fukuyama coupling
 Fukuyama indole synthesis

G 

 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
 Gewald reaction
 Gibbs phthalic anhydride process
 Gilman reagent
 Glaser coupling
 Glycol cleavage
 Gogte synthesis
 Gomberg-Bachmann reaction
 Gomberg-Bachmann-Hey reaction
 Gomberg-Free radical reaction
 Gould-Jacobs reaction
 Graebe-Ullmann synthesis
 Grignard degradation
 Grignard reaction
 Grob fragmentation
 Grubbs' catalyst in Olefin metathesis
 Grundmann aldehyde synthesis
 Gryszkiewicz-Trochimowski and McCombie method
 Guareschi-Thorpe condensation
 Guerbet reaction
 Gutknecht pyrazine synthesis

H 

 Haller-Bauer reaction
 Haloform 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
 Harber-Weiss reaction
 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
 Hinsberg indole synthesis
 Hinsberg oxindole synthesis
 Hinsberg reaction
 Hinsberg separation
 Hinsberg sulfone synthesis
 Hoch-Campbell ethylenimine synthesis
 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
 Hunsdiecker reaction
 Hydroboration
 Hydrohalogenation

I 
 Ing-Manske procedure
 Ipso substitution
 Ivanov reagent, Ivanov reaction

J 

 Jacobsen rearrangement
 Janovsky reaction
 Japp-Klingemann reaction
 Japp-Maitland condensation
 Johnson-Claisen rearrangement
 Jones oxidation
 Jordan-Ullmann-Goldberg synthesis
 Julia olefination
 Julia-Lythgoe olefination

K 

 Kabachnik–Fields reaction
 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
 Kornblum oxidation
 Kornblum–DeLaMare rearrangement
 Kowalski ester homologation
 Krapcho decarboxylation
 Kröhnke aldehyde synthesis
 Kröhnke oxidation
 Kröhnke pyridine synthesis
 Kucherov reaction
 Kuhn-Winterstein reaction
 Kulinkovich reaction
 Kumada coupling

L 

 Larock indole synthesis
 Lebedev process
 Lehmstedt-Tanasescu reaction
 Leimgruber-Batcho indole synthesis
 Letts nitrile synthesis
 Leuckart reaction
 Leuckart thiophenol reaction
 Leuckart-Wallach reaction
 Leuckert amide synthesis
 Levinstein process
 Ley Oxidation
 Lieben iodoform reaction, Haloform reaction
 Liebeskind-Srogl coupling
 Lindlar catalyst
 Lobry-de Bruyn-van Ekenstein transformation
 Lossen rearrangement
 Luche reduction

M 

 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 σ-bond rearrangement
 Mesylation
 Merckwald asymmetric synthesis
 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
 Mukaiyama aldol addition
 Mukaiyama reaction nd sex
 Myers' asymmetric alkylation

N 

 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
 Nitroaldol reaction
 Normant reagents
 Noyori asymmetric hydrogenation
 Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction
 Nucleophilic acyl substitution

O 

 Ohira–Bestmann reaction
 Olefin metathesis
 Oppenauer oxidation
 Ostromyslenskii reaction, Ostromisslenskii reaction
 Oxidative decarboxylation
 Oxo synthesis
 Oxy-Cope rearrangement
 Oxymercuration
 Ozonolysis

P 

 Paal-Knorr pyrrole synthesis
 Paal-Knorr synthesis
 Paneth technique
 Passerini reaction
 Paterno-Büchi reaction
 Pauson-Khand reaction
 Pechmann condensation
 Pechmann pyrazole synthesis
 Pellizzari reaction
 Pelouze 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
 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
 Prelog strain
 Prevost reaction
 Prileschajew reaction
 Prilezhaev reaction
 Prins reaction
 Prinzbach synthesis
 Pschorr reaction
 Pummerer rearrangement
 Purdie methylation, Irvine-Purdie methylation

Q

R 

 Ramberg-Backlund reaction
 Raney-Nickel
 Rap-Stoermer condensation
 Raschig phenol process
 Rauhut–Currier reaction
 Reed reaction
 Reformatskii reaction
 Reilly-Hickinbottom rearrangement
 Reimer-Tiemann reaction
 Reissert indole synthesis
 Reissert reaction, Reissert compound
 Reppe synthesis
 Retropinacol rearrangement
 Riemschneider thiocarbamate synthesis
 Riley oxidations
 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

S 

 Sakurai reaction
 Salol reaction
 Sandheimer
 Sandmeyer diphenylurea isatin synthesis
 Sandmeyer isonitrosoacetanilide isatin synthesis
 Sandmeyer reaction
 Sanger reagent
 Sarett oxidation
 Saytzeff rule, Saytzeff's Rule
 Schiemann reaction
 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
 Semidine rearrangement
 Semmler-Wolff reaction
 Seyferth-Gilbert homologation
 Shapiro reaction
 Sharpless asymmetric dihydroxylation
 Sharpless epoxidation
 Sharpless oxyamination or aminohydroxylation
 Simmons-Smith reaction
 Simonini reaction
 Simonis chromone cyclization
 Skraup chinolin synthesis
 Skraup reaction
 Smiles rearrangement
 SNAr nucleophilic aromatic substitution
 SN1
 SN2
 SNi
 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

T 

 Tamao oxidation
 Tafel rearrangement
 Takai olefination
 Tebbe olefination
 ter Meer reaction
 Thermite reactions
 Thiele reaction
 Thorpe reaction
 Tiemann rearrangement
 Tiffeneau ring enlargement reaction
 Tiffeneau-Demjanow rearrangement
 Tischtschenko reaction
 Tishchenko reaction, Tischischenko-Claisen reaction
 Tollens reagent
 Trapp mixture
 Traube purine synthesis
 Truce-Smiles rearrangement
 Tscherniac-Einhorn reaction
 Tschitschibabin reaction
 Tschugajeff reaction
 Twitchell process
 Tyrer sulfonation process

U 

 Ugi reaction
 Ullmann reaction
 Upjohn dihydroxylation
 Urech cyanohydrin method
 Urech hydantoin synthesis

V 

 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

W 

 Wacker-Tsuji oxidation
 Wagner-Jauregg reaction
 Wagner-Meerwein rearrangement
 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

X

Y 
 Yamaguchi esterification

Z 

 Zeisel determination
 Zerevitinov determination, Zerewitinoff determination
 Ziegler condensation
 Ziegler method
 Zimmermann reaction
 Zincke disulfide cleavage
 Zinke nitration
 Zincke reaction
 Zincke-Suhl reaction

इन्हें भी देखें 
 कार्बनिक यौगिकों की सूची (List of organic compounds)
 अकार्बनिक यौगिकों की सूची (List of inorganic compounds)
 जैविक अणुओं की सूची (List of biomolecules)
 खनिजों की सूची (List of minerals)

बाहरी कड़ियाँ 
 https://web.archive.org/web/20180803014923/https://www.organic-chemistry.org/namedreactions/
 https://web.archive.org/web/20080724052711/http://www.stolaf.edu/depts/chemistry/courses/toolkits/247/practice/medialib/data
 https://web.archive.org/web/20080907063512/http://www.chem.wisc.edu/areas/reich/handouts/namereagents/namedreag-cont.htm

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