User:Iamnhm/Books/~Organic Chemistry~
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~Organic Chemistry~[edit]
Reactions[edit]
- 1,3-Butadiene
- 1,3-Dipolar cycloaddition
- 1-Fluoro-2,4-dinitrobenzene
- 2,3-Wittig rearrangement
- 2-Pyridone
- Acetal
- Acetylene
- Acetylide
- Achmatowicz reaction
- Acylation
- Acyloin condensation
- Adams decarboxylation
- Adams's catalyst
- Adkins–Peterson reaction
- Akabori amino-acid reaction
- Alcohol oxidation
- Aldehyde
- Aldol condensation
- Aldol reaction
- Algar–Flynn–Oyamada reaction
- Alkylimino-de-oxo-bisubstitution
- Alkyne trimerisation
- Alkyne zipper reaction
- Allan–Robinson reaction
- Allylic rearrangement
- Amadori rearrangement
- Amide
- Amine alkylation
- Amine oxide
- Andrussow process
- Angeli–Rimini reaction
- Anthraquinone
- Antimony trifluoride
- Appel reaction
- Arene substitution pattern
- Arndt–Eistert reaction
- Aromatic sulfonation
- Asymmetric induction
- Auwers synthesis
- Azide
- Aziridine
- Azo coupling
- Azulene
- 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
- Bargellini reaction
- Bartoli indole synthesis
- Barton reaction
- Barton–Kellogg reaction
- Barton–McCombie deoxygenation
- Barton–Zard reaction
- Baudisch reaction
- Baylis–Hillman reaction
- Bechamp reaction
- Bechamp reduction
- Beckmann rearrangement
- Belousov–Zhabotinsky reaction
- Benary reaction
- Benedict's reagent
- Benkeser reaction
- Benzidine
- Benzilic acid rearrangement
- Benzofuran
- Benzoin condensation
- Bergman cyclization
- Bergmann azlactone peptide synthesis
- Bergmann degradation
- Bernthsen acridine synthesis
- Betti reaction
- Biginelli reaction
- Bingel reaction
- Birch reduction
- Bischler–Möhlau indole synthesis
- Bischler–Napieralski reaction
- Biuret test
- Blaise ketone synthesis
- Blaise reaction
- Blanc chloromethylation
- Bodroux–Chichibabin aldehyde synthesis
- Boord olefin synthesis
- Boronic acid
- Bosch reaction
- Bouveault aldehyde synthesis
- Bouveault–Blanc reduction
- Boyland–Sims oxidation
- Bredt's rule
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer–Bergs reaction
- Buchner ring expansion
- Buchwald–Hartwig amination
- Büchner–Curtius–Schlotterbeck reaction
- Cadiot–Chodkiewicz coupling
- Camps quinoline synthesis
- Cannizzaro reaction
- Carbazole
- Carbohydrate acetalisation
- Carbon monoxide
- Carbonyl reduction
- Carbonylation
- Carboxybenzyl
- Carboxylic acid
- Carbylamine reaction
- Carroll rearrangement
- Cascade reaction
- Castro–Stephens coupling
- Catalytic reforming
- Catellani reaction
- CBS catalyst
- Cheletropic reaction
- Chichibabin pyridine synthesis
- Chichibabin reaction
- Chiral auxiliary
- Chiral pool synthesis
- Chugaev elimination
- Claisen condensation
- Claisen rearrangement
- Clemmensen reduction
- Collins reagent
- Combes quinoline synthesis
- Conrad–Limpach synthesis
- Cook–Heilbron thiazole synthesis
- Cope reaction
- Cope rearrangement
- Copper chromite
- Corey–Fuchs reaction
- Corey–House synthesis
- Corey–Itsuno reduction
- Corey–Kim oxidation
- Corey–Winter olefin synthesis
- Coupling reaction
- Cracking (chemistry)
- Creighton process
- Criegee rearrangement
- Cumene process
- Curtius rearrangement
- Cyanohydrin reaction
- Cyclooctadecanonaene
- Cyclopropanation
- Cyclopropane
- Dakin–West reaction
- Danheiser annulation
- Danheiser benzannulation
- Darzens halogenation
- Darzens reaction
- Dehydration reaction
- Dehydrogenation
- Delépine reaction
- Demjanov rearrangement
- Dess–Martin oxidation
- Dess–Martin periodinane
- Di-pi-methane rearrangement
- Diazoalkane 1,3-dipolar cycloaddition
- Diazonium compound
- Dieckmann condensation
- Diels–Alder reaction
- Diels–Reese reaction
- Diisobutylaluminium hydride
- Dimethyl sulfate
- Dimroth rearrangement
- Diphosphorus tetraiodide
- Directed ortho metalation
- Doebner reaction
- Doebner–Miller reaction
- Doering–LaFlamme allene synthesis
- Dowd–Beckwith ring-expansion reaction
- Duff reaction
- Dyotropic reaction
- E1cB-elimination reaction
- Edman degradation
- Einhorn–Brunner reaction
- Elbs persulfate oxidation
- Elbs reaction
- Electrochemical fluorination
- Electrocyclic reaction
- Electrophilic amination
- Electrophilic aromatic directing groups
- Electrophilic halogenation
- Electrosynthesis
- Elimination reaction
- Emde degradation
- Enantioselective synthesis
- Ene reaction
- Enyne metathesis
- Epoxide
- Erlenmeyer–Plöchl azlactone and amino-acid synthesis
- Eschenmoser fragmentation
- Eschweiler–Clarke reaction
- Ester pyrolysis
- Ether
- Favorskii reaction
- Favorskii rearrangement
- Fehling's solution
- Feist–Benary synthesis
- Fenton's reagent
- Ferrier carbocyclization
- Ferrier rearrangement
- Finkelstein reaction
- Fischer glycosidation
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fischer–Hepp rearrangement
- Fischer–Speier esterification
- Fischer–Tropsch process
- Fleming–Tamao oxidation
- Fluorination with aminosulfuranes
- Fluorocarbon
- Folin–Ciocalteu reagent
- Formox process
- Forster–Decker method
- Free-radical halogenation
- Free-radical reaction
- Friedel–Crafts reaction
- Friedländer 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
- Geminal halide hydrolysis
- Gewald reaction
- Gilman reagent
- Glaser coupling
- Glycol cleavage
- Gomberg–Bachmann reaction
- Gould–Jacobs reaction
- Grignard reaction
- Grob fragmentation
- Grubbs' catalyst
- Grundmann aldehyde synthesis
- Guerbet reaction
- Haber–Weiss reaction
- Haloform reaction
- Halogen addition reaction
- Halohydrin
- Hammett equation
- Hammick reaction
- Hammond's postulate
- Hantzsch pyridine synthesis
- Hantzsch pyrrole synthesis
- Hayashi rearrangement
- Heck reaction
- Helferich method
- Hell–Volhard–Zelinsky halogenation
- Hemetsberger indole synthesis
- Herz reaction
- Hinsberg oxindole synthesis
- Hinsberg reaction
- Hoesch reaction
- Hofmann elimination
- Hofmann rearrangement
- Hofmann–Löffler reaction
- Hofmann–Martius rearrangement
- Hooker reaction
- Horner–Wadsworth–Emmons reaction
- Hunsdiecker reaction
- Hydration reaction
- Hydrazone iodination
- Hydroamination
- Hydroboration
- Hydroboration–oxidation reaction
- Hydrodesulfurization
- Hydroformylation
- Hydrogenolysis
- Hydrohalogenation
- Hydrosilylation
- Indigo dye
- Indium-mediated allylation
- Isatin
- Ishikawa reagent
- Isocyanide
- Isomer
- Ivanov reaction
- Jacobsen epoxidation
- Jacobsen rearrangement
- Japp–Klingemann reaction
- Japp–Maitland condensation
- Jones oxidation
- Julia olefination
- Kabachnik–Fields reaction
- Ketene
- Ketone
- Ketone halogenation
- Kharasch–Sosnovsky reaction
- Kiliani–Fischer synthesis
- 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
- Kröhnke pyridine synthesis
- Kulinkovich reaction
- Kumada coupling
- Larock indole synthesis
- Lehmstedt–Tanasescu reaction
- Leimgruber–Batcho indole synthesis
- Letts nitrile synthesis
- Leuckart reaction
- Leuckart thiophenol reaction
- Liebeskind–Srogl coupling
- Lindlar catalyst
- List of organic reactions
- Lobry de Bruyn–van Ekenstein transformation
- Lossen rearrangement
- Lucas' reagent
- Luche reduction
- Madelung synthesis
- Maillard reaction
- Malaprade reaction
- Malonic ester synthesis
- Mannich reaction
- Markovnikov's rule
- Markó–Lam deoxygenation
- Martinet dioxindole synthesis
- McFadyen–Stevens reaction
- McMurry reaction
- Meerwein arylation
- Meerwein–Ponndorf–Verley reduction
- Meisenheimer complex
- Melamine
- Menshutkin reaction
- Mercury(I) chloride
- Mesylate
- Methylation
- Meyer–Schuster rearrangement
- Michael reaction
- Michaelis–Arbuzov reaction
- Milas hydroxylation
- Minisci reaction
- Mitsunobu reaction
- Molisch's test
- Mukaiyama aldol addition
- Nazarov cyclization reaction
- Neber rearrangement
- Nef reaction
- Negishi coupling
- Nenitzescu indole synthesis
- Nicholas reaction
- Niementowski quinazoline synthesis
- Niementowski quinoline synthesis
- Nierenstein reaction
- NIH shift
- Ninhydrin
- Nitration
- Nitrile
- Nitrite
- Nitro compound
- Nitroaldol reaction
- Nitrone-olefin (3+2) cycloaddition
- Nitrosobenzene
- Noyori asymmetric hydrogenation
- Nozaki–Hiyama–Kishi reaction
- Nucleophilic acyl substitution
- Nucleophilic aromatic substitution
- Olah reagent
- Olefin metathesis
- Oppenauer oxidation
- Organocopper compound
- Organomercury
- Organoselenium chemistry
- Organosilicon
- Organosodium chemistry
- Organosulfur compounds
- Organozinc compound
- Osazone
- Oxidation of secondary alcohols to ketones
- Oxime
- Oxy-Cope rearrangement
- Oxymercuration reaction
- Ozonolysis
- Paal–Knorr synthesis
- Pagodane
- Passerini reaction
- Paternò–Büchi reaction
- Pauson–Khand reaction
- Payne rearrangement
- Pechmann condensation
- Pellizzari reaction
- Peptide synthesis
- Periodinane
- Perkin reaction
- Perkow reaction
- Petasis reagent
- Peterson olefination
- Petrenko-Kritschenko piperidone synthesis
- Pfitzinger reaction
- Pfitzner–Moffatt oxidation
- Phenanthrene
- Phenanthridine
- Phenol formaldehyde resin
- Phenols
- Phenyl salicylate
- Photosynthesis
- Phthalic anhydride
- Piancatelli rearrangement
- Pictet–Spengler reaction
- Pinacol coupling reaction
- Pinacol rearrangement
- Pinner reaction
- Pinner triazine synthesis
- Pinnick oxidation
- Pomeranz–Fritsch reaction
- Porphyrin
- Prato reaction
- Prelog strain
- Prilezhaev reaction
- Prins reaction
- Protecting group
- Prévost reaction
- Pummerer rearrangement
- Pyrazine
- Pyrazole
- Pyridine
- Pyrrole
- Pyruvate dehydrogenase
- Quelet reaction
- Racemization
- Radical-nucleophilic aromatic substitution
- Ramberg–Bäcklund reaction
- Raney nickel
- Raschig–Hooker process
- Rauhut–Currier reaction
- Reductive amination
- Reductive dehalogenation of halo ketones
- Reed reaction
- Reformatsky reaction
- Reimer–Tiemann reaction
- Reissert indole synthesis
- Reissert reaction
- Rieche formylation
- Riemschneider thiocarbamate synthesis
- Ritter reaction
- Robinson annulation
- Robinson–Gabriel synthesis
- Rosenmund reduction
- Rosenmund–von Braun reaction
- Rubottom oxidation
- Ruzicka large-ring synthesis
- Sakurai reaction
- Salicylaldehyde
- Salt metathesis reaction
- Sandmeyer reaction
- Saponification
- Sarett oxidation
- Schiff base
- Schiff test
- Schlenk equilibrium
- Schmidt reaction
- Scholl reaction
- Schotten–Baumann reaction
- Seliwanoff's test
- Seyferth–Gilbert homologation
- Shapiro reaction
- Sharpless asymmetric dihydroxylation
- Sharpless epoxidation
- Sharpless oxyamination
- Sigmatropic reaction
- Silyl ether
- Simmons–Smith reaction
- Skraup reaction
- Smiles rearrangement
- SN1 reaction
- SN2 reaction
- SNi
- Solvolysis
- Sommelet reaction
- Sonogashira coupling
- Staudinger reaction
- Steglich esterification
- Stephen aldehyde synthesis
- Stetter reaction
- Stevens rearrangement
- Stieglitz rearrangement
- Stille reaction
- Stollé synthesis
- Stork enamine alkylation
- Strain (chemistry)
- Strecker amino acid synthesis
- Strecker degradation
- Sulfonate
- Sulfur mustard
- Suzuki reaction
- Swain equation
- Swern oxidation
- Sørensen formol titration
- Takai olefination
- Talk:Petasis reaction
- Tebbe's reagent
- Terephthalic acid
- Tetralin
- Tetrapropylammonium perruthenate
- Triphenylmethyl radical
- Tropinone
- Tryptamine
- Ullmann condensation
- Urea
- Wagner–Meerwein rearrangement
- Willgerodt rearrangement
- Wittig reaction
- Wohl degradation
- Wolffenstein–Böters reaction
- Wulff–Dötz reaction
- Zaitsev's rule
- Étard reaction
- 1,4-Benzoquinone
- Thiol-yne reaction
- Thorpe reaction
- Tiffeneau–Demjanov rearrangement
- Tishchenko reaction
- Aldol–Tishchenko reaction
- Tollens' reagent
- Transfer hydrogenation
- Trapp mixture
- Transesterification
- Purine
- Hydrolysis
- Ugi reaction
- Ullmann reaction
- Upjohn dihydroxylation
- Urech hydantoin synthesis
- Van Slyke determination
- Varrentrapp reaction
- Vilsmeier–Haack reaction
- Acyloin
- Volhard–Erdmann cyclization
- Von Braun amide degradation
- Von Braun reaction
- Cinnoline
- Von Richter reaction
- Wacker process
- Wagner-Jauregg reaction
- Walden inversion
- Wallach rearrangement
- Weerman degradation
- Weinreb ketone synthesis
- Wenker synthesis
- Flavones
- Westphalen–Lettré rearrangement
- Wharton reaction
- Whiting reaction
- Wilkinson's catalyst
- Williamson ether synthesis
- 2-Norbornyl cation
- 1,2-Wittig rearrangement
- Wohl–Aue reaction
- Wöhler synthesis
- Wohl–Ziegler bromination
- Wolff rearrangement
- Wolff–Kishner reduction
- Woodward cis-hydroxylation
- Woodward–Hoffmann rules
- Wurtz reaction
- Wurtz–Fittig reaction
- Yamaguchi esterification
- Zeisel determination
- Zerewitinoff determination
- Disulfide
- Zincke nitration
- Zincke reaction
- Zincke–Suhl reaction
- Zinin reaction