User:Anwarasif/Books/Organic Chemistry

Organic Reactions

 * 1,2-Wittig rearrangement
 * 1,3-Butadiene
 * 1,3-Dipolar cycloaddition
 * 1,4-Benzoquinone
 * 1-Fluoro-2,4-dinitrobenzene
 * 2,3-Wittig rearrangement
 * 2-Norbornyl cation
 * 2-Pyridone
 * Acetal
 * Acetylene
 * Acetylide
 * Achmatowicz reaction
 * Acylation
 * Acyloin
 * 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
 * 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 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
 * 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
 * Cinnoline
 * 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 oxidation
 * Dakin–West reaction
 * Danheiser annulation
 * Darzens halogenation
 * Darzens reaction
 * Dehydration reaction
 * Dehydrogenation
 * Delépine reaction
 * Demjanov rearrangement
 * Dess–Martin periodinane
 * Di-pi-methane rearrangement
 * Diazoalkane 1,3-dipolar cycloaddition
 * Diazonium compound
 * Dichlorocarbene
 * Dieckmann condensation
 * Diels–Alder reaction
 * Diels–Reese reaction
 * Diisobutylaluminium hydride
 * Dimethyl sulfate
 * Dimroth rearrangement
 * Dipeptide
 * Diphosphorus tetraiodide
 * Directed ortho metalation
 * Disulfide bond
 * Doebner reaction
 * Doebner–Miller reaction
 * 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 aromatic substitution
 * 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
 * Flavones
 * 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 formation reaction
 * 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
 * Hydrolysis
 * Hydrosilylation
 * Indigo dye
 * Indium-mediated allylation
 * Isatin
 * Ishikawa reagent
 * Isocyanide
 * Isomer
 * Isoquinoline
 * 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
 * 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
 * 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
 * Metal-ion-catalyzed σ-bond rearrangement
 * 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
 * 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 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
 * Pomeranz–Fritsch reaction
 * Porphyrin
 * Prato reaction
 * Prelog strain
 * Prins reaction
 * Protecting group
 * Prévost reaction
 * Pummerer rearrangement
 * Purine
 * 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
 * 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
 * Tebbe's reagent
 * Terephthalic acid
 * Tetralin
 * Tetrapropylammonium perruthenate
 * Thiol-yne reaction
 * Thorpe reaction
 * Tiffeneau–Demjanov rearrangement
 * Tishchenko reaction
 * Tollens' reagent
 * Transesterification
 * Transfer hydrogenation
 * Trapp mixture
 * Triphenylmethyl radical
 * Tropinone
 * Tryptamine
 * Ugi reaction
 * Ullmann condensation
 * Ullmann reaction
 * Upjohn dihydroxylation
 * Urea
 * Urech hydantoin synthesis
 * Van Slyke determination
 * Varrentrapp reaction
 * Vilsmeier–Haack reaction
 * Volhard–Erdmann cyclization
 * Von Braun amide degradation
 * Von Braun reaction
 * Von Richter reaction
 * Wacker process
 * Wagner-Jauregg reaction
 * Wagner–Meerwein rearrangement
 * Walden inversion
 * Wallach rearrangement
 * Weerman degradation
 * Weinreb ketone synthesis
 * Wenker synthesis
 * Westphalen–Lettré 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
 * Wolffenstein–Böters reaction
 * Wolff–Kishner reduction
 * Woodward cis-hydroxylation
 * Woodward–Hoffmann rules
 * Wulff–Dötz reaction
 * Wurtz reaction
 * Wurtz–Fittig reaction
 * Wöhler synthesis
 * Yamaguchi esterification
 * Zaitsev's rule
 * Zeisel determination
 * Zerewitinoff determination
 * Zincke nitration
 * Zincke reaction
 * Zincke–Suhl reaction
 * Zinin reaction
 * Étard reaction