User:Awsm1/Books/Name Reactions

Name Reactions

 * List of organic reactions
 * 1,2-Wittig rearrangement
 * 1,3-Dipolar cycloaddition
 * 1-Fluoro-2,4-dinitrobenzene
 * 2,3-Wittig rearrangement
 * 2-Norbornyl cation
 * Acetal
 * Acetylide
 * Acylation
 * Acyloin
 * Acyloin condensation
 * Adams decarboxylation
 * Adams's catalyst
 * Adkins–Peterson reaction
 * Akabori amino-acid reaction
 * Alcohol oxidation
 * Aldehyde
 * 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
 * Amine oxide
 * Andrussow process
 * Angeli–Rimini reaction
 * Antimony trifluoride
 * Appel reaction
 * Arndt–Eistert reaction
 * Asymmetric induction
 * Auwers synthesis
 * Aziridine
 * Baeyer's reagent
 * Baeyer–Villiger oxidation
 * Balz–Schiemann reaction
 * Barton–McCombie deoxygenation
 * Beckmann rearrangement
 * Benedict's reagent
 * Benzidine
 * Benzilic acid rearrangement
 * Benzofuran
 * Benzoin condensation
 * Bodroux–Chichibabin aldehyde synthesis
 * Bouveault aldehyde synthesis
 * Bucherer carbazole synthesis
 * Camps quinoline synthesis
 * Cannizzaro reaction
 * Carbohydrate acetalisation
 * Carbonyl reduction
 * Carbonylation
 * Carboxybenzyl
 * Carbylamine reaction
 * Carroll rearrangement
 * CBS catalyst
 * Chiral auxiliary
 * Claisen condensation
 * Claisen rearrangement
 * Clemmensen reduction
 * Collins reagent
 * Corey–Fuchs reaction
 * Corey–House synthesis
 * Corey–Itsuno reduction
 * Corey–Kim oxidation
 * Corey–Winter olefin synthesis
 * Coupling reaction
 * Cracking (chemistry)
 * Cumene process
 * Curtius rearrangement
 * Cyanohydrin reaction
 * Cyclooctadecanonaene
 * Cyclopropanation
 * Darzens reaction
 * Dehydration reaction
 * Dehydrogenation
 * Di-pi-methane rearrangement
 * Diazoalkane 1,3-dipolar cycloaddition
 * Diazonium compound
 * Dieckmann condensation
 * Diels–Alder reaction
 * Diels–Reese reaction
 * Dimroth rearrangement
 * E1cB-elimination reaction
 * Electrocyclic reaction
 * Electrophilic amination
 * Electrophilic halogenation
 * Elimination reaction
 * Ene reaction
 * Enyne metathesis
 * Epoxide
 * Ester pyrolysis
 * Ether
 * Favorskii reaction
 * Favorskii rearrangement
 * Fehling's solution
 * Ferrier carbocyclization
 * Ferrier rearrangement
 * Finkelstein reaction
 * Fischer–Speier esterification
 * Folin–Ciocalteu reagent
 * Formylation reaction
 * Free-radical halogenation
 * Friedel–Crafts reaction
 * Fries rearrangement
 * Fukuyama reduction
 * Gabriel synthesis
 * Geminal halide hydrolysis
 * Gilman reagent
 * Glycol cleavage
 * Grignard reaction
 * Grundmann aldehyde synthesis
 * Guerbet reaction
 * Haber–Weiss reaction
 * Haloform reaction
 * Halogen addition reaction
 * Hell–Volhard–Zelinsky halogenation
 * Hinsberg oxindole synthesis
 * Hinsberg reaction
 * Hofmann elimination
 * Hofmann rearrangement
 * Hofmann–Löffler reaction
 * Hofmann–Martius rearrangement
 * Hooker reaction
 * Hunsdiecker reaction
 * Hydration reaction
 * Hydrazone iodination
 * Hydroamination
 * Hydroboration
 * Hydrodesulfurization
 * Hydroformylation
 * Hydrogenolysis
 * Hydrohalogenation
 * Hydrosilylation
 * Isatin
 * Ishikawa reagent
 * Isocyanide
 * Isomer
 * Jones oxidation
 * Kabachnik–Fields reaction
 * Ketone
 * Ketone halogenation
 * Kharasch–Sosnovsky reaction
 * Kiliani–Fischer synthesis
 * Kochi reaction
 * Kolbe electrolysis
 * Kolbe–Schmitt reaction
 * Kostanecki acylation
 * Kowalski ester homologation
 * Krapcho decarboxylation
 * Lindlar catalyst
 * Lossen rearrangement
 * Lucas' reagent
 * Luche reduction
 * Malonic ester synthesis
 * Markovnikov's rule
 * McMurry reaction
 * Meerwein arylation
 * Mesylate
 * Metal-ion-catalyzed σ-bond rearrangement
 * Methylation
 * Meyer–Schuster rearrangement
 * Michael reaction
 * Michaelis–Arbuzov reaction
 * Molisch's test
 * Nazarov cyclization reaction
 * Neber rearrangement
 * Nitration
 * Nitroaldol reaction
 * Nucleophilic acyl substitution
 * Nucleophilic aromatic substitution
 * Olah reagent
 * Olefin metathesis
 * Organocopper compound
 * Organomercury
 * Organosulfur compounds
 * Osazone
 * Oxidation of secondary alcohols to ketones
 * Oxime
 * Oxymercuration reaction
 * Ozonolysis
 * Peptide synthesis
 * Periodinane
 * Perkin reaction
 * Petasis reagent
 * Peterson olefination
 * Phenols
 * Phenyl salicylate
 * Phthalic anhydride
 * Piancatelli rearrangement
 * Pinacol coupling reaction
 * Pinacol rearrangement
 * Pinner reaction
 * Pyruvate decarboxylation
 * Quelet reaction
 * Racemization
 * Raney nickel
 * Raschig–Hooker process
 * Reductive amination
 * Reductive dehalogenation of halo ketones
 * Reformatsky reaction
 * Reimer–Tiemann reaction
 * Sandmeyer reaction
 * Saponification
 * Schmidt reaction
 * Schotten–Baumann reaction
 * Seyferth–Gilbert homologation
 * Simmons–Smith reaction
 * SN1 reaction
 * SN2 reaction
 * SNi
 * Sommelet reaction
 * Stephen aldehyde synthesis
 * Stork enamine alkylation
 * Terephthalic acid
 * Thorpe reaction
 * Tiffeneau–Demjanov rearrangement
 * Tishchenko reaction
 * Tollens' reagent
 * Transesterification
 * Transfer hydrogenation
 * Ullmann condensation
 * Upjohn dihydroxylation
 * Volhard–Erdmann cyclization
 * Wagner–Meerwein rearrangement
 * Walden inversion
 * Whiting reaction
 * Willgerodt rearrangement
 * Williamson ether synthesis
 * Wittig reaction
 * Wohl–Ziegler bromination
 * Wolff rearrangement
 * Woodward cis-hydroxylation
 * Woodward–Hoffmann rules
 * Wurtz reaction
 * Wurtz–Fittig reaction
 * Wöhler synthesis
 * Yamaguchi esterification
 * Zaitsev's rule
 * Zincke nitration