User:Awsm1/Books/Name Reactions
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Name Reactions[edit]
- 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