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Organic chemistry[edit]

Chemical bond: Orbital hybridisation; Chemical bond; Conformational isomerism; Cyclohexane conformation; Cis–trans isomerism; Chirality (chemistry); Axial chirality; Planar chirality; Inherent chirality; Stereochemistry; Stereoisomerism; Absolute configuration; Enantiomer; Fischer projection; Chemical polarity; Formal charge; Resonance (chemistry); Oxidation state; Dissociation constant; Lewis acids and bases; Organic acid; Organic reaction; Addition reaction; Elimination reaction; Substitution reaction; Rearrangement reaction; Radical (chemistry); Radical initiator; Ion; Inductive effect; Electrophile; Nucleophile; Carbocation; Carbanion
Alkanes: Alkane; Free-radical halogenation; Cycloalkane; Petrochemical; Reed reaction; N-Bromosuccinimide; Regioselectivity; Carbene; Simmons–Smith reaction; Sigmatropic reaction
Alkenes: Alkene; Electrophilic addition; Allyl group; Halogen addition reaction; Hydrogenation; Markovnikov's rule; Hydrohalogenation; Oxymercuration reaction; Hydroboration; Hydroboration–oxidation reaction; Halohydrin; Free-radical addition; Cycloalkene; Cyclooctene; Epoxide; Ozonolysis; Dihydroxylation; Diene; Thermodynamic versus kinetic reaction control; Diels–Alder reaction; Polar effect; Adamantane; Nucleophilic addition; Polymer; Tacticity
Alkynes: Alkyne; Alkyne trimerisation; Cycloalkyne; Keto–enol tautomerism; Nickel boride
Aromates: Aromatic hydrocarbon; Aromaticity; Hückel's rule; Homoaromaticity; Electrophilic aromatic substitution; Friedel–Crafts reaction; Wolff–Kishner reduction; Clemmensen reduction; Aromatic sulfonation; Oleum; Nitrosation; Nucleophilic aromatic substitution; Azo coupling; Cumene process; Maleic anhydride; Raney nickel; Lithium aluminium hydride; Diisobutylaluminium hydride; Birch reduction
Halogen derivatives: Haloalkane; Haloform reaction; Nucleophilic substitution; Finkelstein reaction; Gabriel synthesis; 4-Toluenesulfonyl chloride; Mitsunobu reaction; Sandmeyer reaction; Gattermann reaction; Balz–Schiemann reaction
Organometals: Organometallic chemistry; Grignard reaction; Peroxy acid; Gilman reagent; Transmetalation; Directed ortho metalation; Trimethylsilyl chloride; Wurtz reaction; Wurtz–Fittig reaction; Alcohol; Jones oxidation; Pyridinium chlorochromate; Cornforth reagent; Triethylamine; Barton reaction; Ugi reaction; Diazomethane; Meta-Chloroperoxybenzoic acid; Diazonium compound; Iodolactonization; Tetra-n-butylammonium fluoride; Sodium amide; Sodium azide; Staudinger reaction; Darzens reaction; Frémy's salt; Organosilicon; Claisen rearrangement; Dimethylformamide; Michaelis–Arbuzov reaction; Perkow reaction; Phenols; Alkoxide; Pinacol rearrangement; Wagner–Meerwein rearrangement; Hydroquinone; Phenol formaldehyde resin; Ether; Williamson ether synthesis; Ether cleavage; Cope rearrangement; Oxetane; Morpholine; Ethylene oxide; Polyethylene glycol; Crown ether; Template reaction; Thiol; Sulfene; Sulfone; Dimethyl sulfide; Carbonyl sulfide; Thioether; Disulfide; Sulfoxide; Nucleophilic acyl substitution; Carbonyl group; Tetrahedral carbonyl addition compound; Enol; Lithium diisopropylamide; Acetylacetone; Aldol; Aldol reaction; Aldol condensation; Aldehyde; Ketone; Fehling's solution; Tollens' reagent; Hemiacetal; Acetal; Thioacetal; Hemithioacetal; Cannizzaro reaction; Cyanohydrin; Wittig reaction; Nitro compound; Hydrazone; Hydroxylamine; Oxime; Enamine; Hemiaminal; Imine; Schiff base; Amine; Michael reaction; Nucleophilic conjugate addition; Beckmann rearrangement; Johnson–Corey–Chaykovsky reaction; Tishchenko reaction; Hydroxylammonium chloride; Carboxylic acid; Arndt–Eistert reaction; Amide; Ester; Organic acid anhydride; Thioester; Pseudoacid; Acyl halide; Keto acid; Alpha hydroxy acid; Thiocarboxylic acid; Hydrazide; Hydroxamic acid; Acyl azide; Pinner reaction; Lactone; Lactam; Decarboxylation; Polyester; Fischer–Speier esterification; Transesterification; Aminolysis; Weinreb ketone synthesis; Hofmann rearrangement; Curtius rearrangement; Nitrene; Carbamic acid; Caprolactam; Nylon 6; Baeyer–Villiger oxidation; Malonic ester synthesis; Acetoacetic ester synthesis; Dieckmann condensation; Claisen condensation; Hell–Volhard–Zelinsky halogenation; Carbonyl alpha-substitution reactions; Acyloin condensation; Perkin reaction; Knoevenagel condensation; Acrylonitrile; Dendrimer; Stork enamine alkylation; Robinson annulation; Lactide; Reformatsky reaction; Ritter reaction; Organic synthesis; Organic chemistry; Bis(trimethylsilyl)amine; Carbonyldiimidazole; Mannich reaction; Orthoester; Carbonate ester; Semicarbazide; Urea; Urea-formaldehyde; Barbital; Biuret; Guanidine; Thiourea; N,N'-Dicyclohexylcarbodiimide; Cumulene; Allene; Ketene; Carbamate; Ammonium; Azo compound; Amine oxide; Nitroso; Nitrile; Nitrite; Nitrate ester; Azoxy; Hydrogen bond; Trifluoroacetic acid; Hofmann elimination; Cope reaction; Amino acid; Strecker amino acid synthesis; Dansyl chloride; Edman degradation; Tert-Butyloxycarbonyl protecting group; Carboxybenzyl; Peptide synthesis; Peptide; Lipid; Surfactant; Prostaglandin; Elias James Corey; Terpenoid; Carbohydrate; Mutarotation; Koenigs–Knorr reaction; Aldonic acid; Aldaric acid; Uronic acid; Kiliani–Fischer synthesis; Glycoside; Wohl degradation; Osazone; Disaccharide; Cyclodextrin; Heterocyclic compound; Pyridine; Picoline; Chichibabin reaction; Pyrrole; Thiophene; Furan; Furfural; Pyridazine; Pyrimidine; Pyrazine; Hantzsch pyridine synthesis; Porphyrin; Nucleic acid; Stacking (chemistry); Polymerase chain reaction; Supramolecular chemistry; Intercalation (biochemistry); Liquid crystal; Job plot; Cryptand; Amidine; Calixarene; Thiacalixarene; Rotaxane; Catenane; Pericyclic reaction; HOMO/LUMO; Electrocyclic reaction; Cycloaddition; Coupling reaction; Kumada coupling; Suzuki reaction; Negishi coupling; Sonogashira coupling; Stille reaction; Heck reaction; Adams's catalyst; Alcohol oxidation; Ene reaction; Alkyne zipper reaction; Allylic rearrangement; Benzidine; Carbonyl reduction; Cyanohydrin reaction; Dehydration reaction; Dehydrogenation; Dess–Martin oxidation; Electrophilic halogenation; Electrophilic amination; Arene substitution pattern; Hydroamination; Ketone halogenation; Cyclopropanation; Meisenheimer complex; Methylation; Ninhydrin; Oxy-Cope rearrangement; Oxidation of secondary alcohols to ketones; Protecting group; Retrosynthetic analysis; Total synthesis; Schmidt reaction; Horner–Wadsworth–Emmons reaction; List of organic reactions; List of Nobel laureates
Hydroxy compounds and sulphur analogs
Ethers and sulphur analogs
Carbonyl compunds
Carboxylic acids and their derivatives
Heterocumulenes
Nitrogen derivatives
Biomolecules
Saccharides
Heterocycles
Supramolecules
Pericyclic reactions
Transition metals chemistry