User:Antivirak/Books/Org

Organic chemistry

 * 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