User:Antivirak/Books/Organic chemistry
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Organic chemistry
[edit]- Chemical bond
- Organic chemistry
- 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
- Reaction mechanism
- Organic synthesis
- Addition reaction
- Elimination reaction
- Substitution reaction
- Rearrangement reaction
- Radical (chemistry)
- Radical initiator
- Meta-Chloroperoxybenzoic acid
- Ion
- Inductive effect
- Electrophile
- Nucleophile
- Carbocation
- Carbanion
- Alkanes
- Alkane
- Cycloalkane
- Free-radical halogenation
- N-Bromosuccinimide
- Regioselectivity
- Reed reaction
- Petrochemical
- Carbene
- Simmons–Smith reaction
- Alkenes
- Alkene
- Cycloalkene
- Cyclooctene
- Electrophilic addition
- Allyl group
- Halogen addition reaction
- Hydrogenation
- Markovnikov's rule
- Hydrohalogenation
- Oxymercuration reaction
- Hydroboration
- Hydroboration–oxidation reaction
- Halohydrin
- Free-radical addition
- Epoxide
- Ozonolysis
- Dihydroxylation
- Diene
- Thermodynamic versus kinetic reaction control
- Diels–Alder reaction
- Polar effect
- Adamantane
- Nucleophilic addition
- Polymer
- Tacticity
- Alkynes
- Alkyne
- Cycloalkyne
- Alkyne trimerisation
- 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
- Nucleophilic aromatic substitution
- Nitrosation
- Azo coupling
- Diazonium compound
- Cumene process
- Maleic anhydride
- Raney nickel
- Lithium aluminium hydride
- Diisobutylaluminium hydride
- Birch reduction
- Halogen derivatives
- Haloalkane
- Haloform reaction
- Nucleophilic substitution
- Dimethylformamide
- Sodium amide
- Sodium azide
- Finkelstein reaction
- Gabriel synthesis
- Mitsunobu reaction
- Sandmeyer reaction
- Gattermann reaction
- Balz–Schiemann reaction
- Organometals
- Organometallic chemistry
- Grignard reaction
- Gilman reagent
- Transmetalation
- Directed ortho metalation
- Trimethylsilyl chloride
- Wurtz reaction
- Wurtz–Fittig reaction
- Organosilicon
- Hydroxy compounds and sulphur analogs
- Alcohol
- Phenols
- Alkoxide
- Jones oxidation
- Pyridinium chlorochromate
- Cornforth reagent
- Frémy's salt
- Tetra-n-butylammonium fluoride
- 4-Toluenesulfonyl chloride
- Staudinger reaction
- Darzens reaction
- Claisen rearrangement
- Cope rearrangement
- Wittig reaction
- Horner–Wadsworth–Emmons reaction
- Michaelis–Arbuzov reaction
- Perkow reaction
- Pinacol rearrangement
- Wagner–Meerwein rearrangement
- Hydroquinone
- Phenol formaldehyde resin
- Thiol
- Ethers and sulphur analogs
- Ether
- Williamson ether synthesis
- Ether cleavage
- Oxetane
- Morpholine
- Ethylene oxide
- Polyethylene glycol
- Crown ether
- Template reaction
- Thioether
- Sulfene
- Sulfone
- Dimethyl sulfide
- Carbonyl sulfide
- Disulfide
- Sulfoxide
- Carbonyl compunds
- Carbonyl group
- Tetrahedral carbonyl addition compound
- Aldehyde
- Ketone
- Enol
- Lithium diisopropylamide
- Aldol
- Aldol reaction
- Aldol condensation
- Acetylacetone
- Fehling's solution
- Tollens' reagent
- Hemiacetal
- Acetal
- Hemithioacetal
- Thioacetal
- Cannizzaro reaction
- Cyanohydrin reaction
- Triethylamine
- Enamine
- Hemiaminal
- Imine
- Schiff base
- Amine
- Michael reaction
- Nucleophilic conjugate addition
- Beckmann rearrangement
- Johnson–Corey–Chaykovsky reaction
- Tishchenko reaction
- Hydroxylammonium chloride
- Carboxylic acid
- Iodolactonization
- Diazomethane
- Arndt–Eistert reaction
- Peroxy acid
- Amide
- Ester
- Organic acid anhydride
- Thioester
- Nucleophilic acyl substitution
- Pseudoacid
- Acyl halide
- Nitro compound
- Keto acid
- Alpha hydroxy acid
- Hydroxylamine
- Oxime
- Thiocarboxylic acid
- Hydrazide
- Hydroxamic acid
- Sigmatropic reaction
- Acyl azide
- Pinner reaction
- Lactone
- Lactam
- Decarboxylation
- Polyester
- Fischer–Speier esterification
- Transesterification
- Aminolysis
- Weinreb ketone synthesis
- Hofmann rearrangement
- Curtius rearrangement
- Hydrazone
- 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
- 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
- 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
- List of organic reactions
- List of Nobel laureates
- Carboxylic acids and their derivatives
- Heterocumulenes
- Nitrogen derivatives
- Biomolecules
- Saccharides
- Heterocycles
- Supramolecules
- Pericyclic reactions
- Transition metals chemistry
- Carboximidate