Category:Organic chemistry

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Organic chemistry

Organic chemistry is the study of organic, or carbon based, molecules. Carbon is the only element that can make bonds with itself so that chains are produced, silicon has similar properties, but Carbon is a main element in everyday life, and thus, is lucky enough to have a whole subject in chemistry dedicated to it.

Subcategories

There are 8 subcategories to this category shown below (more may be shown on subsequent pages).

F Functional groups O Organic compounds

O cont. Organic reactions Organometallic chemistry R Reagents for organic chemistry

S Stereochemistry T Total synthesis µ Organic chemistry stubs

Pages in category "Organic chemistry"

There are 149 pages in this section of this category.

List of important publications in chemistry * Organic chemistry Chlorinated paraffins 1 1,3-dipole A Aglycon Alicyclic compound Alkyl cycloalkane Alpha carbon Amino sugar Angle strain Annulation Anomer Anomeric effect Anti addition Antiaromaticity Aroma compound Aromatic compound Aryne Autoxidation Azide alkyne Huisgen cycloaddition B Backbone chain Baeyer strain theory Baldwin's rules Bechgaard salt Beilstein database Benedict's reagent Beta-silicon effect Betaines Bicyclic molecule Biocatalysis Branching (chemistry) Bredt's Rule C Cahn-Ingold-Prelog priority rule Captodative Effect Carbanion Carbene Carbenoid Carbon-carbon bond Carboxylic acid Carbyne Cascade reaction Charge transfer complex Chemical decomposition Chiral pool synthesis Chiral synthesis Click chemistry Combustion analysis Conformational isomerism Conjugated system

C cont. Cracking (chemistry) Cumene process D Deep eutectic solvent Degree of unsaturation Diphenylketene Disrotatory Dynamic covalent chemistry E Electrofuge Enantiomer Enol Extended Huckel method F Fehling's solution Functional group Functional isomer G Glycoside hydrolase H Hammett equation Hetero atom Homoaromaticity Homologous series Hydrodealkylation Hyperconjugation Hückel method Hückel's rule I IUPAC nomenclature of organic chemistry Intramolecular Ion exchange resin Ionic liquid Isomer K Keto-enol tautomerism Kinetic isotope effect L Leaving group M Macrocycle Mannich base Markovnikov's rule Meisenheimer complex Molecular knot Monoterpene Mutarotation N Neighbouring group participation Nitrene Non-Kekulé molecule Non-classical ion Nucleofuge Nucleophile O On water reaction Optical rotation Organic compound Organic reaction Organic synthesis Osazone

P Pariser–Parr–Pople method Peptide synthesis Periodinane Persistent carbene Phenols Plant hormone Platonic hydrocarbons Polar effect Polycyclic compound Porphin Protecting group Push-pull olefin R Radical ion Random coil Regioselectivity Resonance (chemistry) Retrosynthetic analysis Ring strain S Saponification Schiff base Schlenk equilibrium Side chain Singlet oxygen Skeletal formula Soil organic matter Solid-phase synthesis Solvated electron Spiro compound Stacking (chemistry) Stereoselectivity Substituent Substitution (chemistry) Syn addition Synthon T Tautomer Terpene Transannular interaction Transition state Trapp mixture Triphenylmethyl radical Triplet oxygen U Ultraviolet light absorber Umpolung Unsaponifiable Unsaturated compound V Van Slyke determination W Woodward-Hoffmann rules Z Zaitsev's rule Zeisel determination Zerewitinoff determination

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Category: Chemistry

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