Outline of organic chemistry
The following outline is provided as an overview of and topical guide to organic chemistry:
Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation of carbon-based compounds, hydrocarbons, and their derivatives. These compounds may contain any number of other elements, including hydrogen, nitrogen, oxygen, the halogens as well as phosphorus, silicon, and sulfur.General topics
Current trends in organic chemistry include :
''See also List of organic reactions
- Addition reaction
- *Aldol addition
- *Electrophilic addition
- *Michael Addition
- *Mukaiyama aldol addition
- *Nucleophilic addition
- Cyclization
- *Bergman cyclization
- *Nazarov cyclization reaction
- Elimination reaction
- *Beta elimination
- *Cope elimination
- *E1cB elimination reaction
- *Hofmann elimination
- Organic redox reaction
- *Cannizzaro reaction
- *Oxidation
- **Baeyer-Villiger oxidation
- **Corey-Kim oxidation
- **Dess-Martin oxidation
- **Fleming-Tamao oxidation
- **Jones oxidation
- **Nucleophilic epoxidation
- **Oppenauer oxidation
- **Prilezhaev reaction
- **Rubottom oxidation
- **Schmidt reaction
- **Swern oxidation
- **Wacker-Tsuji oxidation
- *Reduction
- **Birch reduction
- **Bouveault-Blanc reduction
- **CBS reduction
- **Clemmensen reduction
- **Corey-Bakshi-Shibata reduction
- **Corey–Itsuno reduction
- **Fukuyama reduction
- **Luche reduction
- **Meerwein-Ponndorf-Verley reduction
- **Rosenmund reduction
- **Staudinger reduction
- **Wolff-Kishner reduction
- Pericyclic reaction
- *Cheletropic reaction
- *Cycloaddition
- **Azide-alkyne Huisgen cycloaddition
- **1,3-Dipolar cycloaddition
- **Diels–Alder reaction
- **Nitrone-olefin cycloaddition
- **Staudinger Ketene-Imine Cycloaddition
- *Dyotropic reaction
- *Electrocyclic reaction
- *Group transfer reaction
- *Sigmatropic reaction
- Polymerization
- *Ring-opening metathesis polymerisation
- Rearrangement reaction
- *Baker–Venkataraman rearrangement
- *Beckmann rearrangement
- *Benzilic acid rearrangement
- *Brook rearrangement
- *Claisen rearrangement
- *Cope rearrangement
- *Curtius Rearrangement
- *Fries rearrangement
- *Ireland–Claisen rearrangement
- *Newman–Kwart rearrangement
- *Overman rearrangement
- *Oxy-Cope rearrangement
- *Pinacol rearrangement
- *1,2-Wittig rearrangement
- *2,3-Wittig rearrangement
- Substitution reaction
- *Electrophilic aromatic substitution
- *Nucleophilic aromatic substitution
- *Electrophilic substitution
- *Nucleophilic substitution
- **SN1 reaction
- **SN2 reaction
- *Vicarious nucleophilic substitution