Carbene: Structure, Preparation, Reactions, Applications
A carbene is a molecule that has a neutral carbon atom with a valence of two and two unshared valence electrons. They are neutral transitory carbon intermediates. They have two … Read more
Organic chemistry is a branch of chemistry that examines the structure, characteristics, and interactions of organic molecules that have covalent bonds with carbon.
A carbene is a molecule that has a neutral carbon atom with a valence of two and two unshared valence electrons. They are neutral transitory carbon intermediates. They have two … Read more
Chugaev reaction is a chemical process that eliminates water from an alcohol, resulting in the formation of an alkene. Xanthate is the intermediate. It is named after Russian chemist Lev … Read more
Combinatorial synthesis is a synthesis technique that allows for the generation of a large number of related molecules at the same time. These collections are known as libraries, and they … Read more
N-Bromosuccinimide (NBS) is a useful organic chemistry reagent. NBS has traditionally been thought of as a convenient supply of either cationic bromine for electrophilic addition processes or a bromine radical … Read more
The Benzoin Condensation is a coupling reaction between two aldehydes that produces α-hydroxyketones. Only aromatic aldehydes could be converted using the initial procedures. The condensation of two molecules of benzaldehyde … Read more
Knoevenagel condensation is the nucleophilic addition of an active hydrogen compound to a carbonyl group, followed by a dehydration process that eliminates a molecule of water. The result is frequently … Read more
Coumarin is a naturally occurring substance belonging to the benzopyrone family. It is also known as 1-benzopyran-2-one. Vogel identified the first parent coumarin from tonka bean (Dipteryx odorata) in 1820. The … Read more
Diazotization reaction is the reaction that produces diazonium ions from aromatic amines. The process of creating a diazonium salt or diazonium compound is known as diazotization. An aromatic amine combines … Read more
The Sandmeyer reaction is a form of radical-nucleophilic aromatic substitution process. It’s a valuable tool for replacing an amino group on an aromatic ring with alternative substituents. This reaction converts … Read more