Concept
Amide
Related concepts (47)
Green chemistry
Green chemistry, similar to sustainable chemistry or circular chemistry, is an area of chemistry and chemical engineering focused on the design of products and processes that minimize or eliminate the use and generation of hazardous substances. While environmental chemistry focuses on the effects of polluting chemicals on nature, green chemistry focuses on the environmental impact of chemistry, including lowering consumption of nonrenewable resources and technological approaches for preventing pollution.
Hydrocyanation
In organic chemistry, hydrocyanation is a process for conversion of alkenes to nitriles. The reaction involves the addition of hydrogen cyanide and requires a catalyst. This conversion is conducted on an industrial scale for the production of precursors to nylon. Industrially, hydrocyanation is commonly performed on alkenes catalyzed by nickel complexes of phosphite () ligands. A general reaction is shown: RCH=CH2 + HCN -> RCH2-CH2-CN The reaction involves the addition of and cyanide () to the substrate.
Hydroxamic acid
In organic chemistry, hydroxamic acids are a class of organic compounds bearing the functional group , with R and R' as organic residues. They are amides () wherein the nitrogen center has a hydroxyl () substituent. They are often used as metal chelators. Hydroxamic acids are usually prepared from either esters or acid chlorides by a reaction with hydroxylamine salts. For the synthesis of benzohydroxamic acid, the overall equation is: C6H5CO2Me + NH2OH → C6H5C(O)NHOH + MeOH Hydroxamic acids can also be synthesized from aldehydes and N-sulfonylhydroxylamine via the Angeli-Rimini reaction.
Organyl group
In organic and organometallic chemistry, an organyl group is an organic substituent with one (sometimes more) free valence(-s) at a carbon atom. The term is often used in chemical patent literature to protect claims over a broad scope. Acetonyl group Acyl group (e.g. acetyl group, benzoyl group) Alkyl group (e.g., methyl group, ethyl group) Alkenyl group (e.g.
Acrylamide
Acrylamide (or acrylic amide) is an organic compound with the chemical formula CH2=CHC(O)NH2. It is a white odorless solid, soluble in water and several organic solvents. From the chemistry perspective, acrylamide is a vinyl-substituted primary amide (CONH2). It is produced industrially mainly as a precursor to polyacrylamides, which find many uses as water-soluble thickeners and flocculation agents. Acrylamide forms in burnt areas of food, particularly starchy foods like potatoes, when cooked with high heat, above .
N-Bromosuccinimide
N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution reactions in organic chemistry. NBS can be a convenient source of Br•, the bromine radical. NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates and can be collected by filtration. Crude NBS gives better yield in the Wohl-Ziegler reaction.
2,4-Dinitrophenylhydrazine
2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C6H3(NO2)2NHNH2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene. It can be prepared by the reaction of hydrazine sulfate with 2,4-dinitrochlorobenzene: DNPH is a reagent in instructional laboratories on qualitative organic analysis.