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In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes, ketones and carboxylic acid), as part of many larger functional groups. A compound containing a ...
Most metal carbonyl complexes contain a mixture of ligands. Examples include the historically important IrCl(CO)(P(C 6 H 5) 3) 2 and the antiknock agent (CH 3 C 5 H 4)Mn(CO) 3. The parent compounds for many of these mixed ligand complexes are the binary carbonyls, those species of the formula [M x (CO) n] z, many of which are
Carbonyl sulfide is the chemical compound with the linear formula O=C=S. It is a colorless flammable gas with an unpleasant odor . [ not verified in body ] It is a linear molecule consisting of a carbonyl double bonded to a sulfur atom.
Carbon compounds are defined as chemical substances containing carbon. [1] [2] More compounds of carbon exist than any other chemical element except for hydrogen. Organic carbon compounds are far more numerous than inorganic carbon compounds. In general bonds of carbon with other elements are covalent bonds.
General structure of 1,2-, 1,3-, and 1,4-dicarbonyls. In organic chemistry, a dicarbonyl is a molecule containing two carbonyl (C=O) groups.Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4 ...
Triruthenium dodecacarbonyl is the chemical compound with the formula Ru 3 (CO) 12. Classified as metal carbonyl cluster, it is a dark orange-colored solid that is soluble in nonpolar organic solvents. The compound serves as a precursor to other organoruthenium compounds.
Dicobalt octacarbonyl is an organocobalt compound with composition Co 2 (CO) 8. This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry. [2] [3] It is the parent member of a family of hydroformylation catalysts. [4]
The carbonyl group is polar because the electronegativity of the oxygen is greater than that for carbon. Thus, ketones are nucleophilic at oxygen and electrophilic at carbon. Because the carbonyl group interacts with water by hydrogen bonding, ketones are typically more soluble in water than the related methylene compounds. Ketones are hydrogen ...