Carbonyl group

In organic chemistry, a carbonyl group characterizes the following types of compounds: Other organic carbonyls are urea and the carbamates, the derivatives of acyl chlorides, chloroformates and phosgene, carbonate esters, thioesters, lactones, lactams, hydroxamates, and isocyanates. Examples of inorganic carbonyl compounds are carbon dioxide and carbonyl sulfide. A special group of carbonyl compounds are dicarbonyl compounds, which can exhibit special properties. ==Structure and reactivity==

For organic compounds, the length of the C–O bond does not vary widely from 120 picometers. Inorganic carbonyls have shorter C–O distances: CO, 113; CO2, 116; and COCl2, 116 pm. The carbonyl carbon is typically electrophilic. A qualitative order of electrophilicity is RCHO (aldehydes) > R2CO (ketones) > RCO2R' (esters) > RCONH2 (amides). A variety of nucleophiles attack, breaking the carbon-oxygen double bond. Interactions between carbonyl groups and other substituents were found in a study of collagen. Substituents can affect carbonyl groups by addition or subtraction of electron density by means of a sigma bond. ΔHσ values are much greater when the substituents on the carbonyl group are more electronegative than carbon. The pKa values of acetaldehyde and acetone are 16.7 and 19 respectively, ==Spectroscopy==

• Infrared spectroscopy: the C=O double bond absorbs infrared light at wavenumbers between approximately 1600–1900 cm−1(5263 nm to 6250 nm). The exact location of the absorption is well understood with respect to the geometry of the molecule. This absorption is known as the "carbonyl stretch" when displayed on an infrared absorption spectrum. In addition, the ultraviolet-visible spectra of propanone in water gives an absorption of carbonyl at 257 nm. • Nuclear magnetic resonance: the C=O double-bond exhibits different resonances depending on surrounding atoms, generally a downfield shift. The 13C NMR of a carbonyl carbon is in the range of 160–220 ppm. ==See also==