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carbonyl group |
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carbonyl group (kär`bənĭl), in chemistry, functional group functional group, in organic chemistry, group of atoms within a molecule that is responsible for certain properties of the molecule and reactions in which it takes part. ..... Click the link for more information. that consists of an oxygen atom joined by a double bond to a carbon atom. The carbon atom is joined to the remainder of the molecule by two single bonds or one double bond. If the carbonyl group is joined only to alkyl groups alkyl group (ăl`kĭl), in chemistry, group of carbon and hydrogen atoms derived from an alkane molecule by removing one hydrogen atom ..... Click the link for more information. or aryl groups aryl group (âr`ĭl), in chemistry, group of atoms derived from benzene or from a benzene derivative by removing one hydrogen that is ..... Click the link for more information. , the compound is a ketone ketone (kē`tōn), any of a class of organic compounds that contain the carbonyl group , C=O, and in which the carbonyl group is ..... Click the link for more information. ; if it is joined to at least one hydrogen atom, the compound is an aldehyde aldehyde (ăl`dəhīd) [alcohol + New Lat. ..... Click the link for more information. . The chemical reactivity of aldehydes and ketones is primarily due to the difference in electronegativity electronegativity (ĭlĕk'trōnĕgətĭv`ətē) ..... Click the link for more information. between carbon and oxygen. Because oxygen has the greater affinity for electrons, it acquires a partial negative charge, becoming electron-rich; the carbon atom of the carbonyl group thus becomes electron-deficient, acquiring a partial positive charge. One major type of reaction of aldehydes and ketones involves the addition of an electron-rich chemical species to the electron-deficient carbon atom of the carbonyl group. Another type of reaction is due to the tendency of the electron-deficient carbon atom of the carbonyl group to partially attract electrons from carbon atoms adjacent to it in the molecule, thus increasing the acidity of hydrogen atoms that are bonded to the adjacent carbon. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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The aromatic C-H wag is also affected by the carbonyl group and shifted down to 723 [cm. In contrast, its analogue, mirex, which has the carbonyl group replaced by two chlorine atoms, is inactive in binding. Most of the protected hydrogen atoms were involved in hydrogen bonds with main-chain carbonyl groups especially those that were part of the secondary structure. |
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