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  2. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group (−C(=O)−OH) [1] attached to an R-group. The general formula of a carboxylic acid is often written as R−COOH or R−CO 2 H , sometimes as R−C(O)OH with R referring to an organyl group (e.g., alkyl , alkenyl , aryl ), or hydrogen , or other groups.

  3. Metal carbonyl - Wikipedia

    en.wikipedia.org/wiki/Metal_carbonyl

    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

  4. Thioketone - Wikipedia

    en.wikipedia.org/wiki/Thioketone

    General formula of a thioketone. In organic chemistry, thioketones (from Ancient Greek θεῖον (theion) 'sulfur'; [1] also known as thiones or thiocarbonyls) are organosulfur compounds related to conventional ketones in which the oxygen has been replaced by a sulfur. [2]

  5. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    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 ...

  6. Dicarbonyl - Wikipedia

    en.wikipedia.org/wiki/Dicarbonyl

    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 ...

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    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 ...

  8. Triruthenium dodecacarbonyl - Wikipedia

    en.wikipedia.org/wiki/Triruthenium_dodecacarbonyl

    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.

  9. Tungsten hexacarbonyl - Wikipedia

    en.wikipedia.org/wiki/Tungsten_hexacarbonyl

    Tungsten hexacarbonyl (also called tungsten carbonyl) is an organometallic compound with the formula W(CO) 6. This complex gave rise to the first example of a dihydrogen complex. [2] Like its chromium and molybdenum analogs, this colorless compound is noteworthy as a volatile, air-stable derivative of tungsten in its zero oxidation state.