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Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone ( >C=O ). It is a colorless, highly volatile , and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops .
Structure and properties Index of refraction, n D: 1.3561 Dielectric constant, ... Vapor pressure of acetone based on formula, = + from ...
The chemistry symbols of this structural formula are drawn using the path text method. This SVG structural formula shows a very simple image. Drawing uncomplicated graphics with a text editor seems more adequate than using a vector graphics program, and will often result in a dramatic reduction of file size.
In organic chemistry, a ketone / ˈ k iː t oʊ n / is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO ...
Acetone peroxide (/ æ s ə ˈ t ə ʊ n p ɛr ˈ ɒ k s aɪ d / ⓘ also called APEX and mother of Satan [3] [4]) is an organic peroxide and a primary explosive. It is produced by the reaction of acetone and hydrogen peroxide to yield a mixture of linear monomer and cyclic dimer , trimer , and tetramer forms.
General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]
The structure of the acetylacetonate anion (acac −) In the acetylacetonate anion, both C-O bonds are equivalent. Both C-C central bonds are equivalent as well, with one hydrogen atom bonded to the central carbon atom (the C3 atom).
Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate: