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  2. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    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' are methyl), with the formula (CH 3) 2 CO ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, (CH 3) 2 CHCH 2 CH 3 (isopentane) is named 2-methylbutane, not 3-methylbutane. If there are multiple side-branches of the same size alkyl group, their positions are separated by commas and the group prefixed with multiplier prefixes depending on the number of branches. For example, C(CH 3) 4 (neopentane) is named 2,2 ...

  4. Category:Ketone solvents - Wikipedia

    en.wikipedia.org/wiki/Category:Ketone_solvents

    Pages in category "Ketone solvents" The following 14 pages are in this category, out of 14 total. This list may not reflect recent changes. A. Acetone; Acetophenone; B.

  5. Enol - Wikipedia

    en.wikipedia.org/wiki/Enol

    A classic example for favoring the keto form can be seen in the equilibrium between vinyl alcohol and acetaldehyde (K = [enol]/[keto] ≈ 3 × 10 −7). In 1,3-diketones, such as acetylacetone (2,4-pentanedione), the enol form is more favored. The acid-catalyzed conversion of an enol to the keto form proceeds by proton transfer from O to carbon.

  6. Category:Ketones - Wikipedia

    en.wikipedia.org/wiki/Category:Ketones

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  7. Locant - Wikipedia

    en.wikipedia.org/wiki/Locant

    For example, there are at least two isomers of the linear form of pentanone, a ketone that contains a chain of exactly five carbon atoms. There is an oxygen atom bonded to one of the middle three carbons (if it were bonded to an end carbon, the molecule would be an aldehyde , not a ketone), but it is not clear where it is located.

  8. Ketone halogenation - Wikipedia

    en.wikipedia.org/wiki/Ketone_halogenation

    The position alpha to the carbonyl group (C=O) in a ketone is easily halogenated. This is due to its ability to form an enolate (C=C−O −) in basic solution, or an enol (C=C−OH) in acidic solution. An example of alpha halogenation is the mono-bromination of acetone ((CH 3) 2 C=O), carried out under either acidic or basic conditions, to ...

  9. Ketogenesis - Wikipedia

    en.wikipedia.org/wiki/Ketogenesis

    The result is a rate of ketone production higher than the rate of ketone disposal, and a decrease in blood pH. [12] In extreme cases the resulting acetone can be detected in the patient's breath as a faint, sweet odor. There are some health benefits to ketone bodies and ketogenesis as well.