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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 ...
Remarkably, ketone halogenation also occurs in biological systems, particularly in marine algae, where dibromoacetaldehyde, bromoacetone, 1, l,l -tribromoacetone, and other related compounds have been found. The halogenation is a typical α-substitution reaction that proceeds by acid catalyzed formation of an enol intermediate. [1]: 846
However, a mixed acid-base disorder may be present especially if vomiting is contributing to a hypochloremic alkalosis. [2] The ketone which is present is mostly beta-hydroxybutyrate rather than acetoacetate resulting in only a weakly positive nitroprusside test. [2] People usually do not present with high blood sugar or sugar in the urine. [2]
In organic chemistry, aldol reactions are acid- or base-catalyzed reactions of aldehydes or ketones. Aldol addition or aldolization refers to the addition of an enolate or enolation as a nucleophile to a carbonyl moiety as an electrophile. This produces a β-hydroxyaldehyde or β-hydroxyketone.
The accumulation of acetyl-CoA in turn produces excess ketone bodies through ketogenesis. [11] 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.
While the traditional Meyer–Schuster rearrangement uses harsh conditions with a strong acid as the catalyst, this introduces competition with the Rupe reaction if the alcohol is tertiary. [2] Milder conditions have been used successfully with transition metal -based and Lewis acid catalysts (for example, Ru- [ 11 ] and Ag-based [ 12 ] catalysts).
Blood tests for the diagnosis of diabetic ketoacidosis measure glycemia (sugar level), pH (blood acidity), and ketone bodies. As urgent medical treatment is often required when DKA is suspected, the tentative diagnosis can be made based on clinical history and by calculating the anion gap from the basic metabolic panel , which would demonstrate ...
The Kornblum–DeLaMare rearrangement is a rearrangement reaction in organic chemistry in which a primary or secondary organic peroxide is converted to the corresponding ketone and alcohol under acid or base catalysis. The reaction is relevant as a tool in organic synthesis and is a key step in the biosynthesis of prostaglandins. [1]