http://wiki.answers.com/Q/How_do_you_prepare_oxime_from_ketone in high yield and separate its isomers? http://wiki.answers.com/Q/How_do_you_prepare_oxime_from_ketone in high yield and separate its isomers?
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Oximes can be prepared from ketones by reacting the ketone with hydroxylamine under acidic conditions. The hydroxylamine reacts with the ketone to form the oxime through a nucleophilic addition reaction. The resulting oxime can then be isolated through extraction and purification steps.
Benzaldehyde and hydroxylamine will produce oxime ethers. Oxime is any of a class of organic compounds, of general formula RR'C=NOH, derived from the condensation of an aldehyde (R' = H) or ketone with hydroxylamine.
methyl ethyl ketone
Yes, cyclohexanone is a ketone. It is a cyclic ketone with a six-membered carbon ring and a carbonyl group attached to one of the carbon atoms in the ring.
The bonds in ethyl methyl ketone are covalent.
No, fructose is a monosaccharide sugar that is classified as a ketohexose. It contains a ketone functional group in its structure.