answersLogoWhite

0


Best Answer

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?

User Avatar

Wiki User

βˆ™ 16y ago
This answer is:
User Avatar
More answers
User Avatar

AnswerBot

βˆ™ 7mo ago

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.

This answer is:
User Avatar

Add your answer:

Earn +20 pts
Q: How do you prepare oxime from ketone?
Write your answer...
Submit
Still have questions?
magnify glass
imp
Related questions

What is an acetaldoxime?

An acetaldoxime is a chemical compound that belongs to the oxime class of organic compounds. It is derived from the condensation between an aldehyde or ketone and hydroxylamine. Acetaldoximes are often used in organic synthesis and as intermediates in various chemical reactions.


How do you prepare ethyl methyl ketone from calcium acetate?

Ethyl methyl ketone can be prepared from calcium acetate by reacting it with barium hydroxide to form barium acetate, which can then be treated with sulfuric acid to yield ethyl methyl ketone. The ketone can be further purified by distillation.


What is the product of reaction of benzaldehyde with hydroxylamine?

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.


Why glucose penta acetate does not form oxime?

Glucose pentaacetate does not readily form an oxime because the acetyl groups on the glucose molecule hinder the reaction. The acetyl groups create steric hindrance around the reactive carbonyl group, making it difficult for the oxime-forming reaction to occur.


What is an amidoxime?

An amidoxime is an oxime in which one of the substituents (R') is an amino group.


What is the name Ketone with 6 carbons?

methyl ethyl ketone


What is an aldoxime?

An aldoxime is an oxime derived from an aldehyde - with a general formula RCH=NOH.


Is phosgene oxime a vesicant?

Yes, phosgene oxime is a powerful vesicant, which means it causes blistering and tissue damage upon contact with skin or mucous membranes. It was used as a chemical warfare agent in the past due to its blistering properties.


Is cyclohexanone a 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.


What is the difference between litmus strips and ketone strips?

Litmus strips estimate the pH of a solution. Ketone strips detect the presence of ketone bodies in the solution. Specifically, ketone strips are more sensitive for acetoacetate and less so for beta hydroxybutyric acid.


Is ethyl methyl ketone covalent bonded?

The bonds in ethyl methyl ketone are covalent.


What type of molecule is acetone?

ketone