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Acetophenone on reaction with hydroxylamine can produce two isomeric oximes write structures of oximes?
one of them has the OH group in its right hand butanother has it on the left hand. but i wanna know what is their name
What else can I help you with?
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.
How do you prepare oxime from ketone?
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?
What does an isomerase enzyme do?
As by the name the reaction they catalyse is to change the chemical compound in its isomeric form or we can use isomerase enzymes in transfer of groups within the molecules to yield isomeric frorms.e.gthe enzyme phosphohexose isomerase catalyzes the reversible isomerization of glucose6-phosphate, an aldose to fructose 6-phosphate, a ketone
What is the equation of the reaction between N2H4 and N2O4?
4nh3 + 5o2 --> 4no + 6h2o
What is a stabilizer?
In chemistry, a stabilizer is a chemical that inhibits the reaction between other chemicals. In aerodynamics, stabilizers are structures that produce stability along the horizontal or vertical axis.
What forms from the reaction of bromine with acetophenone?
The reaction of bromine with acetophenone can yield several products, depending on reaction conditions. One common product is α-brominated acetophenone, where bromine adds to the alpha carbon of the carbonyl group. This reaction can also lead to dibrominated acetophenone if excess bromine is used.
Does acetophenone undergo aldol condensation?
Acetophenone can undergo aldol condensation, where it can form a beta-hydroxy ketone through reaction with a strong base. This reaction involves the nucleophilic addition of an enolate ion formed from acetophenone to another acetophenone molecule, followed by dehydration to form the beta-hydroxy ketone product.
How is acetophenone converted into benzoic acid through a specific chemical reaction?
Acetophenone can be converted into benzoic acid through a chemical reaction called oxidation. This reaction involves the use of a strong oxidizing agent, such as potassium permanganate or chromic acid, which adds oxygen atoms to the acetophenone molecule, ultimately forming benzoic acid.
Why you use alcohol in preparation of acetophenone oxime from acetophenone?
Oximes are Compounds containing OH group linked to the nitrogen atom, as we know like dissolves like, so this compound containing OH can be easily dissolved in alcohol, the product will be soluble in alcohol and easy to seperate.\
How do we convert benzene into acetophenone?
To synthesize acetophenone from benzene, you just need to add the aldehyde to the benzene ring. This can be done via a Friedel-Crafts acylation. The reagents are an acid chloride (acetyl chloride in this case) and AlCl3 (stoichiometric).
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.
What is an aminoxylation?
An aminoxylation is an alternative term for a nitrosylation, the reaction of nitric oxide with a biological compound, especially with a sulphur containing part of a protein as a posttranslational modification.
What is the Reaction of cumene and acetyl chloride in the presence of aluminum chloride?
The reaction of cumene with acetyl chloride in the presence of aluminum chloride (AlCl3) is a Friedel-Crafts acylation reaction. This reaction results in the formation of acetophenone as the main product. Aluminum chloride acts as a catalyst in this reaction by facilitating the acylation of cumene.
How do you prepare oxime from ketone?
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?
What does an isomerase enzyme do?
As by the name the reaction they catalyse is to change the chemical compound in its isomeric form or we can use isomerase enzymes in transfer of groups within the molecules to yield isomeric frorms.e.gthe enzyme phosphohexose isomerase catalyzes the reversible isomerization of glucose6-phosphate, an aldose to fructose 6-phosphate, a ketone
What are the structures that provide upward reaction forces?
your stupid and wrong
WHAT ARE STRUCTURES OF MAJOR AND MINOR PRODUCTS OBTAINED WHEN 1-METHYLCYCLOHEXANOL IS DEHYDRATED SING CONC. SULFURIC ACID?
When 1-methylcyclohexanol is dehydrated using concentrated sulfuric acid, the major product formed is 1-methylcyclohexene through an E1 mechanism. Minor products may include 3-methylcyclohexene and other isomeric alkenes due to carbocation rearrangements and side reactions. The reaction conditions and intermediates influence the distribution of products.
