Acetophenone is a specific, aromatic ketone, used in the manufacture of many organic compounds.
Toluene forms from the reaction of bromine with acetophenone.
Acetophenone can be converted into 2-phenyl-2-butanol using a Grignard reagent. Using CH3MgI, the carbonyl group of acetophenone will be attacked by this reagent and yield the alcohol: 2-phenyl-2-propanol.
Yes it does, as it has CH3CO- group.
It is the compound with a benzene ring and propanone
Acetophenone is a specific, aromatic ketone, used in the manufacture of many organic compounds.
Toluene forms from the reaction of bromine with acetophenone.
it is possible to product mannich base using acetophenone with DEA.
Acetophenone is acetyl benzene, acetyl group attached to benzene ring ,C6H5-COCH3
I think you have misunderstood something; Acetophenone is Ph-C=O-CH3, acetylbenzene. It has no isomers so there is no para-acetophenone. Think some more about what you really mean and come back with a refined question.
Acetophenone can be converted into 2-phenyl-2-butanol using a Grignard reagent. Using CH3MgI, the carbonyl group of acetophenone will be attacked by this reagent and yield the alcohol: 2-phenyl-2-propanol.
C6h5c(o)ch3
Yes it does, as it has CH3CO- group.
It is the compound with a benzene ring and propanone
No
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).
Ethyl Acetate