curry is the simple answer
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.
The formula is C13H10O3
C6h8n2
The phenyl group is uncharged as it is a neutral group with no net charge. Its chemical formula is C6H5, and it consists of a benzene ring with a hydrogen atom removed.
what is the use of phenyl ?
The phenyl is used in the hair care formulations and cosmetics.
Yes, phenyl is a functional group.
Not on its own. It is an aromatic group of atoms with the formula C6H5. One of the carbon atoms in it is bonded to the rest of whatever molecule it is in. The phenyl group is in many aromatic compounds
The condensed structural formula for N-methylaniline is C7H9N, where the nitrogen atom is attached to a methyl group (-CH3) and a phenyl group (-C6H5) on the benzene ring.
The chemical formula of Fipronil is C12H4Cl2F6N4OS.
it has phenyl group to which Mgbr attached at first position
There are lots of polymers, many of which do not contain ring structures. You will need to be more specific as to which polymer you're talking about.One common polymer that does contain rings is polystyrene, in which the rings are simple phenyl rings hanging from a long-chain hydrocarbon backbone. There are also polymers in which the rings are in the backbone, such as poly(ethylene terephthalate) and Kevlar; again, these are phenyl rings in both cases. However, it's certainly possible for there to be rings other than phenyl groups in a polymer.(A phenyl group hanging from the backbone has a formula of C6H5; one that's in the backbone will likely be C6H4, since it needs to connect at two points.)