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It contains a Secondary Amine group as well as a Secondary Hydroxyl group. There is also a benzene ring which is not considered a functional group.
Polyphenols are determined by a benzene ring containing a carbolic acid (-OH) group. This will be bonded to the ring with an sp hybridized carbon.
I reckon the answer would be that phenol has a hydroxyl group (-OH) which is bonded to a phenyl ring. It yields the same positive result like tyrosine which has a hydroxyl group bonded to its phenyl ring.
the functional group of thymol is phenol because it got an OH group connected to aromatic ring (AR-OH)
Anthranilic acid + ethanol amine C6H4(NH2)COOH + OHCH2CH2NH2 = C6H4(NH2)COOCH2CH2NH2 + H2O Sulphuric acid(H2SO4) is an acid catalyst which deprotonates the carboxylic group(COOH) of anthranilic acid and removes the hydroxy(OH) group from ethanol amine. The (H+) proton then attaches to the (-OH) to form water(H2O) as a byproduct. The deprotonated carboylate(COO-) group of anthranilic acid then attaches to the the (+CH2CH2NH2) to form the amide/ester product. The structure is amine (NH2 bonded to benzene ring) with (COOCH2CH2NH2) bonded to the ortho position of the benzene ring
A Benzene ring and a hydroxl group (-OH).
No. An OH group is not attached to the benzene ring.
OH(hydroxyl) group bonded with a CH2 group attached to benzene ring.
It contains a Secondary Amine group as well as a Secondary Hydroxyl group. There is also a benzene ring which is not considered a functional group.
Polyphenols are determined by a benzene ring containing a carbolic acid (-OH) group. This will be bonded to the ring with an sp hybridized carbon.
It results in maximal alpha and beta receptor activity.
A benzene ring with one -OH.
Phenol is indicated by a benzene ring + -OH group.Fomula for it is C6H6O.
I reckon the answer would be that phenol has a hydroxyl group (-OH) which is bonded to a phenyl ring. It yields the same positive result like tyrosine which has a hydroxyl group bonded to its phenyl ring.
The structural formula for p-xylene is C8H10. It consists of a benzene ring with a methyl group attached to the fourth carbon atom.
There are three deactivating -NO2 groups attached to benzene ring.They reduce electron density of benzene ring very much.So electrons of Oxgen in -OH group attract to benzene ring.Then the negativity of Oxygen reduces.So it is very much easy to break O-H bond and emmit H+.
Each is a completely different molecule. Toluene has a benzene ring with a methyl group attached, Ethanol is a 2 carbon chain with 5 hydrogen atoms and one OH group attached.