Meta-xylene forms only one trisubstituted benzene (1,2-dimethyle benzene).
Xylene is generally used as a solvent. It is often encountered as a mixture of three different isomers, (same composition different structure), which are generically dimethylbenzenes.Para-xylene (1, 4 dimethyl benzene) can be oxidised toterephthalicacid which is then used for manufacture of PET plastiic.Xylenes can be chlorinated to form disinfectants (PCMX).
Not all plastics but some have, for example Bakelite plastic contains phenols which have the benzene ring. but in free form benzene does not exist in any plastic.
No, it does not
anisole does not form peroxides easily as the oxygen atom is strongly bonded to the benzene ring .
Chloroform is miscible with ethanol, carbon tetrachloride, benzene, diethyil ether etc.
Xylene is generally used as a solvent. It is often encountered as a mixture of three different isomers, (same composition different structure), which are generically dimethylbenzenes.Para-xylene (1, 4 dimethyl benzene) can be oxidised toterephthalicacid which is then used for manufacture of PET plastiic.Xylenes can be chlorinated to form disinfectants (PCMX).
Xylene is generally used as a solvent. It is often encountered as a mixture of three different isomers, (same composition different structure), which are generically dimethylbenzenes.Para-xylene (1, 4 dimethyl benzene) can be oxidised toterephthalicacid which is then used for manufacture of PET plastiic.Xylenes can be chlorinated to form disinfectants (PCMX).
Dibutyl Phathalate Xylene
Ethanol+Water+p-Xylene is an Azeotropic mixture ------------ For p-xylene, zeotropic, but for x-xylene, contradictory results. Please see the links.
The full form of BHC is BENZENE HEXA CHLORIDE.
no
The R(-)-isomer of adrenaline is more potent. Its orientation allows its benzylic hydroyxl to form a hydrogen bond with Serine410 whereas this doesn't happen with S(-)-isomers of adrenaline.
Not all plastics but some have, for example Bakelite plastic contains phenols which have the benzene ring. but in free form benzene does not exist in any plastic.
No benzene is extremely hydrophobic and sits like an oil on top of the water.
A liquid with two layers will form because water is polar and benzene is nonpolar. The two are not miscible.
No, it does not
Benzene has covalent bonds. Each of the six carbons in benzene is sp2 hybridized meaning the ring has both sigma bonds and pi bonds. Benzene is aromatic meaning its pi electrons are delocalized and form a pi system.