React aniline with HCl/NaNO2 (diazotisation) followed by reaction with KOH to give phenol. Nitration of phenol with fuming nitric acid gives picric acid (or trinitrophenol).
Yes. Two isomers of toluene are known as toluene-2,4-diisocyanate and toluene-2,6-diisocyanate
Toluene is not miscible with water; toluene is released by slow evaporation.
Toluene is an aromatic compound.
Mineral oils don't contain aniline, but the aniline pointis a characteristic of oils (defining the content of aromatic hydrocarbons).
yeah
It s the structure and bonding of Aniline, Phenol, Benzene and Toluene that causes the differences in the boiling points.
aniline would go through an electrophilic substitution, it is a weak base
From what the internet shows, you convert toluene into nitro-toluene, not the other way around. Further, the reagents used to do that are generally things that will allow the toluene to oxidize.
by using kMNo4 and water
React aniline with HCl/NaNO2 (diazotisation) followed by reaction with KOH to give phenol. Nitration of phenol with fuming nitric acid gives picric acid (or trinitrophenol).
Toluene had heat of vaporization of 38.06 kJ/mol Toluene molecular mass is 92.14 g/mol You just need to convert heat of vaporization into kJ/g basis and multiply your 5 gram to get the required amount of heat.
There is no any such difference between Aniline point and mixed Aniline point . . . . .
Yes. Two isomers of toluene are known as toluene-2,4-diisocyanate and toluene-2,6-diisocyanate
C6H5CH3 is toluene.
What is the pH of toluene?
Toluene is not miscible with water; toluene is released by slow evaporation.