2-nitro toluene may under go electrophilic substitution reactions as Nitration, Halogenation at 4th position.
The molecular diameter of toluene is approximately 0.6 to 0.7 nanometers (nm). This value can vary slightly depending on the method of measurement and the specific conditions, but it generally reflects the size of the toluene molecule, which consists of a benzene ring with a methyl group. Toluene's relatively small size allows it to easily participate in various chemical reactions and interactions.
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.
Each of silicon and platinum is an element, but toluene is not.
Electrophilic halogenation
The molecular diameter of toluene is approximately 0.6 to 0.7 nanometers (nm). This value can vary slightly depending on the method of measurement and the specific conditions, but it generally reflects the size of the toluene molecule, which consists of a benzene ring with a methyl group. Toluene's relatively small size allows it to easily participate in various chemical reactions and interactions.
aniline would go through an electrophilic substitution, it is a weak base
Yes. Two isomers of toluene are known as toluene-2,4-diisocyanate and toluene-2,6-diisocyanate
C6H5CH3 is toluene.
Toluene is not miscible with water; toluene is released by slow evaporation.
Toluene is an aromatic compound.
Phenol is nitrated faster than toluene because phenol is more reactive towards electrophilic aromatic substitution reactions due to the presence of the hydroxyl group (-OH) which activates the benzene ring by donating electrons to it. This increases the electron density on the ring and makes it more susceptible to electrophilic attack by the nitronium ion in nitration reactions.
toluene is a common name - The IUPAC name for toluene is methylbenzene.
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.
Neither. Toluene is a compound.
No it is not soluble in toluene because toluene is nonpolar and nacl is polar