because nitro group is ring deactivating group, nitration of nitro benzene is more difficult than benzene.
The resonance structure of nitrobenzene helps stabilize the molecule, making it less reactive than benzene. This stability affects its chemical properties by reducing its tendency to undergo certain reactions, such as electrophilic aromatic substitution.
So that only one NO2+ is substituted for the hydrogen on one of the carbons in benzene , if it was above 50 degree Celsius then more than one hydrogen would be substituted and mono nitration is only one substitution of hydrogen for NO2+
Phenol and benzene are both aromatic compounds, but phenol has a hydroxyl group (-OH) attached to the benzene ring, making it more reactive than benzene. Phenol can undergo reactions such as oxidation and substitution more readily than benzene. Additionally, phenol is more acidic than benzene due to the presence of the hydroxyl group.
Kerosene and benzene can be separated by fractional distillation. Since benzene has a lower boiling point than kerosene, the mixture can be heated to vaporize the benzene, which is then collected as a separate fraction.
Chlorobenzene is more polar than benzene because it has a chlorine atom attached to the benzene ring, which induces a dipole moment and increases its overall polarity compared to benzene.
Hi ,As you know from the structures of both the compounds that toluene has a methyl group on the benzene ring which is electron releasing group and hence activate the benzene ring by pushing the elctrons on the benzene ring. On the other hand nitro group on the benzene ring is electron withdrawing group which deactivates the benzene ring by withdrawing the electrons from the benzene ring . Now in the nitration attack of the nucleophile ( NO2 +) takes place. Hence reaction will takes place on that benzene faster which have more electron density on its ring which is the case of toluene.
The resonance structure of nitrobenzene helps stabilize the molecule, making it less reactive than benzene. This stability affects its chemical properties by reducing its tendency to undergo certain reactions, such as electrophilic aromatic substitution.
So that only one NO2+ is substituted for the hydrogen on one of the carbons in benzene , if it was above 50 degree Celsius then more than one hydrogen would be substituted and mono nitration is only one substitution of hydrogen for NO2+
The substitution reactions of phenol are easier than benzene, phenol directly reacts with bromine and gives tribromo phenol while benzene requires FeCl3 as a catalyst and gives mono bromo phenol.
The vapor pressure of nitrobenzene at its boiling point (210.9°C) is equal to the atmospheric pressure, which is 1 atm. At 102°C, the vapor pressure of nitrobenzene would be lower than 1 atm, as the boiling point is higher than 102°C.
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.
Benzene has a stable structure. Aspirin has an carboxylic group with delocalized electrons. So aspirin is more reactive than benzene.
Phenol and benzene are both aromatic compounds, but phenol has a hydroxyl group (-OH) attached to the benzene ring, making it more reactive than benzene. Phenol can undergo reactions such as oxidation and substitution more readily than benzene. Additionally, phenol is more acidic than benzene due to the presence of the hydroxyl group.
Kerosene and benzene can be separated by fractional distillation. Since benzene has a lower boiling point than kerosene, the mixture can be heated to vaporize the benzene, which is then collected as a separate fraction.
Chlorobenzene is more polar than benzene because it has a chlorine atom attached to the benzene ring, which induces a dipole moment and increases its overall polarity compared to benzene.
Benzene is less dense than water, so it will float on top of water, making it the upper layer in this case.
Benzene has a lower boiling point than toluene because it has a symmetric structure that experiences weaker van der Waals forces, making it easier for benzene molecules to separate and vaporize. The higher melting point of benzene compared to toluene is due to the presence of delocalized electron cloud in benzene, which results in stronger intermolecular interactions (π-π interactions) between benzene molecules in the solid state.