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.
Benzene has a lower boiling point than toluene because it has weaker intermoleclar forces. Benzene has a higher melting point than toluene because it is more symmetrical.
The nitration of phenol is more rapid than that of toluene.
Yes. The methyl group on toluene causes a shift in electron density making it polar. Benzene is non-polar and has uniform distribution of charge density and has no dipole moment. Toluene, though, would not be more polar than a phenol because the more electronegative oxygen atom (in the alcohol) pulls more electron density from the ring causing a larger dipole moment (separation of charge).
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.
Yes, ethyl acetate is more polar than toluene.
because nitro group is ring deactivating group, nitration of nitro benzene is more difficult than benzene.
Benzene has a lower boiling point than toluene because it has weaker intermoleclar forces. Benzene has a higher melting point than toluene because it is more symmetrical.
Less than 0.01%
The nitration of phenol is more rapid than that of toluene.
It s the structure and bonding of Aniline, Phenol, Benzene and Toluene that causes the differences in the boiling points.
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+
Yes. The methyl group on toluene causes a shift in electron density making it polar. Benzene is non-polar and has uniform distribution of charge density and has no dipole moment. Toluene, though, would not be more polar than a phenol because the more electronegative oxygen atom (in the alcohol) pulls more electron density from the ring causing a larger dipole moment (separation of charge).
Examples: ethanol, methanol, benzene, cyclohexane, toluene, etc.
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.
Benzene is an organic molecule made up of six carbon atoms connected to form a ring. This is called the benzene ring. The benzene ring structure occures in several other, more complex, organic moleculed.
Benzene has a stable structure. Aspirin has an carboxylic group with delocalized electrons. So aspirin is more reactive than benzene.
Yes, ethyl acetate is more polar than toluene.