Since there is intramolecular hydrogen bonding between -OH and -NO2 groups, present in the ORTHO-nitrophenol (they are very close to each other), these ortho-molecules do NOT attrack each other so much by intermolecular forces caused by hydrogen bonding as is the case with meta- and para-nitrophenol.
Phenol is flammable.
What are some examples of Phenol
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Both water and phenol are very weak acids. Though phenol is the stronger of the two.
Any phenol that has substituents in a 1, 3 configuration.
Phenol is flammable.
by steam distillation as o-nitrophenol is volatile due to intra-molecular hydrogen bonding, SYNCRO, GKP
phenol
phenol
This is because the two isomers have different boiling points and one of which falls under 100 degrees celsius (2-nitrophenol). hence the first to evaporate out is the 2nitrophenol and the rest will be 4nitrophenol. This is because the two isomers have different boiling points and one of which falls under 100 degrees celsius (2-nitrophenol). hence the first to evaporate out is the 2nitrophenol and the rest will be 4nitrophenol.
What are some examples of Phenol
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Both water and phenol are very weak acids. Though phenol is the stronger of the two.
Phenol. Phenol's Dipole Moment: 1.7D Phenyl chloride's Dipole Moment: 1.54D
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.
phenol is used as a odor eliminator
Any phenol that has substituents in a 1, 3 configuration.