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Why is it that aniline has a high boiling point to phenol and phenol has a high boiling point than toluene and toluene has a high boiling point than benzene?
Wiki User
∙ 9y ago
It s the structure and bonding of Aniline, Phenol, Benzene and Toluene that causes the differences in the boiling points.
Wiki User
∙ 9y ago
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Is phenol an alcohol?
Yes,phenol is an alcohol.It contains a benzene ring and a hydoxile group.
Compound that contains a benzene ring?
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.
How do you convert aniline to phenol?
Use acetic anhydride as reagent. The reaction will undergo nucleophilic addition and the reagent will attach to the amine group. Half of the reagent will become the leaving group and one H of the amine group in the reactant will leave with the reagent. The product will be the benzene ring with an amine, carbonyl, methyl attached.
What is the name of C6H5COOC2H5?
The formula is for benzyl acetate (as an example).
Which one have higher boiling point alcohol or phenol?
Phenol has a higher boiling point than alcohol does; it has a stronger dipole difference in its -OH group.
How will you synthesis of phenol in small scale'?
There are many known syntheses of phenol. However, a few simple ones are: 1) hydrolysis of chlorobenzene: - chlorobenzene + water --> phenol + hydrochloric acid 2) oxidation of toluene: - toluene + oxygen --> phenol + carbon dioxide + water 3) oxidation of benzene with nitrous oxide: - benzene + nitrous oxide --> phenol + nitrogen
Why is o-aniline phenol less soluble in water than m-aniline phenol?
In o-aniline phenol Intramolecular hydrogen bonding occurs which is not possible in meta and is responsible for less solubility
Which is nitrated faster toluene or phenol Explain?
The nitration of phenol is more rapid than that of toluene.
What is more volatile benzene or 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).
Is phenol easier or more difficult to substitute with bromine than benzene?
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.
How do you write phenol?
Phenol is indicated by a benzene ring + -OH group.Fomula for it is C6H6O.
