Organic Chemistry
The most suitable method of separation of $$1 : 1$$ mixture of ortho and para-nitrophenols is:
In the destructive distillation of coal, at 443-503 K temperature, a middle oil or carbolic oil fraction is obtained. This fraction contains :
(3) Distillation of coal tar : Arenes are isolated by fractional distillation of coal tar,
Table :
Name of the fraction
Temperature range (K)
Main constituents
Light oil (or crude oil) fraction
Upto 443
Benzene, toluene, xylene
Middle oil fraction (Carbolic oil)
443-503
Phenol, naphthalene, pyridine
Heavy oil fraction (Creosote oil)
503-543
Naphthalene, naphthol and cresol
Green oil (Anthracene oil)
543-633
Anthracene, phenanthrene
Pitch (left as residue)
Non-volatile
Carbon
So at 443-503 K temperature phenol and naphthalene is formed
Hence options A & C are correct.
The most suitable method of separation of $$1 : 1$$ mixture of ortho and para-nitrophenols is:
What is the difference between distillation, distillation under reduced pressure and steam distillation ?
Explain, why an organic liquid vaporises at a temperature below its boiling point in its steam distillation ?
Those substance which can be separated by steam distillation are:
The boiling points of ethyl acetate and $${CH}_{3}OH$$, respectively are $${77}^{O}C$$ and $${65}^{o}C$$. Which of the following reactions can be shifted to the right by the distillation of the reaction mixture at about $${66}^{o}C$$. $$I. MeCOOEt+MeOH\rightarrow$$ $$II. MeCOOMe+EtOH\rightarrow$$ $$III. MeCOOMe+PhOH\rightarrow$$ $$IV. MeCOOPh+MeOH\rightarrow$$
Aniline is separated from a mixture by:
What is the difference between distillation,distillation under reduced pressure and steam distillation?
Explain, why an organic liquid vaporises at a temperature below its boiling point in its steam distillation ?
A reaction is carried out using aniline as a reactant as well as a solvent. How will you remove unreacted aniline?
How will you separate a mixture of o-nitrophenol and p-nitrophenol?