Advertisements
Advertisements
Question
You are given benzene, conc. H2SO4 and NaOH. Write the equations for the preparation of phenol using these reagents.
Advertisements
Solution 1

Solution 2
\[\ce{\underset{Benzene}{C6H6} ->[conc.H2SO4/ \Delta][sulfonation] \underset{Benzene sulphonic acid}{C6H5SO3H} ->[NaOH, melting][-Na2SO3] \underset{Sodium phenoxide}{C6H5ONa} ->[Dil. HCl][-NaCl] \underset{Phenol}{C6H5OH}}\]
APPEARS IN
RELATED QUESTIONS
Give the equations of reactions for the preparation of phenol from cumene.
Write chemical reaction for the preparation of phenol from chlorobenzene.
Write the structures of main products when benzene diazonium chloride (C6 H5 N+2CI−)C6 H5 N2+CI- reacts with the :Cu/HBr
What happens when Phenol is oxidised with Na2Cr2O7/H+?
Why phenol undergoes electrophilic substitution more easily than benzene?
Sodium salt of benzene sulphonic acid on fusion with caustic soda gives ____________.
Which of the following will not form phenol or phenoxide?
Which of the following reactions will yield phenol?
| (i) | ![]() |
| (ii) | ![]() |
| (iii) | ![]() |
| (iv) | ![]() |
Name the starting material used in the industrial preparation of phenol.
What happens when reactions:
N-ethylethanamine reacts with benzenesulphonyl chloride.
Benzoic acid reacts with cone. HNO3 and HiSO4 to give:
Oxidation of which of the following by air in presence of vanadium pent oxide given phenol?
Aspirin is also known as
In the reaction, alcohol + diazomethane → ether + N2; the ether cannot be ______.

Consider the above reactions, the product A and product B respectively are:
'A' and 'B' in the following reactions are:





