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प्रश्न
Explain the following with an example.
Kolbe’s reaction.
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उत्तर
Phenoxide ion generated by treating phenol with sodium hydroxide is even more reactive than phenol towards electrophilic aromatic substitution. Hence, it undergoes electrophilic substitution with carbon dioxide, a weak electrophile. Ortho hydroxybenzoic acid is formed as the main reaction product.

संबंधित प्रश्न
Write the final product(s) in each of the following reactions:

Write the structures of A, B, C, D and E in the following reactions:

While separating a mixture of ortho and para nitrophenols by steam distillation, name the isomer which will be steam volatile. Give reason.
Write the reaction involved in the following:
Friedal-Crafts Alkylation of Phenol
Picric acid is ____________.
When phenol is treated with excess bromine water, it gives:
When phenol is heated with CHCl3 and alcoholic KOH when salicylaldehyde is produced. This reaction is known as ____________.
On distilling phenol with Zn dust, one gets:
In the reaction of phenol with CHCl3 and aqueous NaOH at 343 K, the electrophile attacking the ring is:
When Phenol is distilled with zinc dust, it gives:

Which of the following species can act as the strongest base?
Phenol does not undergo nucleophilic substitution reaction easily due to ______.
Which of the following are used to convert \[\ce{RCHO}\] into \[\ce{RCH2OH}\]?
(i) \[\ce{H2/Pd}\]
(ii) \[\ce{LiAlH4}\]
(iii) \[\ce{NaBH4}\]
(iv) Reaction with \[\ce{RMgX}\] followed by hydrolysis
Which of the following are benzylic alcohols?
(i) \[\ce{C6H5 - CH2 - CH2OH}\]
(ii) \[\ce{C6H5 - CH2OH}\]
(iii) \[\begin{array}{cc}
\ce{C6H5 - CH - OH}\\
\phantom{}|\phantom{.}\\
\phantom{..}\ce{CH3}\phantom{}
\end{array}\]
(iv) \[\begin{array}{cc}
\ce{C6H5 - CH2 - CH - OH}\\
\phantom{.......}|\phantom{}\\
\phantom{.........}\ce{CH3}\phantom{}
\end{array}\]
Convert the following:
Phenol to N-phenylethanamide.
Which of the following is not aromatic?
How can phenol be prepared from anisole? Give reaction.
Write the name of the reaction, structure and IUPAC name of the product formed when:
Phenol reacts with CHCl3 in the presence of NaOH followed by hydrolysis.
