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प्रश्न
Write the structure of the major organic product in the following reaction:
\[\ce{C6H5ONa + C2H5Cl ->}\]
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उत्तर १
\[\ce{\underset{sodium phenoxide}{C6H5O^-Na} + \underset{ethyl chloride}{C2H5Cl} ->[Williamson Synthesis] \underset{phenetole}{C_6H_5 - O - C_2H_5} + NaCl}\]
उत्तर २
संबंधित प्रश्न
What happens when methyl bromide is treated with sodium in the presence of dry ether?
In the preparation of chlorobenzene from aniline, the most suitable reagent is:
What would be the reactant and reagent used to obtain 2, 4-dimethyl pentan-3-ol?
Which of the following statements are correct about the reaction intermediate?
(i) Intermediate (c) is unstable because in this carbon is attached to 5 atoms.
(ii) Intermediate (c) is unstable because carbon atom is sp2 hybridised.
(iii) Intermediate (c) is stable because carbon atom is sp2 hybridised.
(iv) Intermediate (c) is less stable than the reactant (b).
Draw other resonance structures related to the following structure and find out whether the functional group present in the molecule is ortho, para directing or meta directing.
Identify the following named reaction:
\[\ce{C2H5Br ->[Na/Dry ether] C2H5 - C2H5}\]
Which of the statements about Grignard reagent is false?
\[\ce{R - CH2 - CCl2 - R ->[Peagent] R - C ≅ C - R}\]. The reagent is:-
A product (1) of above reaction is:-
Explain why Grignard reagents should be prepared under anhydrous conditions.
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
