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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
\[\ce{\underset{sodium phenoxide}{C6H5O^-Na} + \underset{ethyl chloride}{C2H5Cl} ->[Williamson Synthesis] \underset{phenetole}{C6H5 - O - C2H5} + NaCl}\]
उत्तर २
संबंधित प्रश्न
Identify A, B, C, D, E, R and R1 in the following:
How will you bring about the following conversion?
Bromomethane to propanone
How will you bring about the following conversion?
1-Chlorobutane to n-octane
What happens when bromobenzene is treated with Mg in the presence of dry ether?
How the following conversion can be carried out?
2-Chlorobutane to 3, 4-dimethylhexane
Write the structure of main compounds A and B in the following reaction:
Which of the following alkyl halides is used as a methylating agent?
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).
Reaction of Grignard reagent with aromatic aldehyde and subsequent aqueous treatment produces
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:-
Grignard reagent shows addition on
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?
