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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
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?
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.
Why is it necessary to avoid even traces of moisture during the use of a Grignard reagent?
Identify the following named reaction:
\[\ce{C2H5Br ->[Na/Dry ether] C2H5 - C2H5}\]
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?
