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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
Identify A, B, C, D, E, R and R1 in the following:
How will you bring about the following conversion?
1-Chlorobutane to n-octane
How the following conversion can be carried out?
Chloroethane to butane
Write the structure of main compounds A and B in the following reaction:
A Grignard reagent may be made by reacting magnesium with ____________.
Which of the following alkyl halides is used as a methylating agent?
Which one of the following produces acyl halide by treatment with PCl5?
\[\ce{R - CH2 - CCl2 - R ->[Peagent] R - C ≅ C - R}\]. The reagent is:-
Grignard reagent shows addition on
The product formed in the first step of the reaction
\[\begin{array}{cc}
\ce{Br}\phantom{......}\\
|\phantom{.......}\\
\ce{CH3-CH2-CH-CH2-CH-CH3}\\
\phantom{...............}|\\
\phantom{................}\ce{Br}
\end{array}\]
with excess Mg/Et2O(Et = C2H5) 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?
