Advertisements
Advertisements
प्रश्न
Write the structure of the major organic product in the following reaction:
\[\ce{C6H5ONa + C2H5Cl ->}\]
उत्तर १
\[\ce{\underset{sodium phenoxide}{C6H5O^-Na} + \underset{ethyl chloride}{C2H5Cl} ->[Williamson Synthesis] \underset{phenetole}{C6H5 - O - C2H5} + NaCl}\]
उत्तर २
Notes
Students can refer to the provided solutions based on their preferred marks.
APPEARS IN
संबंधित प्रश्न
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?
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 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).
Identify the following named reaction:
\[\ce{C2H5Br ->[Na/Dry ether] C2H5 - C2H5}\]
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?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
