Advertisements
Advertisements
Question
Write the structure of the major organic product in the following reaction:
\[\ce{C6H5ONa + C2H5Cl ->}\]
Solution 1
\[\ce{\underset{sodium phenoxide}{C6H5O^-Na} + \underset{ethyl chloride}{C2H5Cl} ->[Williamson Synthesis] \underset{phenetole}{C6H5 - O - C2H5} + NaCl}\]
Solution 2
Notes
Students can refer to the provided solutions based on their preferred marks.
APPEARS IN
RELATED QUESTIONS
How will you bring about the following conversion?
Bromomethane to propanone
Explain why Grignard reagents should be prepared under anhydrous conditions?
What happens when methyl bromide is treated with sodium 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:
In the preparation of chlorobenzene from aniline, the most suitable reagent is:
A Grignard reagent may be made by reacting magnesium with ____________.
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:
\[\ce{C2H5Br ->[Na/Dry ether] C2H5 - C2H5}\]
Reaction of Grignard reagent with aromatic aldehyde and subsequent aqueous treatment produces
\[\ce{R - CH2 - CCl2 - R ->[Peagent] R - C ≅ C - R}\]. The reagent 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?