Advertisements
Advertisements
प्रश्न
How the following conversion can be carried out?
2-Chlorobutane to 3, 4-dimethylhexane
उत्तर
\[\begin{array}{cc}
\ce{2CH3 - CH - CH2CH3 + 2Na ->[dry ether][Wurtz Reaction] CH3CH2 - CH - CH - CH2CH3 + NaCl}\\
|\phantom{..............................................}|\phantom{......}|\phantom{............}\\
\phantom{.}\ce{\underset{2-Chlorobutane}{Cl}\phantom{......................................}\ce{\underset{3, 4-dimethylhexane}{CH3\phantom{...}CH3}\phantom{............}}}\
\end{array}\]
APPEARS IN
संबंधित प्रश्न
How will you bring about the following conversion?
1-Chlorobutane to n-octane
Explain why Grignard reagents should be prepared under anhydrous conditions?
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:
In the preparation of chlorobenzene from aniline, the most suitable reagent is:
A Grignard reagent may be made by reacting magnesium with ____________.
Which one of the following produces acyl halide by treatment with PCl5?
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.
Which of the statements about Grignard reagent is false?
A product (1) of above reaction is:-
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?
