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How the following conversion can be carried out? Chloroethane to butane

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प्रश्न

How the following conversion can be carried out?

Chloroethane to butane

रासायनिक समीकरणे/रचना
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उत्तर

\[\ce{\underset{Chloroethane}{2CH3 - CH2 - Cl} + 2Na ->[dry ether, \Delta][Wurtz reaction] \underset{Butane}{CH3 - CH2 - CH2 - CH3} + 2NaCl}\]

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पाठ 6: Haloalkanes and Haloarenes - Exercises [पृष्ठ १९१]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 6 Haloalkanes and Haloarenes
Exercises | Q 6.19 (xvii) | पृष्ठ १९१

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


Explain why Grignard reagents should be prepared under anhydrous conditions?


Write the structure of the major organic product in the following reaction:

\[\ce{C6H5ONa + C2H5Cl ->}\]


How the following conversion can be carried out?

2-Chlorobutane to 3, 4-dimethylhexane


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.


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?


Explain why Grignard reagents should be prepared under anhydrous conditions?


Explain why Grignard reagents should be prepared under anhydrous conditions?


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