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प्रश्न
How will you bring about the following conversion?
1-Chlorobutane to n-octane
How will you bring about the following conversion in not more than two steps?
1-Chlorobutane to n-octane
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उत्तर
\[\ce{\underset{1-Chlorobutane}{2CH3CH2CH2CH2Cl} + 2Na ->[dry ether][Wurtz reaction] \underset{n-octane}{CH3CH2CH2CH2 - CH2CH2CH2CH3} + 2NaCl}\]
संबंधित प्रश्न
How will you bring about the following conversion?
Bromomethane to propanone
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 one of the following produces acyl halide by treatment with PCl5?
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).
Why is it necessary to avoid even traces of moisture during the use of a Grignard reagent?
Identify the following named reaction:
\[\ce{C2H5Br ->[Na/Dry ether] C2H5 - C2H5}\]
\[\ce{R - CH2 - CCl2 - R ->[Peagent] R - C ≅ C - R}\]. 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?
Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
