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What happens when bromobenzene is treated with Mg in the presence of dry ether? - Chemistry

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प्रश्न

What happens when bromobenzene is treated with Mg in the presence of dry ether?

रासायनिक समीकरणे/रचना
एका वाक्यात उत्तर

उत्तर

When bromobenzene is treated with Mg in the presence of dry ether, phenylmagnesium bromide is formed.

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पाठ 10: Haloalkanes and Haloarenes - Exercises [पृष्ठ ३१२]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 10 Haloalkanes and Haloarenes
Exercises | Q 22.2 | पृष्ठ ३१२

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:

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


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:
 


A Grignard reagent may be made by reacting magnesium with ____________.


Which of the following alkyl halides is used as a methylating agent?


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).


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


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?


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