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प्रश्न
Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.
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उत्तर
- The presence of electron-withdrawing (–NO2) group at ortho and para position greatly increases the reactivity of 2, 4-dinitrochlorobenzene towards substitution of halogen atom.
- Greater the number of electron-withdrawing (–NO2) groups at o and p position, greater is the reactivity. Therefore, nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene.
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संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
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\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]
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Observe the following and answer the question given below:
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Observe the following and answer the question given below:
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Identify the chiral molecule from the following.
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Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
