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प्रश्न
C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.
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उत्तर
In chlorobenzene, the C−Cl bond gets partial double bond character because of the +M effect shown by the Cl group. Due to double bond character, the bond length decreases in chlorobenzene as compared to the normal CH3−Cl bond length. Therefore, the C–Cl bond length in chlorobenzene is shorter than the C–Cl bond length in CH3–Cl.
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संबंधित प्रश्न
Which would undergo SN1 reaction faster in the following pair and why?

Give reasons for the following:
(CH3)3C–O–CH3 on reaction with HI gives (CH3)3C–I and CH3–OH as the main products and not (CH3)3C–OH and CH3–I.
Write the structures of A, B and C in the following:

Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.
CH3CH2CH2CH2Br or \[\begin{array}{cc}
\ce{CH3CH2CHCH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{Br}\
\end{array}\]
How do polar solvents help in the first step in SN1 mechanism?
Chlorination of alkanes is an example of
Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?
Assertion (A) : Nucleophilic substitution of iodoethane is easier than chloroethane.
Reason (R) : Bond enthalpy of C-I bond is less than that of C-Cl bond.
Retention of configuration is observed in ______.
The compound that will undergo SN1 reaction with the fastest rate is:
