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प्रश्न
Why are haloalkanes more reactive towards nucleophilic substitution reactions than haloarenes and vinylic halides?
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उत्तर
Haloalkanes are more reactive than haloarenes and vinylic halides because of the presence of a partial double bond character C-X bond in haloarenes and vinylic halides. Hence they do not undergo nucleophilic reactions easily.
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संबंधित प्रश्न
Draw the structure of major monohalo products in the following reaction:
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3CH = CHC(Br)(CH3)2
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
o-Br-C6H4CH(CH3)CH2CH3
Identify the compound Y in the following reaction.
What should be the correct IUPAC name for diethylbromomethane?
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3CH2 C(CH3)2CH2I}\]
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(Cl)(C2H5)CH2CH3
Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
