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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
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3CH2C(CH3)2CH2I}\]
Name the following halide according to the IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl, or aryl halide:
\[\ce{CH3CH2C(CH3)2CH2I}\]
Give the IUPAC name of the compound.
\[\ce{CICH2 C ≡ CCH2 Br}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides.
\[\ce{CH3CH2C(CH3)2CH2I}\]
Name the following halide according to IUPAC system and classify 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:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Which of the following are secondary bromides?
What should be the correct IUPAC name for diethylbromomethane?
IUPAC name of 
is ______.
Which of the following is an example of vicdihalide?
