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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 the major monohalo product in the following reaction:
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3CH = C(Cl)CH2CH(CH3)2
Ethylidene chloride is a/an ______.
What should be the correct IUPAC name for diethylbromomethane?
Haloalkanes contain halogen atom (s) attached to the sp3 hybridised carbon atom of an alkyl group. Identify haloalkane from the following compounds.
(i) 2-Bromopentane
(ii) Vinyl chloride (chloroethene)
(iii) 2-chloroacetophenone
(iv) Trichloromethane
Which of the following compounds can be classified as aryl halides?
(i) \[\ce{p-ClC6H4CH2CH(CH3)2}\]
(ii) \[\ce{p-CH3CHCl(C6H4)CH2CH3}\]
(iii) \[\ce{o-BrH2C - C6H4CH(CH3)CH2CH3}\]
(iv) \[\ce{C6H5 - Cl}\]
Which alkyl halide has maximum density
Name the following halide according to the IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl, or aryl halide:
\[\ce{CH3CH2C(CH3)2CH2I}\]
Write the structure of the following organic halogen compound.
1,4-Dibromobut-2-ene
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
