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प्रश्न
Why are haloalkanes more reactive towards nucleophilic substitution reactions than haloarenes and vinylic halides?
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 structures of major monohalo products in each of the following reaction:
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:
CH3C(C2H5)2CH2Br
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(Cl)(C2H5)CH2CH3
Which is the correct IUPAC name for \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - Br}\\
\phantom{}|\phantom{.......}\\
\phantom{}\ce{C2H5}\phantom{....}
\end{array}\]?
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 the IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
CH3C(C2H5 )2CH2Br
Write the structure of the following organic halogen compound.
1,4-Dibromobut-2-ene
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
\[\ce{CH_3CH_2C(CH_3)_2CH_2I}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
