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Aryl halides are less reactive towards n...

Aryl halides are less reactive towards nucleophilic substitution reaction. Give four reasons.

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(i) Resonance effect : Haloarenes are resonance stabilized with halogen carbon-double bond. (ii) Hybridization: Carbon in haloarence is sp^2 hybridized which has more s-character and can hold the electron pair of C-X more tightly than sp^3 carbon in haloalkanes. (iii) Instability of phenylcation: Phenylcation is not resonance stabilized.
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SUBHASH PUBLICATION-SUPPLEMENTARY EXAMINIATION QUESTION PAPER JUNE 2017-PART E
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  7. Write equations for the steps in S(N)1 mechanism of conversion of tert...

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  8. Aryl halides are less reactive towards nucleophilic substitution react...

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  9. Write the mechanism of acid catalysed dehydration of ethanol to ethene...

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  10. Explain Reimer-Tiemann reaction.

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  11. Comlete the reaction (i) (ii) (iii)

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  12. Explain Cannizzaro reaction with an example.

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  13. Explain Hoffmann bromamide degradation reaction.

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