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Which is incorrect about nucleophilic su...

Which is incorrect about nucleophilic substitution reactions

A

`{:(SN^(1),,SN^(2)),("Favours polar protic solvent",,"Favours polar aprotic solvents"):}`

B

`{:(SN^(1),,SN^(2)),(3^(@) gt 2^(@) gt 1^(@) gt CH_(3)-X("order of reactivity"),,CH_(3)X gt 1^(@) gt 2^(@) gt 3^(@)("order of reactivity")):}`

C

`{:(SN^(1),,SN^(2)),("Two steps",,"One steps"):}`

D

`{:(SN^(1),,SN^(2)),("Inversion of configuration",,"Recemisation with some inversion"):}`

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Assertion: Aryl halides are highly reactive towards nucleophilic substitution reactions. Reason : In case of haloarenes, halogen atom is attached to sp hybridised carbon atom.

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BRILLIANT PUBLICATION-HALOALKANES AND HALOARENES-Level-II
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