$(+)-2-$chloro$-2-$phenylethane in toluene racemises slowly in the presence of small amount of $SbCl_5$, due to the formation of

  • A
    carbanion
  • B
    carbene
  • C
    free-radical
  • D
    carbocation

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Consider the reaction: $CH_3-CH_2-CH(F)-CH_3 \xrightarrow{CH_3O^{-}} X$. The alkene formed in major amount is:

Arrange the following in order of ease of dehydrohalogenation:
$(i)$ Bromocyclohexane
(ii) $3-$Bromocyclohexene
(iii) $3-$Bromocyclohexa$-1,4-$diene
(iv) Bromobenzene

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Which compound in each of the following pairs will react faster in $S_N2$ reaction with $OH^{-}$?
$(i)$ $CH_3-Br$ or $CH_3-I$
$(ii)$ $CH_3-C(CH_3)_2-Cl$ or $CH_3-Cl$

In the alkaline hydrolysis of a tertiary alkyl halide by aqueous alkali,if the concentration of the alkali is doubled,then the reaction rate:

Which of the following factors favors an $S_N1$ reaction?

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