Tertiary alkyl halides are practically inert to $SN^2$ mechanism because of....

  • A
    Instability
  • B
    Insolubility
  • C
    Steric hindrance
  • D
    Inductive effect

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Similar Questions

The correct order of $S_N1$ reactivity for the following compounds is:
$(I)$ $CH_3CH_2CH_2CH_2Br$
$(II)$ $CH_2=CH-CH(Br)CH_3$
$(III)$ $CH_3CH_2CH(Br)CH_3$

Chlorination of toluene in the presence of light and heat followed by treatment with aqueous $NaOH$ gives :

Which information below regarding this reaction is applicable?
$CH_3-O-CH_2-Cl \xrightarrow{aq. OH^-, \Delta} CH_3-O-CH_2-OH$

Which alkyl halide has the highest bond enthalpy of the $C-X$ bond?

The $S_{N}2$ reaction mechanism proceeds through ........

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