Identify the false statement regarding chirality from the following.

  • A
    $S_N1$ reaction yields $1:1$ mixture of both enantiomers.
  • B
    $A$ racemic mixture shows zero optical rotation.
  • C
    Enantiomers are superimposable mirror images of each other.
  • D
    The product obtained by $S_N2$ reaction of haloalkane having chirality at the reactive site shows inversion of configuration.

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In the given reaction
$CH_3-CH(OTs)-CH_2-CH_2-CH(OTs)-CH_3$ $\xrightarrow[(ii) \ KOH]{(i) \ SH^{\ominus} (one \ equivalent)}$ $[X]$
$[X]$ will be :

The order of reactivity of alkyl halides for dehydrohalogenation is:

Predict the order of reactivity of the following compounds in $S_N1$ reaction.
$(I)$ $C_6H_5-CH_2Br$
$(II)$ $C_6H_5-CH(C_6H_5)Br$
$(III)$ $C_6H_5-CH(CH_3)Br$
$(IV)$ $C_6H_5-C(CH_3)(C_6H_5)Br$

Which of the following represents the correct reactivity order for both $SN^1$ and $SN^2$ mechanisms?

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Explain the stereochemistry of $S_{N}1$ reaction with a suitable example.

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