Examine the following statements pertaining to an $S_N2$ reaction:
$(1)$ The rate of reaction is independent of the concentration of the nucleophile.
$(2)$ The nucleophile attacks the $C$ atom on the side of the molecule opposite to the group being displaced.
$(3)$ The reaction proceeds with simultaneous bond formation and bond rupture/cleavage.
Amongst the following,which of the above are true?

  • A
    $1, 2$
  • B
    $1, 3$
  • C
    $1, 2, 3$
  • D
    $2, 3$

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Similar Questions

Given below are two statements:
Statement $(I)$: Benzyl chloride reacts faster in $S_N1$ mechanism than ethyl chloride.
Statement $(II)$: Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.
In the light of the above statements, choose the correct answer from the options given below:

Arrange the following halides in decreasing order of $S_N1$ reactivity:
$(I)$ $CH_3CH_2CH_2Cl$
$(II)$ $CH_2=CHCHClCH_3$
$(III)$ $CH_3CH_2CHClCH_3$

Which among the following metals is involved in the preparation of a Grignard reagent?

Isopropyl chloride undergoes hydrolysis by which mechanism?

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Which one of the following will be most reactive for $SN^1$ reaction?

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