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S(N)2 reaction occurs with "inversion of...

`S_(N)2` reaction occurs with `"inversion of configuration" // "racemisation"`.

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To determine whether an \( S_N2 \) reaction results in "inversion of configuration" or "racemization," we can analyze the mechanisms of \( S_N2 \) and \( S_N1 \) reactions step by step. ### Step 1: Understanding \( S_N2 \) Mechanism In an \( S_N2 \) reaction, a nucleophile attacks the electrophilic carbon atom from the opposite side of the leaving group. This backside attack leads to the simultaneous formation of a new bond and the breaking of the old bond. **Hint:** Remember that the nucleophile approaches the carbon atom from the side opposite to the leaving group. ### Step 2: Inversion of Configuration ...
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Out of S_(N^(1)) and S_(N^(2)) which reaction occurs with (a) inversion of configuration (b) racemisation.

(i) Which alkyI hailde from the following pair is chiral and undergoes faster S_(N)2 reaction ? (ii) Out of S_(N)1 and S_(N)2 which reaction occurs with (a) Inversion of configuration (b) Recemisation

Assertion: S_(N)2 reactions proceed with inversion of configuration Reason: S_(N)2 reactions oC Cur in one step .

Assertion:- SN^(2) reaction proceeds with inversion of configuration. Reason:- The attack of nucleophile occurs from a side opposite to the halogen atom resulting in inversion of configuration.

Racemisation occurs in: