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Provide a complete curved-arrow mechanism for the following transformation (10 points) CI Cl
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CI CI Non-benzylic carbocation CI Cl i.e CI Benzylic Carbocation Benzylic Carbocation Thermal rearrangement. Cl departs and gives a non-benzylic hence less stable carbocation. Then S with lone pair stabilizes the structure through cyclic sulphonium ion. which eventually breaks into a benzylic and hence very stable carbocation. This benzylic carbocation then atacked by Cand gives the product.

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