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Answer:
The increasing order of the reactivity towards SN1 reaction is: II>III>I
Among alkyl halides, the order of reactivity towards the SN1 mechanisms is 3
0
>2
0
>1
0
Here the allyl halide (II) is most reactive towards the SN1 mechanism because reactivity in SN1 reactions depends upon the stability of formed intermediate i.e. carbocation and the formed carbocation of the allyl halide is most stable due to the availability of electrons from the double bond and after that secondary alkyl halide (III) is more stable than primary alkyl halide (I) because of +I-effect of the methyl group.
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