Mark the correct increasing order of reactivity of the following compounds with $\ce{HBr/HCl}.$
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It is type of nucleophilic substitution reaction followed by $S_N1$ mechanism. $S_N1$ mechanism depends on the stability of carbocation. Presence of electron withdrawing group will decrease the stability of carbocation.
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What is the correct order of reactivity of alcohols in the following reaction?
$\text{R}-\text{OH}+\text{HCL}\xrightarrow{\text{ZnCl}_2}\text{R}-\text{Cl}+\text{H}_2\text{O}$