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$\mathrm{SN}^1$ reaction is feasible in(a)-(d) Structure can't copy
Step 1
SN1 reactions proceed through a carbocation intermediate, so they are favored when: - The substrate can form a stable carbocation - The leaving group is good (easily departs) - The solvent is polar protic (helps stabilize the leaving group) Show more…
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$\mathrm{SN}^{1}$ reaction is feasible in
$\mathrm{SN}^{1}$ reaction is feasible in (a) $\rightarrow \mathrm{Cl}+\mathrm{KOH}$ (b) $\mathrm{Cl}+\mathrm{KOH}$ (c) <smiles>CNC(=O)c1ccccc1</smiles> (d)
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