Why tertiary alkyl halides undergoes SN1
reaction
very
fast ?
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Answer:
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Explanation:
Generally SN1 reactions are carried out in polar protic solvents. The energy required for breaking the C-X bond is obtained through solvation of halide ion with the proton of the solvent. Tertiary alkyl halides undergo SN1 reaction very fast because of the high stability of tertiary carbocations.
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