Tertiary alkyl halides show SN1 reactions mostly Why?
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Ответ:
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.
Ответ:
42.98 g/L
Explanation: