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Select the mechanism(s) that would occur in this reaction and select all the possible products, you may select multiple answe
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Answer #1

Tertiary alkyl halides undergo SN1 reaction to form newly substituted product as tertiary carbocations are more stable than secondary and primary

Tertiary alkyl halides undergo E1 reactions in presence of water or alcohol. If you use strong bases like OH¯ or RO¯, it will undergo E2 reaction

Now the given reaction undergo SN1 reaction and E1 reaction

B product forms by SN1 and E product formed by E1

26) Alkenes undergo epoxidation in presence of mCPBA. In this reaction the stereochemistry will be retained as per the starting material. Cis alkene upon reaction with mCPBA gives cis product and trans alkene gives trans product.

OCH3 oto - CH3OH SNI CH2OH Ε 26. mCPBA

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