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Tertiary alkyl halides react much faster via SN1 than SN2, while primary alkyl halides show the opposite trend. Which statement best explains this?

Steric bulk around a tertiary carbon blocks backside nucleophilic attack, while the resulting carbocation is stabilized by hyperconjugation and inductive donation from three alkyl groups.

Tertiary carbons bear more electronegative substituents, which stabilizes the transition state.

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Spair AI: Correct, SN2 needs a clear backside approach to the carbon bearing the leaving group; the three alkyl groups on a tertiary carbon create steric crowding that makes this approach very difficult.

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