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Predict the predominant alkene product that would form when 2-bromo-2-methylpentane is treated with sodium methoxide in methanol.
Predict the predominant alkene product that would form when 2-bromo-2-methylpentane is treated with sodium methoxide in methanol. If the base were changed to KOC(CH2CH3)3 would the same alkene predominate? If not, why? What would be structure of this alternate product, if it formed?