State dehydrohalogentation of tert-butyl chloride

Reference no: EM13191905

a) Use the curved arrows to track electron movement in the dehydrohalogentation of tert-butyl chloride by sodium methoxide by the E2 mechanism.

b) Do the same to show the formation of both elimination products from 2-bromo-2methylbutane (page 208 lists the two products as 2-methyl-1-butene and 2-methyl-2-butene.)

Reference no: EM13191905

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