when 1-methoxy-2-methylpropene is treated with HCI, the major product is 1-chlora-1-methoxy-2-methylpropane. Although this reaction proceeds via an ionic mechanism, the Cl is ultimately positioned at the less substituted carbon. Draw a mechanism that is consistent with this outcome. Do not put reagent(s) above the arrow. 1 -methoxy-2-methylpropane -Chloro- 1-Methoxy-2-methylpropene