Look at the following reaction: 1. In the space above, propose a plausible mechanism to yield the product. Remember toshow all arrows for movement of electrons and show any intermediates

that may beformed along the way. You may need to refresh your elementary steps. The reaction in part A has reagents added in two separate steps. What would happen ifboth reagents were added at the same time? Explain your answer. For the reaction below, draw the appropriate arrows to show how the product is formed. The intermediate in this reaction is uncharacteristically stable-so stable that it does notundergo a hydride shift to make a tertiary carbocation. Explain why this intermediate isso stable in the space below.