Fill in the missing reagents, reactants, or products the synthetic schemes below. Be sure to include any

stereochemical details that you are able to describe. Although it is not important to indicate side products,

indicate all major carbon containing organic products. If specific experimental instructions are necessary to

complete the transformations successfully, indicate in your answers. Assume that all reactions are followed up

with an aqueous work$-$up to neutralize charges.

i$.$

ii$.$

$PhMgBr($excess$)$

$HCl($dilute$)$

Outline an efficient synthesis for the reaction below using the indicated starting material and

any other organic or inorganic reagents necessary