The target alkyl halide used can easily be prepared by adding $HBr$ to the intermediate alkene in a

Markovnikov fashion.

Perform the following syntheses. Use the retrosynthetic analysis shown in the example. Be

certain to show all of your reasoning which leads to your final answer. Both can be accomplished

in $2-3$ steps. Show all reagents and intermediate products. All reactions necessary to complete

these syntheses can be found in Chapters $6,7,$ and $9.$ Also, look at the reactions in Part I.

Remember, start from the target product and go one$-$step back to get started.