Provide a multistep synthesis for ONE of the two problems below. You get to choose. Note that each carbon in
your final product must originate from the given starting material. You have an infinite supply of
that starting material. You also have an infinite supply of anything you make from it. You can use
any other reagents you want, and you do not have to make them yourself, as long as they do not
become part of your final product structure. For example, if you use CH3CH2O (ethoxide) as a strong base for an E2, you do not have to make it. If you use it as a nucleophile for SN2 and it
becomes part of your product, then you do have to make it. You are not asked to provide any arrow-pushing mechanisms. You are not required to show a retrosynthetic analysis. At a minimum provide a correct sequence of reactions even without showing any products along the way. Include synthetic intermediates, which are just the products made along the way, whether as part of a retrosynthesis or forward synthesis.
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