5. Propose a synthesis for the following product from the starting material(s) indicated. Show all reagents and products of each step of your sequence. Show retrosynthetic analysis. OH OH O Ph

Propose a synthesis from the reagents below

Propose a synthesis for the following product from the starting material(s) indicated. Show all reagents and products of each step of your sequence. Show retrosynthetic analysis. фон OH OH

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Propose a synthesis for the following compound.

Show how you could accomplish the following transformation. Be sure to show the structures of the products after each reaction you propose as well as the reagents required for each reaction. You do not need to show reaction mechanisms or a retrosynthesis.

Propose a sequence of reactions to prepare the specified target compound from the indicated starting materials.  All of the carbon atoms in the target must originate in the specified starting materials.  Keeping this restriction in mind, you may use any other organic or inorganic reagents necessary to complete the synthesis. It is only necessary to show the overall transformations involved in your proposed synthesis.

Propose a synthetic method to hydrate but-1-ene, which will yield the product opposite of 2-butanol

Show the product of each synthetic step. Draw mechanisms. Ph OH 1) NaH, then coa Br 2) DIBAH, then aq. workup 3) Ph₂P=CH₂ Ph 2 Grubbs catalyst Ph 3

Propose a retrosynthetic analysis of benzocaine from the starting material shown. Your answer should include both the synthons and the reagents that would be employed in the actual synthesis. H2N