In order to synthesis 1-phenylbutan-1-ol, you started the reaction with a hydration of prop-1-ene using the hydroboration method. Then you oxidized the intermediate with KMNO4. Finally, alkylation using C6HSMGB was performed to obtain the final product. However, the reaction was not successful. Analyse the reaction by explaining what happened to the reaction and provide the correct synthetic method.

Consider the sequence of reactions below. In this sequence of reactions, an unsaturated ketone is treated with a Gilman reagent, followed by treatment with an aqueous base. The base allows a rapid equilibration to take place, producing the more stable stereoisomer of the product. 1. Et,CuLi 2. Equilibration with base For this process: show both stereoisomeric products, explain which is more stable, and explain why aqueous base allows equilibration between the stereoisomers.

Show how to carry out the transformation of benzene to phenol by going through a diazonium intermediate. At each step, either select the appropriate reagents or draw the correct product.

For the compound below, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.