Suggest synthetic routes to each of the following form the indicated starting materials. You may use any other reagents. You can use other organic starting materials that is not explicitly excluded. However. all the carbons in the indicated starting materials have to end up in the final products. ### Transcription for Educational Use#### Chemical Reactions and Structures**f.** - Reaction: - Starting material: \[ \text{OPh} \text{from} \] - Product: \[ \text{OH} \] \[ + \text{HOPh} \]- Structure: - The reaction involves an unsaturated hydrocarbon chain ending with an OPh (phenoxy group) transforming into an alcohol (OH).**g.**- Reaction: - Starting material: \[ \text{from} \] - Product: Cyclohexanol- Structure: - Initial structure has a linear chain with hydroxyl groups (OH) that changes to a cyclic alcohol, cyclohexanol.### DescriptionThe diagram illustrates two chemical reactions where functional groups in the starting materials are modified to produce different compounds. Reaction f involves the conversion of a phenoxy group into an alcohol, indicating a nucleophilic substitution or similar transformation. In Reaction g, a linear diol transforms into a cyclic alcohol, suggesting a cyclization reaction.

f. The product can be synthesized as follows: 1. Hydrogenation with H2/Pd to reduce the double bond 2. Preparation of alkoxide on reaction with NaOH 3. Williamson Ether synthesis to form ether g. The product can be synthesized as follows: 1. Dehydration of alcohol with H2SO4 2. Reductive ozonolysis with O3/Me2S 3. Reduction of the aldehyde with NaBH4