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- Devise a synthesis of each compound from benzene. You may usealcohols with one or two carbons and any inorganic reagents.Devise a synthesis of each compound from benzene, any organic alcohols having four or fewer carbons, and any required reagents.Synthesize each compound from cyclohexanol, ethanol, and any other needed reagents.
- Devise concise syntheses for the following transformations. Clearly show the reagent andproduct for each step. All syntheses can be accomplished in two steps.Identify the best reagents to complete the following reaction. H,11. Devise a synthesis of each compound from benzene, any organic alcohols having four or fewer carbons, and any required reagents.
- Synthesize the following compound from cyclohexanone and any other organic and inorganic reagents you need.Devise a synthesis of each compound from benzene. You may also useany organic compounds having four or fewer carbons and any requiredinorganic reagents.Devise a synthesis of each compound from cyclohexene and any required organic compounds or inorganic reagents.
- Devise a synthesis of attached compound from CH3CH2OH as the only organic starting material; that is, every carbon in the product must come from a molecule of ethanol. You may use any other needed in organic reagents.Devise a synthesis of each compound from benzene and organic alcohols containing four or fewer carbons. You may also use any required organic or inorganic reagents.Devise a synthesis of each compound from CH3CH2CH2CO2Et, benzene, and alcohols having ≤ 2 C's. You may also use any required organic or inorganic reagents.