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- Please complete the following question. There is no need to provide an explaination. 20Identify the best reagents to complete the following reaction. Options are included.Suggest a strategy to convert the alcohol into the iodide below. You may need multiple steps. 6) Suggest a strategy to convert the alcohol into the iodide below. You may need multiple steps. OH
- Complete each acid-base reaction and predict whether the position of equilibrium lies toward the left or toward the right. (a) CH3CCH+CH3CH2ONa+CH3CH3OH (b) CH3CCCH2CH2OH+Na+NH2NH3(l)Suggest how you would convert cyclohexanol (A) to B. HO "O-H A BProvide the reagent necessary to carry out the following conversation. You may need more than one step.
- Rank these compounds in order of decreasing acidity.Provide the reagents necessary to complete the following reactions. More than one step may be necessary, if so number separate steps.When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels,at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.
- When trichloroacetaldehyde is dissolved in water, almost all of it is converted to the hydrate. Chloral hydrate, the product of the reaction, is a sedative that can be lethal. A cocktail laced with it is known—in detective novels, at least—as a “Mickey Finn.” Explain why an aqueous solution of trichloroacetaldehyde is almost all hydrate.Show and explain reagents and expiramental conditions to synthesize each compound from 1- propanol.(b) Draw a stepwise mechanism for the following transformation from A to B. This reaction is one of the key steps in a synthesis of lysergic acid diethyl amide (aka LSD). CI A CH ₂ AIC13 B CH₂ several steps away from lysergic acid diethyl amide (LSD)
