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![6) Suggest a strategy to convert the alcohol into the iodide below. You may need multiple steps.
OH
A
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- 6) Suggest a strategy to convert the alcohol into the iodide below. You may need multiple steps. OH A ANYPlease complete the following question. There is no need to provide an explaination. 20Suggest 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)Provide the reagent necessary to carry out the following conversation. You may need more than one step.Suggest how you would convert cyclohexanol (A) to B. HO "O-H A B
- 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.1. Provide stepwise synthesis including reagents and intermediates for the following syntheses. OH COOH
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