Draw the structure of the ethyl acetate and name using the IUPAC system. Compare your 1H NMR with the NMR provided for the pure ester, what conclusions can be drawn from this comparison?
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- A fellow lab student is attempting to identify his unknown organic compound by using the Tollens' test. He adds Tollens' reagent to a sample of benzaldehyde and to his unknown. You notice that neither his benzaldehyde or unknown sámple solution formed a silver precipitate. The student confidently proclaims that his unknown must not be an aldehyde. Is he correct? Yes, because his unknown solution failed to form a silver precipitate that indicates the presence of an aldehyde. O Yes, because the Tollens' test only forms a silver precipitate in the presence of an aromatic aldehyde. O No, because his positive control did not form a silver precipitate, therefore he should gently heat the samples to verify the result. No, because the Tollens' test only forms a silver precipitate in the presence of a methyl ketone.Draw a flow-chart for the separation of benzoic acid and ethyl benzoate . Which compound can be found in which step, in which form and where?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.complete the reaction by adding reagents or prodcts Please provide only typed answer solution no handwritten solution needed allowed3. You are given a mixture of aspirin, phenol, and naphthalene that you need to separate. i) Draw the structures of each, and identify if they are acidic, basic, or neutral compounds. For each compound draw their reaction with the appropriate acidic or basic conditions that will change their solubility and allow them to be separated. ii) What modifications would you have to make to the experimental protocol in order to separate these three compounds? Provide specifics.
- explain in detail how you would separate benozic acid from phenol, using either lithium hydroxide, sodium bicarbonate, and any acid?Two reactions occur when sodium hydroxide is added to methyl salicylate. One is immediate and one only occurs with reflux over time. What type of reaction occurs immediately and with which functional group on methyl salicylate does it react? What type of reaction occurs with reflux over time and with which functional group on methyl salicylate does it react?Iodoform Test to identify methyl ketones; Write whether the following ketones are positive or negative for the Iodoform Test. Methyl Ethyl ketone (Unknown) Acetophenone