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OH 1-Butyne Acetaldehyde Alkyne anions react with the carbonyl groups of aldehydes and ketones to form alkyayl alcohols. The reaction mechanism between 1-butyne and acetaldehyde includes the following steps: 1. Sodium amide deprotonates the terminal alkyne 2. The alkyne anion acts as a nucleophile and adds to the aldehyde carbonyl: 3. Proton transfer from solvent forms the product alcohol. Diagram the mechanism on a separate sheet of paper, and then draw the structure of the product(s) of step 2. . You do not have to consider stereochemistry . You do not have to explicitly draw H atoms. Draw organic species only . Do not include counter-jous, e.g. Na . I, in your answer

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Salution laN Mechanism Step erd 내 NaN

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