Draw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in a Grignard synthesis of the alcohol shown. OH
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- Draw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in a Grignard synthesis of the alcohol shown.Include a paragraph to describe the procedure (synthesis of dibenzalacetone) Make sure to discuss the role of the reactants below in the experiment. Sodium hydroxide Ethyl alcohol Acetone BenzaldehydeDraw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in a Grignard synthesis of the alcohol shown. You do not have to consider stereochemistry. If there is more than one combination, draw only one. Draw one structure per sketcher.
- Draw structural formulas for the major organic product of the reagents shown11. Starting with 1,3-propanediol, ethanol, and 1-propanol, design a synthesis for 2-ethylpentanoic acid. Use any other reagents that are needed.Compounds A, B, and C which are all alcohols are subjected to the Lucas test. An oily layer was formed almost instantly after the addition of reagents to Compound C. For compound A, it took several minutes before an oily layer was formed. Meanwhile, it took at least one hour with compound B before an oily layer was observed. What could be compound B? Choices: Ethanol Isopropyl alcohol tert-butyl alcohol
- Draw a structural formula for the product formed by treating reactants with sodium ethoxide in ethanol under conditions of the Michael reaction.Draw a structural formula for the product of the reaction shownExplain why the acid-catalyzed dehydration of an alcohol is a reversible reaction, whereas the base-promoted dehydrohalogenation of an alkyl halide is an irreversible reaction.
- Draw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in a Grignard synthesis of the alcohol shown. Please draw a clear and detailed image.Esterification reactions, such as the one below, is a poor synthetic strategy as it leads to poor yields of the ester. What alternative could be done to produce more p-methylphenyl acetate? Replace the aromatic alcohol with a phenolate. Replace acetic acid with acetate. Replace the p-methylphenol with p-chlorotoluene. Replace acetic acid with acetyl chloride.Give the reagent for these reactions!