Draw the missing organic structures or select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed. Incorrect, 1 attempt remaining

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Q: NaCN acetonitrile

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Q: 5 Question: Synthesize the following compound from diethyl malonate or ethyl acetoacetate and any…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. Br2 (1 equiv) Drawing

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Q: Draw the product. Select Draw Rings More Erase H HgSO., H20 H2SO, -H-

A: This reaction give ketone compound instead of aldehyde because it is acid catalyzed hydrolysis…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. H2O pyridine Select to Draw

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Q: the major pr byproducts.

A: A question based on the reactions of alkenes with 1) Hg(OAc)2, H2O 2) NaBH4, NaOH. THis reaction is…

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A: It is an addition reaction in which hydration of unsaturated hydrocarbon alkene or alkyne…

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A: Hypochlorous acid (HOCl) acts as an oxidizing agent when reacting with primary alcohols.

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A: When a carbonyl compound is reacted with a Wittig Reagent (a triphenyl phosphonium ylide) it yields…

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A: Enone formation involves reaction of an enolate (formed from a carbonyl compound treated with a…

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Q: Draw a mechanism for the reduction of the carboxylic acid with lithium aluminum hydride (LAH).…

A: Lithium aluminum hydride is strong reducing agent. It reduces carboxylic acid to alcohol.

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A: The given reaction scheme is shown below.We have to add the curved arrow mechanism.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Incorrect, 1 attempt remaining…

A: LiAlH4 (Lithium aluminium hydride)is nucleophilic reagent. It reduces mostly all functional group.

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.