The following synthesis will not work and will not provide the desired product. Show how you would fix it by modifying the current synthesis to one that will provide the desired product. OH H' EIMgBr H2 NaOH, H20 THF then H* MeO Pd/C, E1OH MeO

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A: This can be done by using a base to form a nucleophile which can then attack an epoxide ring.

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A: Applying concept of organic synthesis and reagent.

Q: 2 без OH НО 3 4 5 OH

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Q: OH H.

A: In the given transformation, carboxylic acid(-COOH) is converted to an      aldehyde(-CHO)

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Q: Diazomethane can be used to convert a carboxylic acid to a methyl ester. Propose a mechanism for…

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Q: Br EtO ELOH Br HS THE он SOCI, pyridine

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Q: Predict the product of the following reaction. 200 None of these NaOH HO HO 00 00 00 00 HO B HO- HO…

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