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write a detailed arrow pushing mechanism for the synthesis of n- Hexyl acetate reaction?
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- write the product in the following reaction?1) Nitriles are typically hydrolyzed to form what class of compounds? 2) what must one keep in mind when performing the hydrolysis of a nitrile to a carboxylic acid? 3) why are nitriles over-looked as carboxylic acid derivatives?Draw the intermediate product and the final product for the synthesis of ethyl 3-coumarin carboxylate.
- Kindly provide an explanation thank youExplain why methyl trifluoroacetate, CF3CO2CH3, is more reactive than methyl acetate, CH3CO2CH3, in nucleophilic acyl substitution reactions.On synthesis of esters via nucleophilic acyl substitution: Write the chemical equation involved in the reaction between the excess acid and NaHCO3. Given this, briefly explain why NaHCO3 is preferred over NaOH for the neutralization of excess acid. Also, explain how excess alcohol was eliminated from the crude product.
- What is the role of the acetic acid in the oxidation of Cyclohexanol to Cyclohexanone? Write the balanced chemical reaction between acetic acid and sodium hypochlorite.Explain the general procedure for the laboratory preparation of the synthesis of Aniline from benzoic acid. (paragraph form) Explain the chemistry behind the synthesis of Aniline from benzoic acid. (paragraph form)Explain the experimental procedure of the laboratory preparation of the synthesis of Aniline from benzoic acid. (paragraph form) Explain the chemistry behind the synthesis of Aniline from benzoic acid. (paragraph form)