2 chlorobutane to acetic acid
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Explanation:
CO2 takes the place of the MgCl at the 2 position of butane, and once you add a proton source (H3O+) it becomes a carboxylic acid. The carbon of the newly added COOH becomes part of the backbone of the molecule and using the proper nomenclature rules, now you have 2-methylbutanoic acid.
Answered by
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CO2 takes the place of the MgCl at the 2 position of butane, and once you add a proton source (H3O+) it becomes a carboxylic acid. The carbon of the newly added COOH becomes part of the backbone of the molecule and using the proper nomenclature rules, now you have 2-methylbutanoic acid.
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