The following reaction is given:xrightarrow{t | vedclass

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(B) The reaction is an example of Kolbe's electrolysis of a dicarboxylic acid salt.$1$. Upon electrolysis,the carboxylate ions $(R-COO^-)$ lose electr

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(B) The reaction is an example of Kolbe's electrolysis of a dicarboxylic acid salt.$1$. Upon electrolysis,the carboxylate ions $(R-COO^-)$ lose electrons at the anode to form carboxyl radicals $(R-COO^{\bullet})$.$2$. These radicals undergo decarboxylation to release $CO_2$ and form alkyl radicals $(R^{\bullet})$.$3$. In this specific case,the two radical centers formed on the cyclohexane ring combine to form a double bond,resulting in the formation of naphthalene,which is stable due to its aromatic character.Therefore,the product $A$ is naphthalene.

The following reaction is given:
$\xrightarrow{\text{Electrolysis}} A$
$A$ is

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The following reaction is given:$\xrightarrow{\text{Electrolysis}} A$$A$ is