Write a note on the preparation of carboxylic acid from alkyl benzene.

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(N/A) Aromatic carboxylic acids can be prepared by the vigorous oxidation of alkyl benzenes with chromic acid or acidic/alkaline potassium permanganate $(KMnO_4)$.
$(a)$ The entire side chain is oxidized to the carboxyl group $(-COOH)$ irrespective of the length of the side chain,provided that the benzylic carbon atom has at least one hydrogen atom.
$(b)$ Primary and secondary alkyl groups are oxidized to the carboxyl group in this manner.
$(c)$ If the benzylic carbon atom does not have any hydrogen atom (i.e.,tertiary alkyl group),then oxidation is not possible.
$(d)$ The reaction proceeds via the formation of a potassium salt (e.g.,potassium benzoate),which upon acidic hydrolysis $(H_3O^+)$ yields the corresponding aromatic carboxylic acid.
General reaction:
$C_6H_5-CH_2-R$ $\xrightarrow[\Delta]{KMnO_4, KOH} C_6H_5-COOK$ $\xrightarrow{H_3O^+} C_6H_5-COOH$

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$CH_3MgBr + CO_2$ $\xrightarrow{\text{Dry ether}} Y$ $\xrightarrow{H_3O^{\oplus}} Z$
Identify $Z$ from the following.

Consider the following reactions. From these reactions,which reaction will give carboxylic acid as a major product?
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Choose the correct answer from the options given below:

Which among the following compounds is $NOT$ used for the preparation of aromatic carboxylic acids from alkyl benzene?

The acid formed when propyl magnesium bromide is treated with carbon dioxide is:

The compound $X$ in the reaction is: $X$ $\xrightarrow{CH_3MgI} Y$ $\xrightarrow{\text{hydrolysis}} Mg(OH)I + CH_3COOH$

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