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Carboxylic acids are weak acids that reduce basic by releasing hydrogen ion salts. The carboxyl group of either a carbocation is bonded to either a phenyl ring to produce a methyl group with carbonyl group. An methyl or benzyl component may engage to the carboxyl member.

When strong acids combine with strong acids including $NaOH$ and $KOH$ to create carboxy compounds, these become entirely negated. By exchanging the ic acid (at the end) and ended up eating, the acetate cation is termed.

Sodium methanoate, sometimes sodium chloride formic acid, is really the sulfonate salt created while ammonia burns using $NaOH$.

Sodium $3$-chloropropanoate is really the sulfonate created when $3$-chloropropanoic acid mixes to $NaOH$.

Sodium benzoate seems to be the carboxylate salt created whenever benzoic acid mixes to $NaOH$.