Which of the following reactions will not pro | vedclass

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(A) Let's analyze each reaction:$(A)$ $CH_3-CH_2-SO_3H + NaHCO_3 \rightarrow CH_3-CH_2-SO_3Na + H_2O + CO_2$. Sulfonic acids are stronger than carboni

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$CH_3-CH_2-SO_3H \xrightarrow{NaHCO_3}$

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(A) Let's analyze each reaction:$(A)$ $CH_3-CH_2-SO_3H + NaHCO_3 \rightarrow CH_3-CH_2-SO_3Na + H_2O + CO_2$. Sulfonic acids are stronger than carbonic acid,so they react with $NaHCO_3$ to release $CO_2$.$(B)$ Malonic acid $(HOOC-CH_2-COOH)$ on heating undergoes decarboxylation to produce acetic acid and $CO_2$.$(C)$ Kolbe's electrolysis of sodium propionate $(CH_3-CH_2-COONa)$ produces $CO_2$ at the anode along with butane and $H_2$.$(D)$ $\beta$-keto acids (like the one shown in the image) undergo decarboxylation on heating to release $CO_2$.Wait,re-evaluating $(A)$: While sulfonic acids are strong,the reaction $R-SO_3H + NaHCO_3 \rightarrow R-SO_3Na + H_2O + CO_2$ is standard. However,in many contexts,this question is designed to test the acidity relative to $NaHCO_3$. All options listed actually produce $CO_2$. Let's re-examine the options provided. If the question implies which one does $NOT$,and all do,there might be a nuance. Actually,all these reactions are known to produce $CO_2$. Given the standard nature of these reactions,all produce $CO_2$.

Which of the following reactions will not produce $CO_2$?

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