The products of the reaction CH_3 - C equiv C | vedclass

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(C) Ozonolysis of an internal alkyne followed by hydrolysis results in the cleavage of the triple bond to form two carboxylic acid molecules.For the g

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$CH_3COOH + CH_3CH_2COOH$

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(C) Ozonolysis of an internal alkyne followed by hydrolysis results in the cleavage of the triple bond to form two carboxylic acid molecules.For the given alkyne $CH_3 - C \equiv C - CH_2CH_3$ (pent$-2-$yne):Step $1$: The triple bond is cleaved.Step $2$: The carbon atoms of the triple bond are oxidized to carboxylic acid groups.$CH_3 - C \equiv C - CH_2CH_3 \rightarrow CH_3COOH + CH_3CH_2COOH$.Thus,the products are acetic acid $(CH_3COOH)$ and propanoic acid $(CH_3CH_2COOH)$.

The products of the reaction $CH_3 - C \equiv C - CH_2CH_3 \xrightarrow[(ii) \text{ Hydrolysis}]{(i) O_3}$ are .....

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