The products of the following reaction CH_3-C | vedclass

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Question

(C) Ozonolysis of an internal alkyne followed by hydrolysis yields diketones as intermediate products,which are further oxidized to carboxylic acids.T

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$CH_3COOH + CH_3CH_2COOH$

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(C) Ozonolysis of an internal alkyne followed by hydrolysis yields diketones as intermediate products,which are further oxidized to carboxylic acids.The reaction proceeds as follows:$CH_3-C \equiv C-CH_2-CH_3$ $\xrightarrow{O_3} 	ext{ozonide intermediate}$ $\xrightarrow{H_2O} CH_3-CO-CO-CH_2-CH_3 + H_2O_2$The diketone $CH_3-CO-CO-CH_2-CH_3$ is then cleaved to form carboxylic acids:$CH_3-CO-CO-CH_2-CH_3 ightarrow CH_3COOH + CH_3CH_2COOH$Thus,the final products are acetic acid and propanoic acid.

The products of the following reaction $CH_3-C \equiv C-CH_2-CH_3 \xrightarrow[(2)\ H_2O]{(1)\ O_3}$ are:

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The ozonolysis $(O_3, H_2O)$ of $(CH_3)_2CH-C \equiv C-CH_3$ gives:

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