Unbranched alkenes on ozonolysis give :- | vedclass

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(B) Ozonolysis of an unbranched alkene involves the cleavage of the $C=C$ double bond.For an unbranched alkene of the general form $R_1-CH=CH-R_2$,the

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Only aldehydes

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(B) Ozonolysis of an unbranched alkene involves the cleavage of the $C=C$ double bond.For an unbranched alkene of the general form $R_1-CH=CH-R_2$,the reaction with $O_3$ followed by reductive workup $(Zn/H_2O)$ results in the formation of two aldehyde molecules.The general reaction is: $R_1-CH=CH-R_2 \xrightarrow{O_3, Zn/H_2O} R_1-CHO + R_2-CHO$.Since the carbon atoms involved in the double bond are bonded to at least one hydrogen atom,the products are aldehydes.

Unbranched alkenes on ozonolysis give $:-$

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