Which of the following compounds on ozonolysi | vedclass

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(C) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds (aldehydes or ketones). Aldehydes give a positiv

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but$-2-$ene

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(C) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds (aldehydes or ketones). Aldehydes give a positive silver mirror test with Tollen's reagent,whereas ketones do not. For an aldehyde to be formed,at least one hydrogen atom must be attached to the carbon atoms of the $C=C$ double bond. Let's analyze the options: $(A)$ $1,2$-dimethylcyclohexene: Ozonolysis yields a diketone (hexane$-2,5-$dione),which does not react with Tollen's reagent. $(B)$ $2,3$-dimethylbut$-2-$ene: Ozonolysis yields two molecules of acetone (propanone),which is a ketone and does not react with Tollen's reagent. $(C)$ $but-2-ene$: Ozonolysis yields two molecules of acetaldehyde $(CH_3CHO)$,which is an aldehyde and gives a positive silver mirror test with Tollen's reagent. $(D)$ $isopropylidenecyclohexane$: Ozonolysis yields cyclohexanone and acetone,both of which are ketones and do not react with Tollen's reagent. Therefore,the correct option is $C$.

Which of the following compounds on ozonolysis gives a product that gives a silver mirror with Tollen's reagent?

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