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NEET CHEMISTRYMedium

On ozonolysis, the alkene that gives the following product (structure missing) is:

A

Option 1 (Structure missing)

B

CH3CH2CH=CHCH2CH3\text{CH}_3\text{CH}_2\text{CH}=\text{CHCH}_2\text{CH}_3

C

CH3CH2CH=CHCH3\text{CH}_3\text{CH}_2\text{CH}=\text{CHCH}_3

D

Option 4 (Structure missing)

Step-by-Step Solution

Ozonolysis of alkenes involves the addition of an ozone molecule across the carbon-carbon double bond to form an ozonide, followed by its reductive cleavage (typically using zinc and water) to yield smaller carbonyl compounds (aldehydes or ketones) . By identifying the structures of the carbonyl products, the position of the double bond in the original alkene can be deduced.

Note: The specific chemical structure of the product was missing from the input data, so the exact starting alkene cannot be determined. Option 1 is marked correct based on the provided probable answer.

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