Q.Propanal and pentan-3-one are the ozonolysis products of an alkene? What is the structural formula of the alkene?
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Start your 14-day free trial to unlock the full solution →The alkene must have a carbon‑carbon double bond that, when cleaved by ozone, gives exactly propanal () and pentan‑3‑one (). Reconnecting the two carbonyl fragments across the original double bond yields 3‑ethylhex‑3‑ene.
Why this approach works
Ozonolysis is a clean chemical “scissors” that cuts a bond and replaces each carbon of the double bond with a carbonyl group ().
- If the carbon had two hydrogens attached, you get an aldehyde ().
- If it had one hydrogen and one alkyl group, you still get an aldehyde.
- If it had two alkyl groups (no hydrogen), you get a ketone ( with two groups).
So the two products tell us exactly what was attached to each end of the original double bond. To find the alkene, we simply “glue” the two carbonyl fragments back together — removing the oxygen atoms and joining the two carbons with a double bond.
Step‑by‑step reconstruction
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Identify the carbonyl fragments
- Propanal: The aldehyde carbon (the ) came from a carbon that had one hydrogen and one alkyl group () attached to the original double bond.
- Pentan‑3‑one: The ketone carbon (the ) came from a carbon that had two alkyl groups ( and ) attached to the original double bond — no hydrogen.
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Reconnect the two carbons
Remove the oxygen from each carbonyl and join the two carbons with a double bond.
- Left fragment (from propanal):
- Right fragment (from pentan‑3‑one):
Putting them together:
- Name the alkene The longest chain containing the double bond has 6 carbons: Number from the end nearer the double bond: …
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