In reductive ozonolysis, the double bond in the hydrocarbon is cleaved, and oxygen atoms are inserted to form carbonyl compounds. The hydrocarbon provided yields ethanol (\( \text{CH}_3\text{CH}_2\text{OH} \)) and propanone (\( \text{CH}_3\text{COCH}_3 \)). To determine the original hydrocarbon:
Draw the products and combine them by removing oxygen atoms.
Reconnect the resulting fragments to form the hydrocarbon.
The original hydrocarbon is identified as \( \text{2-Methylprop-1-ene} \), which cleaves to give the specified products.
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Final Answer:
\[
\boxed{\text{2-Methylprop-1-ene}}
\]