When trans-3-hexene is subjected to ozonolysis in the presence of an excess of acetaldehyde containing the isotope
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When trans-3-hexene is subjected to ozonolysis in the presence of an excess of acetaldehyde containing the isotope 18O, an ozonide is isolated that contains the isotope at one of the oxygens. Use the mechanism of ozonolysis to postulate a structure for the ozonide, including the position of the isotope.
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