What aspect of the structure of the alkene does ozonolysis not tell you?
Ozonolysis does not tell you about any stereochemistry there may have been in the original alkene.
Reductive ozonolysis converts an alkene into a pair of carbonyl compounds.
If the R groups are different, we can have cis/trans or E/Z stereochemistry.
If R₂ and R₄ are the groups with higher priority, 1 is a Z alkene. 2 is an E alkene.
But both give the same ozonolysis products.
You cannot distinguish between cis-but-2-ene and trans-but-2-ene by reductive ozonolysis.
They both give acetaldehyde as the only ozonolysis product.
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Ozonolysis of an alkene does not provide information about the stereochemistry of the resulting ozonide.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
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