How do cis and trans isomers arise in cinnamaldehyde?
Well, you have an disubstituted olefin..........
.........which can generate cis and trans isomers given the disposition of the substituents about the olefinic bond:
Cinnamon oils from natural sources contain the trans isomer as shown.
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Cis and trans isomers in cinnamaldehyde arise due to the different spatial arrangements of the double bond between the carbon atoms in the side chain.
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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.
- Why can geometric isomers occur?
- Which is a more stable conjugated compound: the cis form or the trans form and why?
- What molecules can have cis and trans isomers?
- Does the energy barrier cause the existence of two distinct isomers?
- When is the cis-trans system not effective for naming geometric isomers?

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