How do cis and trans isomers arise in cinnamaldehyde?

Answer 1

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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Answer 2

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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Answer from HIX Tutor

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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