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cinnamaldehyde is a aldehyde hence cinnam(aldehyde)

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12y ago
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1mo ago

Cinnamaldehyde is an aldehyde. Its structure contains an aldehyde functional group (-CHO) attached to a benzene ring.

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10y ago

it is an unsaturated aldehyde.

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Q: Is cinnamaldehyde an aldehyde or ketone?
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Related questions

What aldehyde or ketone present in candies with cinnamon flavor?

Cinnamaldehyde is the primary compound responsible for the cinnamon flavor in candies.


What is the name of the molecular structure of cinnamaldehyde?

The molecular structure of cinnamaldehyde is a benzene ring with an aldehyde group (CHO) and an unsaturated carbon chain.


Is benzaldehyde ketone or aldehyde?

An aldehyde (as the name says)


What is the chemical name of oil of cinnamon?

The chemical name of oil of cinnamon is cinnamaldehyde.


What is aldehyde and ketone?

They have the same functional group.


Is Benzyl Acetate a Aldehyde or Ketone?

Benzyl acetate is neither an aldehyde nor a ketone. It is an ester, specifically the ester of benzyl alcohol and acetic acid.


Is vanillin an aldehyde or a ketone?

From its structure, we can see that vanillin does not have a ketone functional group, but it has an aldehyde. It also has a phenol and ether functional group. For that reason, I wouldn't categorize is as just an aldehyde.


What functional groups are present in the molecule responsible for the flavor of cinnamon?

The molecule responsible for the flavor of cinnamon is cinnamaldehyde. It contains an aldehyde functional group, which is responsible for its strong aromatic and spicy flavor.


What is an aldolization?

An aldonization is the formation of an aldol - an aldehyde or ketone with a hydroxy group in the beta- position - usually from a correpsonding aldehyde.


Is butanedione an aldehyde or ketone?

Since it is "dione", it is a ketone, and there should be a comma between the 2 and 3 such as in 2,3-butanedione.


Is diacetyl an aldehyde or a ketone?

Diacetyl is a ketone. It has a structure with two carbonyl groups attached to a central carbon atom.


In cross aldol condensation between aldehyde and ketone why aldehyde is always an electrophile?

In a cross aldol condensation between an aldehyde and a ketone, the aldehyde is always the electrophile because it has a reactive carbonyl carbon that is more electrophilic compared to the carbonyl carbon of the ketone. This is due to the presence of the less electron-donating substituent (hydrogen) attached to the carbonyl carbon of the aldehyde.