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  • Formaldehyde can be used to preserve dead animals.
  • Acetone is a common fingernail polish remover and is a solvent. Acetone is very flammable.
  • 2-Butanone (MEK, methyl ethyl ketone) is used as a solvent and paint stripper. 2-Butanone is very flammable.
  • Benzaldehyde is an almond extract.
  • (-)-Carvone is used as spearmint flavoring.
  • (+)-Carvone is used as caraway seed flavoring. Vanillin is the vanilla flavoring.
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How will you characterize the rate of reaction of an aldehyde compared to an aliphatic aldehyde?

Typically aromatic groups attached to functional groups increase the reaction over that of an aliphatic groups. Aromatic aldehydes (e.g. benzaldehyde, C6H5.CHO), are also known which undergo a number of chemical reaction which do nor occur for aliphatic aldehydes and which are unique to aromatic aldehydes.


Which aldehyde do not give fhelings test?

Aromatic aldehydes, such as benzaldehyde, typically do not give a positive Fehling's test due to the lack of alpha-hydrogens required for oxidation. Aromatic aldehydes are not easily oxidized in the Fehling's test compared to aliphatic aldehydes.


What are the formulas of aldehydes and ketones?

The general formula for aldehydes is RCHO (where R is a hydrocarbon group), and the general formula for ketones is R2CO (where R is a hydrocarbon group).


What is the colour of semicarbazone of aldehydes?

The semicarbazone derivatives of aldehydes typically appear as yellow to orange crystalline solids. The exact color can vary depending on the specific aldehyde used and its substituents. These compounds are often characterized by their formation through the reaction of aldehydes with semicarbazide in the presence of an acid catalyst.


The plasmid pARA-R has been genetically modified for what purpose?

The plasmid pARA-R has been genetically modified to contain aarF gene from the Candida boidinii yeast which codes for aryl-alcohol dehydrogenase, an enzyme that can convert aromatic alcohols to their corresponding aldehydes. This modification allows for the efficient conversion of aromatic alcohols to aldehydes in biotransformation processes.

Related Questions

Difference between aromatic and aliphatic aldehyde?

Aromatic aldehydes contain an aromatic ring in their structure, while aliphatic aldehydes have a straight or branched carbon chain. Aromatic aldehydes typically have a stronger smell compared to aliphatic aldehydes due to their benzene ring. Aromatic aldehydes are commonly found in natural sources like plants, while aliphatic aldehydes are more often associated with industrial processes.


What is the difference in acidity between aldehydes and ketones?

Aldehydes are generally more acidic than ketones due to the presence of a hydrogen atom attached to the carbonyl group in aldehydes, which can be easily donated as a proton. This makes aldehydes more reactive towards nucleophiles compared to ketones.


Which two groups have the same functional group?

ketones and aldehydes


How will you characterize the rate of reaction of an aldehyde compared to an aliphatic aldehyde?

Typically aromatic groups attached to functional groups increase the reaction over that of an aliphatic groups. Aromatic aldehydes (e.g. benzaldehyde, C6H5.CHO), are also known which undergo a number of chemical reaction which do nor occur for aliphatic aldehydes and which are unique to aromatic aldehydes.


What homologus series is ethanal in?

Aldehydes


Which aldehyde do not give fhelings test?

Aromatic aldehydes, such as benzaldehyde, typically do not give a positive Fehling's test due to the lack of alpha-hydrogens required for oxidation. Aromatic aldehydes are not easily oxidized in the Fehling's test compared to aliphatic aldehydes.


Polyhydroxy derivatives of aldehydes or ketoens are?

Carbohydrates


What are the formulas of aldehydes and ketones?

The general formula for aldehydes is RCHO (where R is a hydrocarbon group), and the general formula for ketones is R2CO (where R is a hydrocarbon group).


Why are aldehydes more reactive than ketones towards nucleophile?

Aldehydes are less sterically hindered than ketones. Also, aldehydes have fewer electron donating groups (EDG's) which can stabilize an electron-poor area. The extra carbon chain that ketones have that aldehydes do not have are the reason for both of these things. The neighboring carbon to the carbonyl carbon is an EDG and the carbon chain causes steric hindrance.


What has the author Lynne Herman Ulich written?

Lynne Herman Ulich has written: 'The reactions between acid halides and aldehydes' -- subject(s): Aldehydes, Halides


What is aldehydes in PAS stain?

Aldehydes are what create the color in any stain; especially the PAS stain. In reference, the aldehyde are the pigments that can cause permanent staining in a fabric.


What is the colour of semicarbazone of aldehydes?

The semicarbazone derivatives of aldehydes typically appear as yellow to orange crystalline solids. The exact color can vary depending on the specific aldehyde used and its substituents. These compounds are often characterized by their formation through the reaction of aldehydes with semicarbazide in the presence of an acid catalyst.