answersLogoWhite

0

What else can I help you with?

Related Questions

What is the chemical structure of sunflower methyl ester and pongamia methyl ester?

it when .............. somting and somthing are put togather


Is methyl propionate an ester?

Yes, methyl propionate is an ester. It is formed by the condensation reaction between methanol and propionic acid, resulting in the formation of an ester linkage.


Is methyl benzoate an ester?

Methyl benzoate, an organic compound, is an ester. It is a colorless liquid that is not soluble in water and has a fruity smells. Some uses for methyl benzoate are as a solvent and a pesticide.


What is the common name for methyl propionate?

As far as I know, that is the common name.


What is the name of the Ester in bananas?

3- methyl butyl methanoate


What is the chemical structure of the smallest acyclic ester?

The smallest acyclic ester is methyl formate, with the chemical structure CH3OCHO.


What is the reaction between glycine methyl ester hydrochloride and acrylonitrile?

The amino group of glycine methyl ester hydrochloride reacts with the double bond of acrylonitrile, it occurs the Michael reaction, then generates CNCH2CH2NHCH2CO2Me.


Is Methylparaben an alcohol derivitive?

No, it is the methyl ester of p-hydroxybenzoic acid.


How does methyl stearate compare to methyl oleate?

Methyl stearate is a saturated fatty acid methyl ester, while methyl oleate is an unsaturated fatty acid methyl ester. Methyl oleate has a higher degree of unsaturation due to a double bond in its carbon chain, making it more flexible and less rigid than methyl stearate. Additionally, methyl oleate may have different physical properties, such as a lower melting point, compared to methyl stearate.


What is more polar methyl salicylate or salicylic acid?

salicylic acid (an acid) is more polar than methyl salicylate (an ester)


What is the difference between methyl stearate and hexadecanoic acid isopropyl ester?

One side methyl group- otherwise virtually identical identical- formula is the same. I bet the properties are very close. That methyl group in isopropyl hexadeconoate probably has a bit more effect on the oxyl main chain than if it was far away- probably slightly more acidic.


Formic acid plus 2-methyl propanol?

This reaction would likely result in the formation of an ester through a Fischer esterification reaction. The formic acid would react with 2-methyl propanol to form methyl 2-methyl propanoate (methyl isobutyrate) along with water as a byproduct. This ester has a fruity odor and is often used in the fragrance industry.