The functional group is ester with the general formula, RCOOR'
The functional group in a triglyceride is an ester group. It forms when a glycerol molecule reacts with three fatty acids through dehydration synthesis, resulting in the formation of three ester bonds.
Camptothecin contains a lactone functional group and a tertiary amine functional group in its structure.
The functional groups in phacetin are an ester group (-COO-), an amide group (-NH-), and an aromatic ring.
An ester group is probably the most easily hydrolyzed functional group. Especially at physiologic pH.
The ketone functional group is more acidic than the ester functional group. This is because the ketone group has a more stable conjugate base due to resonance stabilization, making it easier to lose a proton and therefore more acidic.
Hi Jer, if you are reading this, Ester is one of the functional group
ester
The functional group in ethyl butyrate is the ester functional group, which consists of a carbonyl group bonded to an oxygen atom, C=O-O-R. In ethyl butyrate, the R group is an ethyl group.
There are two functional groups: 1. Carboxyl group 2. Ester group
In ethyl acetate, you would find an ester functional group, which consists of a carbonyl group bonded to an oxygen atom and an alkyl group.
The functional group found in polyester is an ester group, which is formed by the reaction between an alcohol group and a carboxylic acid group. This ester group is what gives polyester its characteristic properties such as durability and resistance to wrinkles.
The functional group in a triglyceride is an ester group. It forms when a glycerol molecule reacts with three fatty acids through dehydration synthesis, resulting in the formation of three ester bonds.
Camptothecin contains a lactone functional group and a tertiary amine functional group in its structure.
Ester Alcohol Ether Amine
The functional groups in phacetin are an ester group (-COO-), an amide group (-NH-), and an aromatic ring.
An ester group is probably the most easily hydrolyzed functional group. Especially at physiologic pH.
The ketone functional group is more acidic than the ester functional group. This is because the ketone group has a more stable conjugate base due to resonance stabilization, making it easier to lose a proton and therefore more acidic.