By the reaction with NaOH and excess Cl2
Tri- Chloro- Ethylene
Malonic acid has pKa values of 2.83 (pK1) and 5.69 (pK2). If malonic esters are used then on treatment with a strong base like sodium ethoxide, the methylene (-CH2-) hydrogen can be deprotonated, but I am not sure if that is possible for malonic acid as that will lead to a tri-anion.
No, it is a tri-nary compound.
Tri-sodium citrate is the triple basic anion of citric acid. So without protons it is basic.
There are several organic acids without COOH group , example is carbolic acid , a phenol, picric acid which is 2,4,6 tri-nitro phenol, barbituric acid, ascorbic acid etc
by urea hydrogen peroxide reaction with tri fluro acetic anhydride
Tri- Chloro- Ethylene
1-1-1 Tri-Chloro-Ethane
Malonic acid has pKa values of 2.83 (pK1) and 5.69 (pK2). If malonic esters are used then on treatment with a strong base like sodium ethoxide, the methylene (-CH2-) hydrogen can be deprotonated, but I am not sure if that is possible for malonic acid as that will lead to a tri-anion.
Glycogen is extracted from animal tissue. This tissue is actually pretty tough and to liberate the glycogen from it, the tissue has to be ruptured, broken down nicely, so that all the glycogen is available for extraction. This grinding (homgenizing) process is aided by the presence of sand and TCA (Tri-Chloro Acetic acid). TCA is a higly corrosive agent and helps in rupturing the tissue.
this is the combination of tri chloro fluro ethane and isopropyl alcohol
give me the example of tri
No, it is a tri-nary compound.
a tria basic acid is a acid containing three replacable hdrogen atoms
Tri-sodium citrate is the triple basic anion of citric acid. So without protons it is basic.
Because it goes around and around as in a unicycle wheel.
The real answer compared to all of those other questions is oxaloacetic acid.