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Structure Of TFA Formula
The elements carbon, fluorine, oxygen, and hydrogen make up the TFA Formula. A nonmetallic element found in group 14 of the periodic table is carbon. It has an atomic number of six, and the letter C is used to denote it. Fluorine is a diatomic gas that has a pale yellow appearance and is extremely toxic. It is the most electronegative element in the periodic table’s group 17. It has an atomic number of nine, and the letter F is used to denote it. The nonmetal oxygen is a highly reactive nonmetal that belongs to the chalcogen group-16.It has an atomic number of 8, and the letter O is used to denote it. The most flammable, colourless, odourless, tasteless, and lightest gas is hydrogen. It has an atomic number of 1, and the letter H is used to denote it.
Preparation of Trifluoroacetic acid
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Properties Of TFA Formula
- TFA Formula has a molecular weight of 114.023 g/mol.
- TFA Formula has a density of 1.489 gmL-1.
Physical Properties of Trifluoroacetic acid
- Trifluoroacetic acid has a melting point of -15.4 °C.
- Trifluoroacetic acid has a boiling point of 72.4°C.
- TFA Formula has a 33 kJ/mol enthalpy of vaporisation.
- Trifluoroacetic acid appears as a colourless liquid.
- Trifluoroacetic acid has an unpleasant smell.
Chemical Properties of Trifluoroacetic acid
- The skin and eyes are corrosive to trifluoroacetic acid.
- The acidity of trifluoroacetic acid is greater than that of acetic acid because it contains three fluorine atoms.
- TFA Formula is water soluble.
- Fluorine atoms have a high level of negative inductive effects and are highly electron-withdrawing groups. As a result, carbon has a severe lack of electrons and is susceptible to losing the hydrogen atom in the main functional group.
Uses of Trifluoroacetic acid
TFA Formula is the abbreviation for trifluoroacetic acid. Trifluoroacetic acid has the chemical formula CF3CO2H. Acetyl chloride (CH3COCl) is treated in electrochemical fluorination to produce trifluoroacetic acid (TFA Formula). In acid-catalyzed reactions, the TFA Formula is employed, particularly when an ester is cleaved during the synthesis of peptides. Trifluoroethanoic acid is yet another name for it. Trifluoroacetate’s conjugate acid is TFA Formula. TFA Formula is denser than water and soluble in it. 2,2,2-Trifluoroacetic Acid is the IUPAC name for trifluoroacetic acid.
Trifluoroacetic acid has a strong smell and is a colourless, fuming liquid.
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