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The acetate anion, [C2H3O2]-, is a carboxylate and is the conjugate base of acetic acid. The acetate ion is formed by the deprotonation of acetic acid:
CH3COOH ? CH3COO- + H+

- Sodium Acetate
- Potassium Acetate


Sodium Acetate
Sodium acetate is inexpensive, and is usually purchased from chemical suppliers, instead of being synthesized in the laboratory. It is sometimes produced in a laboratory experiment by the reaction of acetic acid with sodium carbonate, sodium bicarbonate, or sodium hydroxide to name a few bases which contain sodium.

CH3-COOH + Na+[HCO3]- potassium fluoride, potassium fluoborate, tin fluoborate, copper fluoborate, potassium bi fluoride, ammonium silico fluoride, potassium silico fluoride CH3-COO- Na+ + H2O + CO2






Potassium Acetate
It can be prepared by reacting a potassium-containing base such as potassium hydroxide or potassium carbonate with acetic acid: 2CH3COOH + K2CO3 potassium fluoride, potassium fluoborate, tin fluoborate, copper fluoborate, potassium bi fluoride, ammonium silico fluoride, potassium silico fluoride 2CH3COOK + CO2 + H2O This sort of reaction is known as an acid-base neutralization reaction. Potassium acetate is the salt that forms along with water as acetic acid and potassium hydroxide are neutralized together.

Conditions/substances to avoid are: moisture, heat, flames, ignition sources, and strong oxidizing agents.







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