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 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]- CH3-COO- Na+ + H2O + CO2
It can be prepared by reacting a potassium-containing base such as potassium hydroxide or potassium carbonate with acetic acid: 2CH3COOH + K2CO3 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.
Propane-1,2,3-tricarboxylic acid, also known as tricarballylic acid, carballylic acid, and beta-carboxyglutaric acid, is a tricarboxylic acid that has three carboxylic acid functional groups.
Amyl acetate (also pentyl ethanoate, pentyl acetate) is an organic compound and an ester with the chemical formula CH3COO(CH2)4CH3 and the molecular weight 130.18 g/mol. It has a scent similar to bananas[1] and apples which is not detectable by all people.
Amyl acetate (also pentyl ethanoate, pentyl acetate) is an organic compound and an ester with the chemical formula CH3COO(CH2)4CH3 and the molecular weight 130.18 g/mol. It has a scent similar to bananas[1] and apples which is not detectable by all people.
Aluminium acetates are the aluminium salts of acetic acid.
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