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Potassium permanganate is an inorganic compound with the chemical formula KMnO 4. ... For the standardization of KMnO 4 solutions, reduction by oxalic acid is often ...
It is the sodium salt of oxalic acid. It contains sodium cations Na + and oxalate anions C 2 O 2− 4. It is a white, crystalline, odorless solid, that decomposes above 290 °C. [2] Sodium oxalate can act as a reducing agent, and it may be used as a primary standard for standardizing potassium permanganate (KMnO 4) solutions.
Oxalic acid's main applications include cleaning or bleaching, especially for the removal of rust (iron complexing agent). Its utility in rust removal agents is due to its forming a stable, water-soluble salt with ferric iron, ferrioxalate ion. Oxalic acid is an ingredient in some tooth whitening products.
Potassium permanganate will decompose into potassium manganate, manganese dioxide and oxygen gas: 2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2 This reaction is a laboratory method to prepare oxygen, but produces samples of potassium manganate contaminated with MnO 2 .
A permanganate can oxidize an amine to a nitro compound, [7] [8] a secondary alcohol to a ketone, [9] a primary alcohol or aldehyde to a carboxylic acid, [10] [11] a terminal alkene to a carboxylic acid, [12] oxalic acid to carbon dioxide, [13] and an alkene to a diol. [14] This list is not exhaustive. In alkene oxidations one intermediate is a ...
Potassium hydrogenoxalate is a salt with formula KHC 2 O 4 or K + ·HO 2 C-CO 2 −.It is one of the most common salts of the hydrogenoxalate anion, and can be obtained by reacting potassium hydroxide with oxalic acid in 1:1 mole ratio.
Depending on the conditions in which the titration is performed, the manganese is reduced from an oxidation of +7 to +2, +4, or +6. In most cases, permanganometry is performed in a very acidic solution in which the following electrochemical reaction occurs: [3]
Warm concentrated potassium permanganate (KMnO 4) will react with an alkene to form a glycol. Following this dihydroxylation , the KMnO 4 can then cleave the glycol to give aldehydes or ketones. The aldehydes will react further with (KMnO 4 ), being oxidized to become carboxylic acids .