If potassium permanganate is oxidized under alkaline conditions, it can open double bonds to form manganate intermediates, and then manganate intermediate body becomes manganese dioxide precipitation, and double bonds are oxidized to neighboring glycol. If it is acidic,Oxidation under conditions, the carbon skeleton is completely disconnected, and the ketone or carboxylic acid is generated.
If potassium permanganate is oxidized under alkaline conditions, it can open double bonds to form manganate intermediates, and then manganate intermediate body becomes manganese dioxide precipitation, and double bonds are oxidized to neighboring glycol. If it is acidic,Oxidation under conditions, the carbon skeleton is completely disconnected, and the ketone or carboxylic acid is generated.
Potassium permanganate is oxidized, while oleic acid contains C \u003d C, which can be used as a reducing agent, just like the potassium permanganate reacts with ethylene, oleic acid is oxidized into a smaller molecular weight acid, and controlling potassium permanganateIt is restored to manganese dioxide (as long as the solution is neutral, it can be achieved); oleic acid is also a dispersant. 8KMNO4 + 3R-CH \u003d CH- (CH2) nCooh \u003d 8mno2 (s) + 2R-COOK + RCOOH + 3KOOC (CH2) NCOOK + 4H2O
Potassium permanganate is oxidized, while oleic acid contains C \u003d C, which can be used as a reducing agent, just like the potassium permanganate reacts with ethylene, oleic acid is oxidized into a smaller molecular weight acid, and controlling potassium permanganateIt is restored to manganese dioxide (as long as the solution is neutral, it can be achieved); oleic acid is also a dispersant. 8KMNO4 + 3R-CH \u003d CH- (CH2) nCooh \u003d 8mno2 (s) + 2R-COOK + RCOOH + 3KOOC (CH2) NCOOK + 4H2O
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8KMNO4 + 3R-CH \u003d CH- (CH2) nCooh \u003d
8mno2 (s) + 2R-COOK + RCOOH + 3KOOC (CH2) NCOOK + 4H2O
8KMNO4 + 3R-CH \u003d CH- (CH2) nCooh \u003d
8mno2 (s) + 2R-COOK + RCOOH + 3KOOC (CH2) NCOOK + 4H2O
More
VOTE