Why carbon-carbon triple bond can be oxidized by potassium permanganate Besides acetylene, why are the three bonds of other alkynes oxidized by potassium permanganate Thank you, God.

Why carbon-carbon triple bond can be oxidized by potassium permanganate Besides acetylene, why are the three bonds of other alkynes oxidized by potassium permanganate Thank you, God.

The carbon-carbon triple bond is an electron-rich group
And potassium permanganate has strong oxidation, that is, electronic ability
If the two meet, there will certainly be an oxidation reaction, producing CO2 and water

What is the equation for the oxidation of double bonds in potassium permanganate?

Olefins are divided into several cases:1. Two hydroxyl groups are respectively introduced into the double-bonded carbon of dilute cold potassium permanganate to form o-diol 2. High concentration or acidic potassium permanganate a. There is no substituent on the double-bonded carbon, i.e.=CH2, which is oxidized to CO2b. There is one substituent on the double-bonded carbon, i.e.=CHR, which is oxidized to carboxylic acid c. There are two substituents on the double-bonded carbon, i.e.=CR1R2, which is oxidized to ketone Both double-bonded carbon follow this rule, e.g. RCH=CH2, which is RCOOH and CO2, RCH=CHR, which is formed to form two carboxylic acids. Alkynes are similar to olefins. No substituent on α carbon forms CO 2, and substituent forms carboxylic acid.