September 28, 2020, 05:14:35 PM
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Topic: protonolysis of organoborane  (Read 74 times)

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Offline sayantan dutta

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protonolysis of organoborane
« on: September 13, 2020, 04:39:25 PM »
protonolysis of organoborane is done by acetic acid...but same thing can't be done  mineral acid like hcl h2so4 ..why ??? usually basic oxygen portion of acetic acid cordinate with boron . helping to increase the acidity of hydrogen to liberate more.....if that so same thing can also occur by hcl..where cl- cordinate with boron and thae alkyl group breaks and capture the hydrogen proton...but it won't occur???

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