Oxidation of Alkenes Using Potassium Permanganate (Hot and Cold Conditions)
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- เผยแพร่เมื่อ 20 ต.ค. 2024
- We've seen that KMnO4 can oxidize alcohols and aldehydes to give carboxylic acids and ketones, but this reagent can also oxidize alkenes. The product(s) will be different depending on whether we use cold basic conditions or hot acidic conditions, so let's see what happens in both cases!
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Always the best explanations are found in your channel.You're doing a great job by helping many.
Are you a human? You know all types of chemistry,maths,all biology,physics and manu other things-for me is hard to catch one :))
Potassium permanganate? More like "I think everyone here would agree these videos are great!" Thanks again so much for making and sharing all of them.
Dave is always there for our rescue 🌟.
I always find answers to my questions in your lectures.
Best explanation ❣️
Love from India ❣️
Very Informative and enjoyable video, Thanks Prof. Dave
Hey Dave. Thanks for these videos. Youve been tremendously helpful during all my undergrad science classes.
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I love these OC guides, they are so informational!
Took this test two weeks ago! But still helpful! More organic 2 and physics 2 videos please please!
Did you take any more ochem since then, and if so, how'd it go?
Thanks for the video. I couldn't distinguish between cold and hot Kmno4 reactions
Very informative. Explained so well ❤
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Dave knows
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a really good explanation
Thanks sir....love from India
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How'd they go?
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So, why the vicinal diol didn't get oxidised further.. as.. kmo4 is still there..??by the way.. nice explanation.
Is the KMnO4 alkaline or acidified in cold conditions? Oh and rest of the video and the way you explained this is absolutely brilliant. Nice:)
You're always the best one to clear all my doubts. Thank you so much
Gave a like just into your intro❤😍
hey dave! great videos, very helpful!
when talking about the secondary carbons, you said in the first step, that both bonds (sigma and pi) would be cleaved. But afterwards you said that permanganate can not break a carbon-carbon bond. Why is that so?
I suspect that it has something to do with the newly formed carbonyl, is that right?
ps: i would appreciate a knoevenagel-video
i love this man
Isnt there a way to use periodate and wind up at the aldehyde?
Ok it’s been a while. You chopped your locks!
Thanks prof!
Your side notes for different degrees of carbon which converted to 3 different molecules do not match your examples. Can you fix them in the comments? (Ex: secondary becomes ketones not carboxylic acid)
would a single methyl substituent cyclohexene produce a ketone and Carboxylic acid
This topic is of which standard??😕
wont we use cold dilute "acidified" kmno4?
just if you make longer videos 🥺😭
Thnx sir ❤
Can anyone tell me where OsO4 was discussed?
thank youuuuuu
Professor Dave? More like Professor Babe 🤤
I appreciate that humor!
Excuse me, do you know how to prepare silica gel to absorb moisture or silica gel to act as the stationary phase in thin layer chromatography.
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THE HAIR. His glorious hair 😭
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Is it true you're not a professor?
Nope. Try to avoid listening to lying con men.
@@ProfessorDaveExplains Whoa you believe that professors are lying con men?
No, I'm saying that people like to slander me, mainly due to my efforts debunking pseudoscience.
Never mind, I got my answer. It was mentioned in the video haha.
What happened to the hairs
Some organic chemistry happened and he got that fresh cut
@@akshit0203 😂 ty ty. I honestly don't even remember making that comment lol
thanks :)
Organic chemistry is a nightmare for me.
I got it 🎉
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