Oxidation of Alcohols: Primary, Secondary and Tertiary
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- Опубліковано 8 вер 2024
- Primary Alcohol to Aldehyde, then Carboxylic Acid
Secondary Alcohol to Ketone
Tertiary Alcohol NO REACTION.
Oxidation is usually with potassium dichromate solution, which turns from orange to green if there's a reaction. Heat (reflux) is helpful.
You can stop the reaction at aldehyde by using "distillation".
I thought I'm stupid for not understanding how do two H-s become a second bond and you just proved it's not me. Thank you so much sir.
This was truly an incredible video. Every other video I’ve watched on this topic has been very confusing, but I understood everything you said, and it was a very short video! Thank you so much Nate!
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I usually don’t comment on videos like this, but this was very well done and easy to understand
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I liked your explanation. Thanks a lot!
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Just wanted to know why tertiary alcohols do not oxidise..And see..I found the perfect answer!!!
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This saved me so much time
What about the popoff's rule of further oxidation of ketone group into 2 carboxylic acids..upon reacting it with strong oxidising agent..Why is it not applicable here...according to popoff's rule,,,the ketone should further convert to 2 carboxylic acids
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Could you make a video on Naming of Amine???
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so if it’s tertiary it automatically doesn’t have a reaction?
Yes that it
For any condition?
Very helpful thanks
But in my text book it is given that tertiary alcohol also shows oxidising properties it converts into acetone and then acidic acid.... Plz reply what's going on
You cannot oxidize tertiary alcohols as the carbon attached to the OH group (known as carbinol) doesn't carry any hydrogen atoms to be oxidized ..
Nourhan Ashraf .....thanks
You're welcome 😊
In 4 min
That's what I want just an hour before my exam
Can you please do a video on acidity of alcohols and phenols?? please..
Hello sir you help me a lot ❤️
But do you have an example in this but in Cyclo I'm having a hard time to understand it.
thanks sir '
Helpful. Thx
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From we can find out complete mechanism
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Why is sulphuric acid not used in reaction of alcohol with potassium iodide ?
What do we call an alcohol like methanol, which doesn't have another carbon ? Is it still primary ?
Sir please make videos on amines
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primary is prop
secondary and tertiary are but.....right?
Thankyouu!
Thank You. SO HELPFUL
A level chem is overwhelming
Until now I always just thought Tom cruise was just a pretty face
Not being rude but I think primary alcohol should’ve one methyl but your primary is like methyl alcohol
Is the Cr2O72- oxidised or reduced?
This helped some, though I wish you'd distinguish between mild and complete oxidation :p
If your formula doesn't have arrows, it's not a mechanism
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Thank you