IITJEE. NEET Doubts forgot IIT, if you wanna get a decent college in India, you have to be expert in organic chemistry. They will ask the conversions involving multiple reactions
Potassium permanganate? More like potassium perfect-manganate! This was a wonderful video, and I learned so much; thank you for sharing your knowledge!
It's not fully understood and therefore, most professors don't require the mechanism for this reaction; however, because it's a commonly used reaction, they require you to know the product that is generated from a reaction with KMnO4.
Oxidation-Reduction reactions are very fast in nature which does not give us enough time to study the kinetics of the reaction and investigate its mechanism. We know the exact mechanism for very few oxidation reduction mechanisms.
Can you do examples with benzene substituents please? I understood everything in this video but the moment you add a substituent, I have a meltdown and panic attack followed by a straight-up girl fit
hi sir, i dont think one can consider a mirror plane as shown in the beginning of the video as cyclohexane exists in chair form and not planar form. cis 1,2 dihydroxy cyclohexane is disymmetric and hence chiral . However it exists as a non resolvable d-l pair since both isomers exists in an 1:1 enantiomeric excess . so it doesnt show a net optical activity ..
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Thank you! I’m passing year 1 University chemistry because if you 🙌🏽
we have to study all this in high school. I'm so tired honestly I'm gonna fail chemistry this year gaahhhh
We study this in high school in india lol
@@abhaykhatavakar757
Hahah, that is honestly insane. You're a champ.
@aozla hayka what?! No way. In India, we study this at 16 years old😳😳😳
IITJEE. NEET Doubts forgot IIT, if you wanna get a decent college in India, you have to be expert in organic chemistry. They will ask the conversions involving multiple reactions
Potassium permanganate? More like potassium perfect-manganate! This was a wonderful video, and I learned so much; thank you for sharing your knowledge!
How come no-one ever shows the actual mechanism invloved for this reaction?
It's not fully understood and therefore, most professors don't require the mechanism for this reaction; however, because it's a commonly used reaction, they require you to know the product that is generated from a reaction with KMnO4.
Oxidation-Reduction reactions are very fast in nature which does not give us enough time to study the kinetics of the reaction and investigate its mechanism. We know the exact mechanism for very few oxidation reduction mechanisms.
I though it was only me who has this question
I have it . Do you want it ???
How I wish there was a repost button so I could repost this question. Because I was about asking..
very helpful for indians senior secondary students and jee aspirants.
Jee ka prep kaisa ja raha he?
@@sandeep7973 acha chal rha h
Rishi Raj physics ke liye koi ache RUclipsrs suggest kar sakta he kya? Physics wallah ke alawa
@@sandeep7973 physics wallah, concept acche se clear kr sakte hai
Rishi Raj uske alawa? Kyuki uske videos bohot lambe he
Thanks
I got my doubts clarified in the last 3 minutes of this video ;) ( 8:09 )
Currently in 11th grade studying for JEE, and it makes me realize how difficult our course is as almost all my resources are university courses
This guy teaches way better than my school teacher.
Perfect video! Thanks for explaining the stereochemistry along the way.
Hey peyton
ਸੁਚਾਰੂ ਢੰਗ ਨਾਲ ਸਮਝਾਇਆ
IIT JEE students , where you at ? ;)
Wow so exceedingly clear and helpful. Thank you!
Sitting paying attention drawing everything and then
2:44
4:00
BOOM OH from KMNO4
It's not OH from KMnO4 dummy
Great.. Thanks Prof. from my deep heart..
Thks it helped me in jee
U cleared jee mains jan ? How was the paper in jan
THE ORGANIC CHEMISTRY TUTOR🤛
Thank u so much. Your videos r very helpful and easy to understand
My fav tutooorrrr
Thank u so much.. it helped a lot
You explained so well as explained by MIT prof. Because I have passed through MIT and I am an software developer
Your English sucks
How did you excel at that SAT with English this horrible?
Really, bro I don't think so
Ha ha
I see we have the nice people of the RUclips Comment section here
Guys he must be talking about Manipal
I owe you a lot🙌
THANK YOU VERY VERY VERY MUCH
Can you do examples with benzene substituents please? I understood everything in this video but the moment you add a substituent, I have a meltdown and panic attack followed by a straight-up girl fit
A bit late but in those cases I believe KMnO4 reacts like an oxidizer and grab’s electrons
What if the reaction is to be held in acid conditions .??! (reaction of alkene with KMnO4 under {H+})
He starts talking about acidic conditions at 8:15. H3O+ is the same as H+ =)
Precise points gvn..
شكراً جزيلاً
Thank fuck for the mechanism cause I was close to a mental breakdown
sir so can we say , conc kmno4 behaves like oxidative ozonolysis reaction under acidic medium ?
2-methyl-2-butene in KMnO4,OH- cold will be what
Thank you
hi sir, i dont think one can consider a mirror plane as shown in the beginning of the video as cyclohexane exists in chair form and not planar form. cis 1,2 dihydroxy cyclohexane is disymmetric and hence chiral . However it exists as a non resolvable d-l pair since both isomers exists in an 1:1 enantiomeric excess . so it doesnt show a net optical activity ..
What about under neutral conditions?
where can i find reaction with OsO4
It is shown
Does potassium permangenat react with ether?
At 7:35 shouldn't the methyl group be oxidized to carboxylic acid too. Or does it only happen in benzene only.
Only carbons with the pie bond will be oxidised, just remember this because chem was never really my main subject.
Happens with benzene derivates only (side chain oxidation)
How KMnO4 goes to MnO2, in my reaction it is going to MnO3H
Oliver Road
So how will you draw the seperated structure?
What about oxidation of Alcohol in Neutral Medium
Aldehyde forms
ily
Great
87401 Cronin Greens
What is difference between product of acetylene kmno4 and normal kmno4
8:10
does anyone have an arrow push link for the last problem