Oxidation of Alcohols: Primary, Secondary and Tertiary

[@vanyiandras3041]

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.

[@radparkourdude3604]

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!

[@skyblizter]

this person only use a paper and a marker to teach us,thank you sir

[@tamerfarhat5042]

This is perfection. You totally deserved my like.

[@Prettyfantacy]

Please do more videos you are the best and we students find these videos so helpful because our teachers are not that great

[@emmanuellaaadickson]

This is amazing! Omg like yo I don’t understand how well you just taught that!

[@n1ggesa]

Yooo I swear no cap . This guy just so easily nd humbly taught us like if it's a piece of cake 😂

[@theplantslant2431]

I usually don’t comment on videos like this, but this was very well done and easy to understand

[@alejumayao]

As a first year med student, I greatly appreciate you

[@بولاريسنجمالشمال]

I am a med student in the first year. thanks for all your help and I hope you have a great day❤️

[@scarlie8365]

youtube doesn't have a double-liking feature but i would have clicked it for this explanation, thank you :)

[@AT-sk7nm]

FINALLY A VIDEO I CAN ACTUALLY UNDERSTAND. I was about to cry 😂

[@eldraco252]

thank you so so much, other videos over complicate the process and make it hard for young students to grasp the essence. thanks for being direct

[@marvysandrae.bongolto5075]

you are a life saver thank you so much

[@kb3239]

Thanks!

[@thebharatswabhiman4707]

Just wanted to know why tertiary alcohols do not oxidise..And see..I found the perfect answer!!!

[@tainaradesa5817]

I liked your explanation. Thanks a lot!

[@u_kno_deweiv1744]

Oh my god have I just found Jesus

[@mirrormaster5874]

ifkr

[@nexusbane8801]

How was it?

[@tasneem6427]

You are incredible.just wow 🤩

[@nurinfitra2458]

u deserve a whole lot more views sir

[@mk2103.]

Thanks man! Very informative and to the point video! Keep it up!

[@shortsrajeshkumar5663]

Thanku Sir very much for clear my doughts

[@alancummings5651]

Excellent explanation

[@khushirajoria9836]

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

[@itsucksfr]

you really are a hero :heart:

[@nanajuma7959]

Love this simple and amazing video of chem

[@mirrormaster5874]

you are heaven sent

[@azizaahmed1521]

Tomorrow is my organic chemistry exam😥😣...

[@BlazedCLS]

aiza ahmed goodluck 😘

[@deepmeyt]

Same here😂

[@rosendjavera7734]

Mine is tomorrow 😌

[@uejai8302]

OMG tomorrow is my presentation, and you save me！！！！thank you so much for sharing

[@ParaREZX]

How'd it go?

[@captainvenom7252]

In 4 min That's what I want just an hour before my exam

[@zainabayadalwali5231]

thank you

[@pawanprakash4131]

Could you make a video on Naming of Amine???

[@lachlanbunyan6445]

Thanks bud, much appreciated video!

[@SZ-mc7ch]

This saved me so much time

[@fagunichowdhury8033]

Hiii sir I m frm india watching ur video..

[@pranitauprale8099]

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

[@nourhanashraf2653]

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 ..

[@pranitauprale8099]

Nourhan Ashraf .....thanks

[@nourhanashraf2653]

You're welcome 😊

[@uyujooseyo]

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.

[@bhavaniselvam4393]

Can you please do a video on acidity of alcohols and phenols?? please..

[@mysterygirl4797]

so if it’s tertiary it automatically doesn’t have a reaction?

[@叶默-i4o]

Yes that it

[@samkelenibe2018]

For any condition?

[@Kris-rg6yv]

You rock. Seriously.

[@nyawirawaithaka4993]

Thank you!

[@abhishekpawar5791]

Why is sulphuric acid not used in reaction of alcohol with potassium iodide ?

[@rorimakaleng6295]

What do we call an alcohol like methanol, which doesn't have another carbon ? Is it still primary ?

[@kasaneshayalew5431]

You help me so thank you

[@Uzairali123456789]

I love this guy

[@Lawofattractionandbeliefs]

saved my life !!!

[@kaivanshah4304]

amazing 👍👍👍👍👍😊😊

[@aquiiprime5614]

thanks sir '

[@nicholaswestwood5791]

Very helpful thanks

[@nursepotassium]

primary is prop secondary and tertiary are but.....right?

[@hermellategegne1392]

Godbless you

[@tinotendachibvuri9267]

Helpful. Thx

[@viiperbiite]

Is the Cr2O72- oxidised or reduced?

[@nguyenbichvan1532]

loved it!

[@abhiacharya7377]

Thanks man

[@akmalhakim286]

Not being rude but I think primary alcohol should’ve one methyl but your primary is like methyl alcohol

[@yadavsurinder4646]

Sir please make videos on amines

[@laurengittecolgan3238]

THANK YOU!!!!

[@abdurrazaq3657]

From we can find out complete mechanism

[@preetamvyawahare1244]

very good

[@finickytaint3400]

Until now I always just thought Tom cruise was just a pretty face

[@zebroar4630]

Thanks man!

[@trigobrooken6260]

A level chem is overwhelming

[@kelumrajakaruna3928]

thats grate :)

[@emmanuel.m.4987]

If your formula doesn't have arrows, it's not a mechanism

[@amahlemasondo7857]

Thank You. SO HELPFUL

[@areebaqamar942]

Thankyouu!

[@Yoishmeh]

Sheldon?!

[@thusharanup4906]

godsend

[@kawtharbakhach5848]

This helped some, though I wish you'd distinguish between mild and complete oxidation :p

[@viiperbiite]

*_TERSHERIARY_*

[@melikasalehi2551]

I think I love you, like where have you been all my life???

[@adarshentrepreneur2505]

jhhhatu ho salkeeeeeeeee

[@iamsugoi2779]

thank you

[@oswin4715]

Thank you