Side Chain Oxidation of alkyl Benzene by DEY'S LEARNING for NEET, JEE (Mains & Advanced), BSc

[@d.34]

This is amazing video thank you sir

[@ruthhatanian2592]

Thank you so much for showing this mechanism. I searched for it for hours online and in many sources of literature. I finally found it here!

[@martinsvoboda9411]

Thank you very much for this mechanism !!! greetings from Poland.

[@manvikishore9187]

Ohh wow 😮😮

[@laiqzada8491]

@@manvikishore9187 Hi

[@laiqzada8491]

Hi

[@kaliraj8607]

I also mechanism got from new york

[@killerkhanop323]

Sir thank u sooooo much...
Mujhe ye wala reaction mechanism kahi se nhi mil rha tha.❤❤❤❤

[@bibekanandadas76]

Thank you so much sir......very helpful 😊

[@sonusuchitra]

You are the best teacher of organic chemistry please keep it sir

[@abdullahchandia]

Sir you are Great.
You taught very well.
I was searching that thing but I find here..
Thank you soo much..

[@rameshwarsharma1749]

Best explaination

[@Richmanluvsu]

This is the best to a full mechanism showing this everything else just shows the reagent thank you. What does the k+ mno3 charge become to verify if it follows valence rules?

[@khanmohammadtavassoli5363]

very good

[@amanshah9745]

Very helpful sir.

[@anupassi4770]

Thank you soo much sir. 😊

[@aarifbashir3721]

Sir my question is when we try to oxidize ethyl benzene it first forms phenyl ethanone . Now how can we oxidize this intermediate to benzoic acid. Eagerly waiting for your reply

[@Richmanluvsu]

My question too like if the rule is we only need one benzylic proton how are the carbon carbon bonds broken since deprotonation cannot occur

[@fatamistudio]

Nice

[@redmitest701]

Amazing where can i learn from you?

[@debojyotyghosh3187]

Sir, chinte parchen ... ami khuje khuje ber korlam, apnar ei channel, abar purano class gulor kotha mone pore jacche , pronam janben sir , valo thakun, subscribe kore rakhlam ....

[@ankitroy7761]

He didn't give a shit🤣🤣🤣

[@aryaop3796]

@@ankitroy7761 he doesn't need to he meets his old students periodically and what's your problem u are doing hate comments on his all videos if u don't like get lost u pubg freaks will never realise chemistry

[@toanngo3146]

Thanks very much

[@ankitroy7761]

Tooooo
Ab chem Olympiads ke liye taiyaar??

[@aryaop3796]

@@ankitroy7761 tu loafer hain kya ??

[@darkflinch5786]

Thank you very very much sir

[@killerkhanop323]

Keep uploading videos like that one...

[@pushpawaghe3138]

Please mechanics of :
From Benzaldehyde to Benzoic acid
Please....

[@mitchdevoight]

Sir. When you oxidised propylbenzene, one of the main product is benzoic acid. May i know what is the by product then?

[@DeysLearningChemistry]

The by-products may be ethanoic acid, propiophenone (benzoylethane) etc

[@blackspec1855]

Thank you sir

[@finknow3558]

Sir bhot dundhne ke bad mechanism pata chala hai

[@vanessaaitkensilva4279]

I've been looking for this mechanism for hours :C thank you so much!!!

[@ahilyakadam5658]

What happen if we take substituted toulene??
Like a orthochlorotiulene

[@redmitest701]

Sir do you provide personal guidance

[@naygle94]

Thank you sir,
Do you have reference paper for this machanism?

[@forouqam]

Thank you a lot of times 🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸🌸

[@chemistrywithshafaathussai7586]

A very informative lecture.....
Keep it up sir✌✌

[@shahfaisal4782]

v nice sir

[@nacl4299]

THank you Sir

[@tamalikamaulik9222]

Thanks sir

[@manpreetkaur-ji8tz]

if we don't add acid then what will be the product?

[@aneeshraam9568]

Primary alcohol will be formed

[@sameerk_28]

Thank you sir.

[@saikatdas6884]

Thank you sir ...it's very helpful .....🥰🥰

[@knowledgepoint6321]

Thanks

[@muhammadowais3230]

Great yr ❤

[@mrityunjayghosh275]

@@ankitroy7761 you get Lost

[@supriyaghosh7418]

We are missing your class 😢 so much sir

[@supriyaghosh7418]

Your teaching style is unique.

[@spm3847]

thankew sir

[@heysilvia]

That help me a lot. Thank you Dr.

[@DeysLearningChemistry]

Welcome

[@laiqzada8491]

Same here dear

[@priyalneekhra5418]

Why we used H3O+ then

[@DeysLearningChemistry]

In alkaline medium we get the salt of carboxylic acid i.e. carboxylate salt. On acidic work-up (addition of H3O+) protonation of carboxylate anion occurs and we get carboxylic acid.

[@kimyacabirhayyan3597]

Thanks..

[@Shreya_B_a_n_i_k]

Sir this question is from which chapter???

[@DeysLearningChemistry]

Hydrocarbons (Class 11) & Carboxylic acid (Class 12)

[@Shreya_B_a_n_i_k]

@@DeysLearningChemistry yes sir we have studied it in hcarbon just remembered

[@rameshwarsharma1749]

❤

[@doctortridivs144]

...,....Sir....,...

[@zaxmito2214]

😘😘😘

[@taraknathsaha67]

please give reference of this mechanism

[@DeysLearningChemistry]

Book of R.K.Kar

[@Varad-p7f]

My chem teacher while oxidation mechanism....
Beta. Aay lag jaati hai ab kaise jala ye mat pucho

[@forouqam]

So useful 😍

[@kidJEEindia]

Sir why only benzylic hydrogen will breake why not other hydrogen.plz sir clear it

[@DeysLearningChemistry]

Benzylic free radical is much more stable than other free radicals due to resonance involving the benzene ring.

[@kidJEEindia]

@@DeysLearningChemistry thank you so much sir..No one can teach like this.

[@shubhamraj11Nov]

Wrong mechanism

[@ankitroy7761]

Neem ta patta kadwa
Ye Sala bhadwa

[@manvikishore9187]

How

[@shubhamraj11Nov]

@@manvikishore9187 all chemistry scientists said that its reaction mechanism is not clear but this guy make forcing mechanism of this reaction.

[@snigdhamohapatra5053]

Thank you sir

[@bishnudalai]

Thank you sir