Final Exams and Video Playlists: www.video-tutor.net/

Thank you! Thank you! Thank you! Your videos are to the point and you explain things so well!

Your videos are super super useful. Thanks!

who is else here is studying pharmacy and regretting it with his/her life ? 👋🏻

@subconsciousmerchant4332

4 жыл бұрын

Pharmacy is love 😒

@aymenbourefis9146

3 жыл бұрын

The struggle is real , tho , pharma forever 🙋🏻‍♂️❤️

@atikamochi9760

3 жыл бұрын

I'm not regret, 😂

@abramsavantp.ybanez8302

2 жыл бұрын

loving it so far org chem is currently my fav sub ♥

@hiluti9482

2 жыл бұрын

Here🤞😭😭😭

Awesome, say thanks will be never enough to show you how much you helped me , Thanks anyway

Brilliant video, thank you

Thank you once again.

You are an excellent teacher. Physical science is not my thing and you are explaining things perfectly to this biologist!

Very good, thanks ❤️❤️

Amazing...you're amazing

you the giant organic person

How come for the first rxn with Bromination he didnt write the final product. Isnt it a benzene ring with with bromide attached plus FeBr3 plus HBr????

UNZA pharmacist here ❤ Enjoying the chemistry

Ver well explained

Thank you so much

Amazing

Am a teacher student teacher sir and I wish you could be my mentor teacher ; you are perfect

Aromatic halogenation mechanism? More like "Amazing organic chemistry instruction!" Thanks again so much for making all these videos.

Thanks 👦🏻👍🏼

Thannnxxx,, i really appreciate it

As a Neet Aspirant , this video is gorgeously knowledgeable 🌹❣️ Will now onwards watch ur video to grab more of the Organic Knowledge from u sir 🌹 Lots of Love from India🇮🇳

@PunmasterSTP

Жыл бұрын

Did you already take the Neet, and if so, how'd it go?

@priyamkamdar1056

9 ай бұрын

tf is "gorgeously" knowledgable bruh

Is this reaction the same in all other aromatic compounds plz?

What will happen if we use for example, HBr instead of Br2?

@fatcammal

5 жыл бұрын

you combust

Can we call this as the first mechanism of halogen?

thanks man

10Q very much!

I don’t understand the step where the Nucleophile ( the aromatic ring ) attacks the Electrophile ( Cl +). Why does the second carbon that forms the pi bond get the carbocation charge ? Help me please I’m slow I’m learning but this is very interesting. Chemistry might just be my favourite science

@VenuGopal-js1qu

Жыл бұрын

there the c atom has 3 valencies occupied,but being tetravalent it gets a + charge as the c atom above it gets chlorine so it breaks the pi bond with lower c atom

Your naming is OK thanks

How do you know which carbon on the benzene ring to add the bromine to?

@tom_winguill

3 жыл бұрын

any carbon

@victorsahagun9997

3 жыл бұрын

@@tom_winguill what if there are substituents on the ring? Or if two rings are connected

@tom_winguill

3 жыл бұрын

@@victorsahagun9997 as bromine is an electro negetive atom it selects the cabon with high electro positive character

@ishaankapil4982

2 жыл бұрын

@@victorsahagun9997Principle of directive influence will take place, if there is +I-Group, an electron donating group on benzene prior to Br, then due to resonance negative charge is created on ortho and para position of benzene and here Br is behaving like electrophile ( a positive chaged ion) and Br will attack on Ortho and Para Position of Benzene ring. And 1-bromo-2-nitro-benzene and 1-bromo-4-nitro-benzene is formed. And if their is a presence of negative-I Group like NO2, which is electron withdrawing group, created positive charge on Ortho and Para Position and as I said, here Br is behaving like electrophile not like electronegative atom, it will get repulsion from Ortho and Para position and attack on Meta position which is more electron rich as compared to Ortho and Para position, hence 1- Bromo-3-nitro- Benzene is formed.

@ishaankapil4982

2 жыл бұрын

@@tom_winguill No here Br is behaving like electrophile a positive charged ion, electronegativity of Br is seen when it is bonded with some other element than Br itself...

Do you have videos on polybromination? Or ortho-meta-para directors?

@jameson1239

4 ай бұрын

A bit late but a general rule is electron donators activate the Ortho and Para positions and electron withdrawing groups activate the Meta positions the only real exception is Halogens which activate the Ortho and Para positions while being electron withdrawing groups

Veeeeeeeeeeeeeryyyyyyyy useful

Can you do one for Fluorination? Please!!

@ishaankapil4982

2 жыл бұрын

Flourination is not possible...

@jameson1239

4 ай бұрын

The only real way to add a fluorine is by using HNO2 and HBF4 direct fluorinations are explosive

Why is the compound unstable

JG 🖤

Schools and lessons are god damn boring. It just Rob happiness

Toluene + Br2/FeBr3 , Ortho or Para

From Bangladesh ❤

I’m waiting to see if we writing Cambridge

@bignono2439

3 ай бұрын

Did you?

@jvstRuee

3 ай бұрын

@@bignono2439 Yeah, we did

Does anyone else think he kind of sounds like Mark Wahlberg?

@PunmasterSTP

Жыл бұрын

Yes, I do too.

In iodination, what's the role of the acid H2SO4??

@tom_winguill

3 жыл бұрын

catalyst

@rockypop9506

3 жыл бұрын

Yea catalyst

Why is iodination far simpler than the other two? It's as if a solvent isn't used

Wait who are you?

yawa wala gihapon ko kasabot

@abramsavantp.ybanez8302

2 жыл бұрын

balik balikaa HAHAHAHAH

This cyclic compund isn't activated And u didn't explain the reversibility part of iodination Waste of time