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@9ball253 жыл бұрын
zoned out of my three hour class and had no idea what was going on. Watched this 12 min video in class and now I'm ahead of everyone.
@lmthagod328 Жыл бұрын
I swear most organic chemistry lectures are never understandable 😂
@kylet6612 Жыл бұрын
Yes you are correct! My teacher does not teach in organized way. We learn simple concepts but given advanced problems lol
@jul2447 Жыл бұрын
@@lmthagod328 😭
@krazykanpuriya Жыл бұрын
@@kylet6612My teacher too is like that 😭. Proof that we all live the same life 😂.
@raghunandanbs20059 ай бұрын
3 hours I've been zoning out my whole college life , lyf sucks for me .
@GurleenKaur-xy6xv8 ай бұрын
not sure how my professors make it so complicated when you can clearly explain it to us in such clarity
@galyavakian2 жыл бұрын
I think you will save my life for my medical school entrance exam!! I really struggled in Organic Chemistry during finals!
@domoo26392 жыл бұрын
Listen i am struggling. Chemistry was never my strongest science ! and i need this class to stay in my nursing program !
@maximilianavila75102 жыл бұрын
@@domoo2639 hope you succeed!
@advayargade7462 жыл бұрын
Thanks for clearly explaining the nooks and corners which are not that commonly taught. Really helpful!
@ezaaax811 Жыл бұрын
Lmaoo sameeeee 😂😂😂
@snazzyratking64666 ай бұрын
Oh my gosh I’ve been looking for the fluorine example everywhere! Thanks for explaining!
@charlykhalil1283 жыл бұрын
Best Organic Chemistry Tutor EVERRRRR! I love u man! I salute you!
@aliciapark523 Жыл бұрын
So simple and straight to the point!
@frhneil14633 жыл бұрын
hello sir, i'm wondering what it's take and how long it's take for you to understand this stuff let along teach it clearly in the most simple way ever? I'm amazed. I want to understand stuff till I can explain it just like you did.
@coolspike76592 жыл бұрын
You will, The key is to NEVER GIVE UP !!! You are capable of doing what he does, and so much more !!
@Mirwhosane Жыл бұрын
Hi
@jewelokwuosa94135 жыл бұрын
Thank's so much! quiz on this tomorrow, really helped : )
@alessiailas49292 жыл бұрын
Same here now and it's midnight 😭
@jewelokwuosa94132 жыл бұрын
@@alessiailas4929 good luck!
@carolo6098 Жыл бұрын
@@alessiailas4929 1am 😅
@atharvmathur912 жыл бұрын
Thank you soo much helped me a lot for my 12th grade exams😀
@grapesjuice68602 ай бұрын
I pray for this man alot
@akashprofile Жыл бұрын
A lot of thanks, Brother! You cleared my prolong confusion.
@shaghaieghtaheria94533 жыл бұрын
I owe my life to you sir,
@Ankitshbj10 ай бұрын
Any JEE/NEET aspirant☝️☝️☝️
@advaitkolhe81643 ай бұрын
Haa bhai, JEE 2025. Halo arenes and amines ke PYQ me bohot use hota hai E2 mechanism
@nikodg1945 жыл бұрын
The reason why the Hoffman product forms while e2 elimination of fluorine is due to enthalpy of the fluorine carbon and that's why it dont want to go easily at least that's what my profesor says
@jellyfam11972 жыл бұрын
I have two orgo professors both highly respected in their fields, both had different reasoning. Consensus is that no one exactly knows, there’s 2-3 hypotheses as to why Fl- is Hoffman
@lizareizis25172 жыл бұрын
what makes a good or bad leaving group?
@JamesKing-pl2xu2 жыл бұрын
The size i believe because its size is what determines the polarizability (ability to stabilize the charge). Therefore I- or Br- are better leaving groups than say F- and Cl-
@rohankrishna92284 жыл бұрын
Its excellent sir I learned a lot thank you so much sir
@alondraherrera41702 жыл бұрын
didnt really explain what an e2 reaction is and how it works, do you have a video on that?
@user-xh5eg6fi5m11 ай бұрын
Thanks alot all my doubts is now cleared 😊
@Whoooooo_tao27 күн бұрын
Dude saved my finals for the 5th time
@uthpalp38076 жыл бұрын
Helped a lot.. thanks
@user-zt4qr7mz4f2 жыл бұрын
You're a lifesaver
@yuridanylko Жыл бұрын
Say there is a molecule (a triene) in which a bulky base is used to to create a hoffman product via an E2 reaction. The first option will result in a cis disibstituted pi bond. The second option will result in a geminal disubstituted pi bond. There is also a trisubstituted pi bond possible towarss the middle of the alkene. Will the major product be the cis or geminal alkene? What drives this? Stability of the carbocathion? Steric hindrance? Stability of the end product?
@Hrishikesh..000 Жыл бұрын
Thank you bro Have a great day....
@sakshamshrivastava4221Ай бұрын
All doubt clear sir thnks❤
@user-qd1mz3qn9t Жыл бұрын
You are the BEST ! Thank you very much !
@jesusmrosario-claudio41043 жыл бұрын
Thank you once again.
@albertlee858610 ай бұрын
If E2 is favored with a polar aprotic solvent is there a reason you use methanol for many of the solvent examples? Thanks for the video, super helpful for a quick MCAT review! Edit: type
@annablueseas10 ай бұрын
i was thinking the same thing! i was so confused
@shaktisinghhemant19372 жыл бұрын
Thank you so much
@ilickcatnip3 жыл бұрын
Great explanation!
@caloman51912 жыл бұрын
super helpful.
@bobu5213 Жыл бұрын
So in both the E1 and E2 reactions, both the minor and major product always form if possible?
@muslimgirl1481 Жыл бұрын
Yes bcz both are regioselective ( can give major and minor products) and sterioselective ( can form cis and trans product) also.
@puneetgill40643 жыл бұрын
for -O-CH(CH)3, will its preference be 1>2>3 because of steric hindrance?
@maureene71383 жыл бұрын
It will actually prefer 3>2>1 for E2 and E1
@xxcoltonxx254010 ай бұрын
What about when its an alkyl group connected to a benzene ring, kinda need to know how to find the minor product there don't we....
@David-fh6rr6 жыл бұрын
But why does is the conjugated product formed? The MeO- doesn't know it has to make the conjugated product, it has no brain. Does the double bond already draw electron density from the a-CH bond to make it more likely to break before it happens?
@ashueje64162 жыл бұрын
Both the products are formed in the reaction the conjugated diene is majorly formed as it is more stable . the reactions occus so as the products have a lower Potential energy than the reactants is their is reconance then the stability of the alkene is more so this is the only reason why a cinjugated di ene is formed in major.
@carlovaldes2595 жыл бұрын
Thanks !!!
@theg.o.a.t10142 жыл бұрын
Now I am maestro after 12min watching
@kraken61619 ай бұрын
now is hoffman product the minor or the major because once the minor was hoffman then the major was hoffman
@sakshamshrivastava4221Ай бұрын
Thank sir
@Dr.DiMiTri.710 Жыл бұрын
You are officially the final evolution of Bill Nye
@KshitijPunani6 ай бұрын
Thanks nro
@FBR21694 жыл бұрын
6:22 why is the major product Hoffman????
@jadesamanta77174 жыл бұрын
The big, bulky base (tert-butoxide) cannot penetrate into the center of the molecule to deprotonate those Hydrogens (remember, the space-filling model: those electron clouds in the middle carbons are large). So, the only H the base can reach are the terminal ones on the end. Therefore, the Hoffman product forms, even though its technically less stable than Zaitsev. It is the only E2 reaction that can feasibly take place there.