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Пікірлер
@BrIndustries459 14 сағат бұрын
Damn. I wish I could attain one of your lectures
@selenagomez1624 15 сағат бұрын
Loved this video, so helpful!!
@duykhiem-vtr Күн бұрын
If we use the tertiary alcohol, is there a competitive reaction that leads to an exocyclic double bond, which is also a trisubstituted alkene?
@VictortheOrganicChemistryTutor Күн бұрын
Absolutely. Within the scope of the reactions we cover in an intro organic chemistry course, there are not many methods we can use to improve the selectivity here. The bond in the ring is a smidge more stable, so it would still be a major-ish product.
@duykhiem-vtr Күн бұрын
@VictortheOrganicChemistryTutor hi, so why an endocyclic alkene is more stable than the exocyclic?
@TimesLess-xc5zt Күн бұрын
It really helps me out for my exam prep ! ❤
@VictortheOrganicChemistryTutor Күн бұрын
Glad you find it helpful! Good luck with the exam!
@triple_gem_shining Күн бұрын
I actually really like the epoxide one. But thr ketone path is probably easier to see on a test
@VictortheOrganicChemistryTutor Күн бұрын
That's why I try to show different methods to help broaden one's synthetic horizons, so to speak.
@jennifermodise-db7uh Күн бұрын
Thank you so much this has helped. I like your accent!!!
@VictortheOrganicChemistryTutor Күн бұрын
haha Thanks! I'm glad you find my videos helpful.
@TimesLess-xc5zt Күн бұрын
KMnO4 used in OH- acts as a strong reducing agent
@VictortheOrganicChemistryTutor Күн бұрын
I’m gonna keep staring at you till you come to your senses 👀
@arnavsharma-lm5qm Күн бұрын
thanks a lot!!!!! this has really helped me!! wish me luck for my exam again!
@VictortheOrganicChemistryTutor Күн бұрын
You’re very welcome! Best of luck on your exam!
@arnavsharma-lm5qm 21 сағат бұрын
@@VictortheOrganicChemistryTutor thanks sir!
@maholog6357 2 күн бұрын
Adamsın
@hadeelmassarwa 2 күн бұрын
Thank you so much for providing a helpful and easy explanation!
@VictortheOrganicChemistryTutor Күн бұрын
You're very welcome! A lot of students struggle with thermodynamic vs kinetic control. Plus, there's a lot of bad info out there, so hopefully, this video helps students to get a better grip on it.
@BrIndustries459 2 күн бұрын
The Grignard reagents I see are always with Br is there a reason why Br is chosen over other halogens ?
@VictortheOrganicChemistryTutor 2 күн бұрын
Bromides are more reactive with Mg than chlorides and make Grignard easier to make with them. Iodides would be even better but making organic iodides is harder. So RBr is the golden middle-reactive enough and easy to make.
@fatmaelsayed8933 2 күн бұрын
thanks a million
@VictortheOrganicChemistryTutor 2 күн бұрын
You’re very welcome! Glad it helped.
@Fixprice-i2x 3 күн бұрын
мужик прорешал каждое задание с тобой, спасибо за помощь в подготовке!
@VictortheOrganicChemistryTutor 3 күн бұрын
Удачи на экзамене 👍
@theweeknd8087 3 күн бұрын
teacher you will literally save my life in the tomorrow exam, many many thnx
@VictortheOrganicChemistryTutor 3 күн бұрын
Haha thanks! Best of luck in the test!
@katherinebabalola4669 3 күн бұрын
I agree, the one with ketone looks more straightforward
@VictortheOrganicChemistryTutor Күн бұрын
I dunno why students hate epoxides so much lol 😆
@zulqarnainchaughtai 3 күн бұрын
Hi! Can leaving group determine the mechanism of the reaction? My High school book says if there is tosylate as LG then elimination is favoured and substitution is favoured if bromine is present as a LG.I have asked this question earlier and you promised to make a video on this issue😊
@VictortheOrganicChemistryTutor 3 күн бұрын
As I said before, no, leaving group by itself cannot determine the mechanism of the reaction.
@zulqarnainchaughtai 3 күн бұрын
@VictortheOrganicChemistryTutor thank for responding.
@pspv927 3 күн бұрын
ur saving my whole class with chem ty from my class and me
@pspv927 3 күн бұрын
if ur wondering its bc of the complex substituents vid my chem teacher suddenly said its in the syllabus our exam is tmr so ye found ur channel and its helping us a lot with our organic chemistry
@VictortheOrganicChemistryTutor 3 күн бұрын
Haha you’re welcome! Best of luck on the test!
@pspv927 4 күн бұрын
This vid was amazing ty
@ZohraFerdousseSifi 4 күн бұрын
but in the exam if they give us a molecule and tell us to represent it in cram projection ( dashes , wedges ) there's many versions depending how am seeing the molecule as u showed it in rotations part which one of them i should choose ? thanks for the video
@VictortheOrganicChemistryTutor 4 күн бұрын
That’s when you need to use your judgement and see what’s the best representation for a given situation. There’s no “one answer fits all” solutions in organic chemistry. Especially, when it comes to something like various representations.
@ZohraFerdousseSifi 4 күн бұрын
@@VictortheOrganicChemistryTutor got it , thanks a lot !!!
@BrIndustries459 4 күн бұрын
Nah the one with the ketone is much more easy
@VictortheOrganicChemistryTutor 4 күн бұрын
If you insist 😆 While we’re in the intermission between the semesters, I’m planning on a few more quick synthesis challenges and a few mechanisms.
@BrIndustries459 4 күн бұрын
@VictortheOrganicChemistryTutor that will be highly appreciated 👍
@pspv927 3 күн бұрын
@@VictortheOrganicChemistryTutor umm are you doing online classes or just yt vids?
@pspv927 3 күн бұрын
oh mb just saw the link
@theweeknd8087 4 күн бұрын
teacher please come in our university to teach real organic chemistry!
@VictortheOrganicChemistryTutor 4 күн бұрын
Haha nah! I better make more videos for everyone to watch and learn 😀
@siriluckponyam9631 4 күн бұрын
May I know if the formula can be applied for the NMR spectra for aromatic rings as well ?
@indiaseye7361 7 күн бұрын
Sir I am an student preparing for JEE examination. Helped me to clear concepts a lot and stronger my organic chemistry
@VictortheOrganicChemistryTutor Күн бұрын
Resonance is definitely one of the important concepts in Organic Chemistry, keep studying!
@ranaaymann1 7 күн бұрын
Great video
@physicsislobe 7 күн бұрын
Alcoholic koh??
@Chemistry_0908 8 күн бұрын
can you be my coach
@luciomagno6195 9 күн бұрын
When searching for tosyl the only image that appears is with the oxygen
@VictortheOrganicChemistryTutor 9 күн бұрын
I dunno what you're searching, but literally the first hit on google that I see is the wikipedia entry on the tosyl group. en.wikipedia.org/wiki/Tosyl_group Which also points the difference between tosyl and tosylate, which are not the same thing.
@LubeIn 9 күн бұрын
If we use something like NaOH then we can add the Ts group?
@BrIndustries459 9 күн бұрын
Organic chemistry is really weird. But i like it
@samaaahmed6619 9 күн бұрын
7:15 why in chiral center with oh is R .. With atomic priority Oh ...1 CH BR CH3 ....2 CH2 CH3 ....3 H ...4 SO IT IS CONTER CLOCKWISE,SO should be s .....?
@VictortheOrganicChemistryTutor 9 күн бұрын
And where exactly is the lowest priority? Is it looking at the observer or is it looking away from the observer? You might wanna review the assignment rules again 😉
@hammerff827 10 күн бұрын
Thnks sir😊
@vladmirputinpr 10 күн бұрын
Your videos are always amazing making everyone like the chemistry!
@subhekchasharma2537 11 күн бұрын
How to estimate products of pyrolysis
@european-rebel 11 күн бұрын
spasibo (mozhe buty d´iakuju)!
@MANDARx_2 11 күн бұрын
Matched all
@الواثقةباللَّه-م1 12 күн бұрын
I did not understand if it is aromatic or not
@VictortheOrganicChemistryTutor 12 күн бұрын
It is.
@الواثقةباللَّه-م1 12 күн бұрын
@VictortheOrganicChemistryTutor Thanks, I do not understand English well, I am an Arab
@triple_gem_shining 12 күн бұрын
These mechanisms are pleasant. I enjoy them
@VictortheOrganicChemistryTutor 12 күн бұрын
I do tend to like carbonyl chemistry and those mechanisms myself too.
@prathameshrumde3027 12 күн бұрын
Awesome
@VictortheOrganicChemistryTutor 12 күн бұрын
Yes, you’re awesome, I agree! 😜
@שםחסום-כ1מ 13 күн бұрын
thank you very much! this practice gave me a dipper and better understanding of H-NMR
@VictortheOrganicChemistryTutor 12 күн бұрын
You’re very welcome! Spectroscopy is one big puzzle, the more you do it, the better you become.
@subhekchasharma2537 14 күн бұрын
Please tell me how many 1)structural 2)gi 3)optical 4)stereo 5)total isomers exist for the monocholoination pdt of methyl cylohexane the numbers 🙏🙏🙏🙏🙏
@jefrysax 15 күн бұрын
i have a question for the 22.10 min reacton. If we have a ketone where the R - are to benzene rings, can we still produce a nitrille as a product or the aromatic rings make it difficult?
@VictortheOrganicChemistryTutor 15 күн бұрын
Formation of a cyanohydrin is an equilibrium and in the case of benzophenone you will have hard time pushing it towards the product but yes, overall it’s quite possible.
@asjednazir6582 15 күн бұрын
Wasted 10 min of my life
@VictortheOrganicChemistryTutor 15 күн бұрын
Nice 😊 thanks to your comment, my engagement rate went up, so even more people will see this video now. Keep hating 👍
@adeolatosinbenjamin8569 16 күн бұрын
Thank you so much for this wonderful video.....From Washington D.C. (USA)
@VictortheOrganicChemistryTutor 15 күн бұрын
I'm glad you found it helpful! 😊