Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams and Worksheets: www.patreon.com/MathScienceTutor/collections Next Video: kzitem.info/news/bejne/u4OZqap6bpZ1gIo Alkene Reactions: kzitem.info/news/bejne/zYGItYxnfGJ7hag
@Ben-dv8xw
4 жыл бұрын
Thank you for consistently putting out all these videos. I appreciate you going back over the basics like this video. Im going to school to become a highschool chemistry teacher and i plan on using alot of your techniques so thank you again.
@shravjally4896
4 жыл бұрын
Ben Charlton copy car!!
@Shreyas0832
4 жыл бұрын
Thanks a lot buddy 🙏🏻🙏🏻🙏🏻🙏🏻
@NourMuhammed-l7q
Жыл бұрын
amazinggggggggggggggggggggggggggggggggggggggggg
@mahbubaafroz1671
9 ай бұрын
So the hydrogen atoms wanna join the bois
@burntsweetpotato3747
3 жыл бұрын
i feel so dumb... i dont get this
@sc4ramouch3
2 жыл бұрын
me fr
@Ammaryan
2 жыл бұрын
The hydrogen atom is attached to the carbon atom with the larger number of hydrogens while the halogen (negative ion) is attached to the carbon atom with the lower number of hydrogens
@duababar2201
2 жыл бұрын
You are not alone
@Keylisha-c2o
Жыл бұрын
He's explanation is complicated
@abbeyjosephine522
Жыл бұрын
markovnikov’s rule is just saying that the heavier atom will add to the more substituted carbon (a Br will add to a tertiary carbon over a secondary carbon)
@JTurn916
4 жыл бұрын
I’m sad I don’t really watch these vids anymore because I’m done with chemistry for now but thanks for helping me get A’s!
@miracleogbuagu7627
2 жыл бұрын
How to know if it is anti markovnikov
@circlefont
Ай бұрын
If it has a peroxide,, i know im 2 years late 💀
@floga10
3 жыл бұрын
I get why markovnikov addition proceeds because a primary carbonation is unstable, but then what would be favorable about having anti-markovnikov addition and how would we know when those happen instead?
@nickmedina1317
2 жыл бұрын
That’s what I’m trying to figure out
@rudrajoshi1598
2 ай бұрын
I am not an expert but During some reactions ( reactions which follow Anti Markonikov rule) free radicals are formed When we react butane(CH3CH2CH2CH3) with HBr and ROOR Br reacts first and forms a free radical as follows A Transition state is formed CH3CH2CH(Br)CH2• (here • represents free radical) Now the we will stabilise the free radical CH3CH2CH•CH2Br The free radical is more stabilised due to hyper conjugation hence now the H• atom will attack the free radical forming CH3CH2CH2CH2Br or 1 bromo butane Hope this helps 👍🏼
@anuragg7007
4 жыл бұрын
In India it's thought in high school in depth of application to it. Like we literally had 4 chapters linking to it. "Great Video And Awesome Explanation" Love from India🇮🇳😍
@xaej1he144
2 жыл бұрын
Taught*
@arjunt1453
2 жыл бұрын
And that's Indian education system! 🥺
@akarsh_xd
2 жыл бұрын
@@xaej1he144 typo
@Shogun507
7 ай бұрын
*Taught*
@joshuamitchell5530
4 жыл бұрын
Can you do some videos on some more advanced concepts such as rearrangements, maybe some reactions such the Wittig reaction and other carbonyl reactions.
@ayanleahmed1316
Жыл бұрын
Wittig reactions is simple
@joshuamitchell5530
Жыл бұрын
@@ayanleahmed1316 well it depends on your level. This channel has mainly been doing intro organic chemistry vids so the wittig would be quite advanced in comparison. Also explaining the stereochemical outcome isn’t simple.
@ayanleahmed1316
Жыл бұрын
@joshua , add a Carbonyl compound with phosphorane to form alkenes, this is a very simple way to prepare Double bond Hydrocarbons .
@joshuamitchell5530
Жыл бұрын
@@ayanleahmed1316 That’s incorrect. You add a carbonyl compound to a phosphonium ylide not a phosphorane. And would you be able to explain the stereochemical outcome?
@Illic-_-
2 жыл бұрын
7:19 why does this reaction not include a hydride shift? You have explained earlier in the video that the more stable Carbocation is formed which is in this case a secondary carboncation. But now there is a secondary carbocation adjacent to a tertiary carbocation, wouldnt someone expect a hydride shift?
@metastag
2 жыл бұрын
because when you go inside their mechanism, an actual free carbocation is never created, in the case of oxymercuration reaction, a cyclic carbocation is created where no rearrangement is possible, hence the tertiary carbocation is not formed
@philippedukeoforleans6766
4 жыл бұрын
THANKS A LOT SIR :>
@annablueseas
11 ай бұрын
thank you so much. this makes 100% sense now compared to my textbook 👌
@SiscoMontego
4 жыл бұрын
Hey, I've trouble to understand the reaction with on of your example with Hg(OAc)2. What does this Hg-molecule do (in detail)? Do you have a video that already covers this topic?
@fruityliciousk2704
4 жыл бұрын
search for the oxymercuration demercuration video on his channel :)
@fruityliciousk2704
4 жыл бұрын
search for the oxymercuration demercuration video on his channel :)
@兔子和花椰菜
2 жыл бұрын
@@fruityliciousk2704 just wondering, so it is different from react with HBr which has a hydride shift that Br ion attacks tertiary carbocation instead?
@chemistryrajsekhar8012
3 жыл бұрын
Mr tutor .... ur my best after my mother
@JZSPAID
4 жыл бұрын
My orgo 1 final is in 3 days and you upload this.. can you read minds bro?
@arhamapon9282
2 жыл бұрын
I think on 1 minut and 45 seconds of the video, you said," the hydrogen is gonna go to this carbon, the one with the most number of CARBONS" I think you intended Say "hydrogen"
@onebeets
3 жыл бұрын
commenting so more people see this
@SamstarCREates
4 жыл бұрын
Love from India 🇮🇳
@lifeofafangirl2935
2 жыл бұрын
Even if I jump in the cliff rn I really can't understand this lesson. AMEN
@melgerzhon
4 жыл бұрын
Sir, are you a chemist?
@onebeets
3 жыл бұрын
good thing youtube nametags don't exist so we'll never know
@jumausman6985
3 жыл бұрын
thank you sir organic has been hell for me since 11th grade.
@linkth3rd429
Жыл бұрын
Where is the O-H group coming from in your examples?
@saraisteenson7413
4 жыл бұрын
u never disappoint bro
@xlyrics1
7 ай бұрын
I love you man❤
@annasener6429
2 ай бұрын
Where is the double bond in pentane? There has to be one isn't it so? I mean in 1:17 minutes
@ummaysalma8049
3 ай бұрын
You teach well, thank you. But you speak a bit fast.
@anaseshmela8512
6 ай бұрын
5:45 Thank you, But seriously where did you find that OH. I mean that whole fraction has nothing to do with OH bruh.. Am I on the right video?
@gerrypalme489
2 ай бұрын
I love all your videos, and its really awesome, it seems like you have mastered all the known subjects, God Bless you and your family, I want to really understand the concept of how the reaction mechanism works.....
@ChloeCurtis-cc7lp
5 ай бұрын
you said in two different markovnikov reactions that the H would go with the best sub carbon but then you said the H will go with the least sub carbon. Which is it?
@trnasmr5746
2 жыл бұрын
My life savior!!!!
@t.lwillow4581
7 ай бұрын
thank you so much ily!
@Physics_is_life
6 ай бұрын
Great revision, thanks
@hamerlee6033
5 ай бұрын
Only HBr and H3O+ will have addition at tertiary carbon rigy?
@andrewgonzales1359
2 жыл бұрын
Lol, does anyone else feel like he’s the Wizard in the Wizard of Oz? Can we see you? Lol
@nololkiez9859
4 жыл бұрын
МАРКОВНИКОВ КРУТОЙ МУЖИК БЫЛ!
@yuvalshah8565
9 ай бұрын
Bruh awsome channel🛐 you won my subscription🤭
@kristynmorales5326
2 жыл бұрын
This is so confusing to me. I don’t understand at all how to know what exactly the molecules with the arrow change the initial molecule to create different products.
@athaleagreenlandindonesia3914
2 жыл бұрын
You should watch his other videos Basically, in a nutshell, Nucleophile attack electrophile
@kagularavindra4886
Жыл бұрын
Nibondha chepavura
@IndigoMist44
10 ай бұрын
nenu koda atlanti confusion lo unnanu. chivariki neeku ardamainda?
@maurice.2496
4 жыл бұрын
🤔
@ShakhawatHossainShovon
3 жыл бұрын
When will you launch an astromy course..?
@mayardalloul8797
4 жыл бұрын
🙏🏻
@mahdimohseni3348
2 жыл бұрын
Thank you
@shahnozamaxmudova3668
2 жыл бұрын
Respect 👍
@oddcon5036
7 ай бұрын
What about pent-3-ene?👀😥
@Musfiqur_anik
Жыл бұрын
I like science stress no problem 👍
@byproslaychannel9753
3 жыл бұрын
thank you
@cecileguignes1534
2 жыл бұрын
So why do you get a 50% 50% of Pent-3-ene and Pent-2ene ? I understood the second one because of Markovnikov's but why 50% for the first compound?
@spcraftsman2656
2 жыл бұрын
If you have an equal chance of getting either of two, in a macro scale, you get 50% of both. It's just probability.
@osaseidahor3428
2 жыл бұрын
I think it’s because the first compound (pent-2-ene) has a double bond where both carbons in the double bond are secondary, so the halogen (Br) has no preference to bond to, for either carbon in the double bond. That’s why the Br bonds 50% of the time to each carbon in the double bond. But for the second compound, but-1-ene, the double bond has a primary carbon and a secondary carbon, so the Br prefers to bond to the secondary carbon, which you understand follows Markovnikov’s rule.
@zh-vu7zc
Жыл бұрын
Excellent Explanation ❤
@tobipurp
5 ай бұрын
Thanks King!
@prabavathiganesan6273
4 жыл бұрын
Hi
@dilru5594
4 жыл бұрын
🤗
@checkmates_only
2 жыл бұрын
All clear bro 👍
@booyah211
Жыл бұрын
Such a helpful video sir!!
@vedhaelumalai9062
4 жыл бұрын
You are really great......I should admit that your voice is awesome... I'm simply addicted....
@panduranganudayakumar8348
3 жыл бұрын
Thank you you videos are very useful
@Kshitij_Punani
8 ай бұрын
Thanklsssss broooooo
@CorneliusMonkeyButtThe3rd
Жыл бұрын
where are all those water molecules coming from LMAO
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