Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams & PDF Worksheets: www.patreon.com/MathScienceTutor/collections Access The Full 1 Hour Video on Patreon: bit.ly/3juOc8X SN1 SN2 E1 E2 - 4 Hour Test Review: bit.ly/3Bt4ghw
Speaking on behalf of all Natural Science students from the University of Zambia, your videos have been of great help to us. They've helped us understand most things that lectures couldn't thank you we appreciate you man 👍
Thank you so much. I've used all of your IUPAC, stereochemistry, IR, NMR, and substitution/elimination videos to be able to pass my org chem 1 class. I seriously couldn't have done it without you. You're the best.
I love you and you're amazing.... I'm in my final year now...and your videos has been helping me since my first year... you've been a blessing to millions of people around the world and I hope you know that.
I am a CS undergrad and I don't have ochem(obviously). but, I did learned all these stuff while preparing for 12th standards board exams. Although I would never need these stuff, still watching cause its the organic chemistry tutor.
I'm in class 11 (India)and just tested positive for covid today, but my state isn't conducting online classes hence I need to skip classes for atleast a week. Thank you so much for these videos!
This is the first video of yours I’m watching, but I like how you say one ion “attacks” another one, it’s entertaining to think about atoms battling it out haha
no you're right, he made a mistake. As you go to the right in a row of the periodic table nucleophilicity decreases, for the same reason basicity decreases: the atoms are more stable with their negative charge, leading to them reacting less.
a little late sorry but the iodine has a negative charge while the bromine does not, halogens will be nucleophilic if they are charged but they will be electrophilic if they are attached to a sp3 hybridized carbon
You wanna look at the carbon that attaches to the Bromine atom. Along with the bond to Bromine, it also bonds to two other Carbon atoms. The number of carbon atoms that a carbon is attached to is what determines whether it is primary, secondary, tertiary, etc.
The way that my professor is trying so hard to get everything in while forgetting the fundamental element of teaching that's helpful is deconstruction. Repetition helps a lot but my god is it anoying to take upper level classes and still teach yourself from the textbook.
Well good for you. I learned this in my 3rd year of university here in America. More than half the class was not doing so well and the professor had a hard time explaining concepts effectively. The textbook we had was full of errors and we stopped using it. This was back in 2006 before TH-cam had videos like this explaining concepts clearly.
We learnt in in class 11 here in India ( there’s class 12th then collage ) our teacher is one of the top teachers of India and I use these vids to revise theory before class and exams
Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html
Full-Length Exams & PDF Worksheets: www.patreon.com/MathScienceTutor/collections
Access The Full 1 Hour Video on Patreon: bit.ly/3juOc8X
SN1 SN2 E1 E2 - 4 Hour Test Review: bit.ly/3Bt4ghw
Speaking on behalf of all Natural Science students from the University of Zambia, your videos have been of great help to us. They've helped us understand most things that lectures couldn't thank you we appreciate you man 👍
Fellow uni student in Zambia here, I agree, his content is very helpful.
Education in Zambia exists??🤔
@@calebwilliamson5797bro how you white And in zambia
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15:39 CORRECTION: Nucleophilicity decreases as going from left to the right across the periodic table.
yeee i went straight to the comments after seeing that
@@tdelliott-diab3860 sameee
Ahhhh yeah that makes sense. Cause he wasn't making sense there LOL
Bro i started tweaking out
Thank god for this comment i was tweaking
Thank you so much. I've used all of your IUPAC, stereochemistry, IR, NMR, and substitution/elimination videos to be able to pass my org chem 1 class. I seriously couldn't have done it without you. You're the best.
I’m an industrial Chemistry student from Nigeria. And I just wanna say a big thank you! You’re absolutely the best!
Wot is industrial chem btw
I love you and you're amazing.... I'm in my final year now...and your videos has been helping me since my first year... you've been a blessing to millions of people around the world and I hope you know that.
I'm medical student from libya
You are a great man I don't know what we could do without you💜
why are you learning about sn2 reaction in med school?
I am a CS undergrad and I don't have ochem(obviously). but, I did learned all these stuff while preparing for 12th standards board exams. Although I would never need these stuff, still watching cause its the organic chemistry tutor.
konsa college bro
The funny thing is that right now I'm in chemistry class and this is what the lecturer is teaching....
Perfect timing! 😂
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*perfectly balanced,as all things should be.*
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I'm in class 11 (India)and just tested positive for covid today, but my state isn't conducting online classes hence I need to skip classes for atleast a week. Thank you so much for these videos!
get well soon
Dude American students seem so much dumber that the rest of the world.
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thank you for saving my life from falling apart. I love you
What a co-incident I was Binge-Watching your videos and you upload it now...
Right as I got out of organic lecture this was posted, ty!
This is the first video of yours I’m watching, but I like how you say one ion “attacks” another one, it’s entertaining to think about atoms battling it out haha
I love how you sound like you're having fun teaching these.
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I'm not going to attend my chemistry class anymore,you teach more accurate than my lecture
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At 15:39, did you mean nucleophilic strength decreases as it goes to the right?
Yes he did
I also don't get it clear
@@marcandmusicc I think it should decrease
I think bascisity increases across the row which means a stronger nucleophile
@@Sheldon_J.Plankton no. Nucleophilicity decrease as going from left to the right on periodic table
Pre med students from around the world thank you
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Thank you for the videos!! I am using them as practice for my ochem2 final
howd it go?
15:21 The solvent matters a lot. H2O is a protic solvent and doesn't favour SN2 reactions. Aprotic solvent favours SN2 reactions.
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10:44 benzene variations
20:39 H2O, deprotonation
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W in the chat. Bro I now understand better. Big Up
So protic solvents aren't good at all for fluorine, right? Stabilizing it is the last thing you want
so the nucleophilic strength decreases to the right? or increases to the right?
nucleophilic strength decreases to the right, he made a mistake
I’m about to take an advanced organics class for grad school and I’m terrified.
Just commenting for the algorithm. {pls. comment so he can get more views}
Thank you for saving many asses getting whooped over all these years
15:34 seems backwards, but I suppose the electronegativity will depend upon the solvent/solution
no you're right, he made a mistake. As you go to the right in a row of the periodic table nucleophilicity decreases, for the same reason basicity decreases: the atoms are more stable with their negative charge, leading to them reacting less.
@@tdelliott-diab3860 so, F- have stronger nucleophilicity than OH- and the weakest is NH2-?
how can H2O a weak nucleophile/weak base react with a primary alkyl halide that can’t undergo rearrangements in SN2??
THANK U SO MUCH
Is NaBr not formed as well at 2:34 ?
Super well explained
15:34 is confusing....... 🙄
Why would iodine, in potassium iodide, displace bromine when bromine is more nucleophilic than iodine? Thanks.
a little late sorry but the iodine has a negative charge while the bromine does not, halogens will be nucleophilic if they are charged but they will be electrophilic if they are attached to a sp3 hybridized carbon
at 10.27 how is the structure on the left a secondary structure
You wanna look at the carbon that attaches to the Bromine atom. Along with the bond to Bromine, it also bonds to two other Carbon atoms. The number of carbon atoms that a carbon is attached to is what determines whether it is primary, secondary, tertiary, etc.
At 1:23 isn't the bromine supposed to pull away
Good
I love you
The way that my professor is trying so hard to get everything in while forgetting the fundamental element of teaching that's helpful is deconstruction. Repetition helps a lot but my god is it anoying to take upper level classes and still teach yourself from the textbook.
now heres a question for you
15:47
commenting for the algorithm
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🙋♂️ hi
What's your name or instagram ID?
He can teach literally any subjects except organic chemistry XD
How r yall learning this in college...im learning this in high school 💀💀
We also learnt the same when we were in high school but in tertiary they add more detail..more flesh
Well good for you. I learned this in my 3rd year of university here in America. More than half the class was not doing so well and the professor had a hard time explaining concepts effectively. The textbook we had was full of errors and we stopped using it. This was back in 2006 before TH-cam had videos like this explaining concepts clearly.
We learnt in in class 11 here in India ( there’s class 12th then collage ) our teacher is one of the top teachers of India and I use these vids to revise theory before class and exams
You are a beautiful beautiful man, many thanks
600th viewer
a lot of this is wrong
really??
@@yasmin90snah he is lying