Thanks so much! I'm taking Organic 1 and 2 online. I've been watching my professors vodcasts and re-reading my text for TWO WEEKS and had no idea what the difference between Sn2, Sn2, E2, and E1 were until your videos! These videos are a LIFE SAVER! (or grade saver for the less melodramatic students) Thanks again!
+Bob Hanks Thanks Bob! No "lin" though...just Frank! haha I'm happy to hear that my vid could help though! Here are some extra resources in case you need to find something not on my channel: orgomadeeasy.org/extra-resources/
Oh man that sounds like a tough one, thanks for the positive feedback though. Hope it went alright! Just a note for the future: A good way to study is to teach/explain these problems and concepts to your friends too to make sure you really/actually understand it. :]
Jacqueline Ollison I just wanted to let you know that I recently finalized my Patreon page. So if you're interested in either getting more reliable updates from me for new videos or helping support the creation of these videos, you can check out my new Patreon page: @OrgoMadeEasy (I have a Free Tutoring Lottery set up there that you might be interested in. :D)
Haha thanks Karine! I actually just figured it out when I was planning this video. And the sound effects I'm afraid I have to give credit to Prof. Rubio of BU who's absolutely hilarious.
In the textbook I'm using, it says that we need to draw newman projections to determine if the way the bonds around the C-C double bond are cis or trans: the co-planar and anti-co-planar concept. Could you possibly explain that or better yet make a video if you have time :)? Thanks
whadduprich Ah good point! So not all nucleophiles are good bases for example I- or -SH or Br-. I- and Br- are both conjugate bases of very strong acids so they are highly unlikely to act as a base. And usually bigger atoms like sulfur don't make good bases. Now the Tert-butoxide and T-butanol molecules that I use in my videos are not so great nucleophiles do to them being chunky and bulky. Elimination occurs mostly when the conditions for substitution aren't so great. E2 for example occurs if you have a leaving group on a tertiary carbon. There's absolutely no chance of SN2 and your strong nucleophile that can act as a base will not wait a long time for the leaving group to leave and for a carbocation to form, in order to do an SN1. It's just going to go straight ahead and do a E2.
Thanks so much! I'm taking Organic 1 and 2 online. I've been watching my professors vodcasts and re-reading my text for TWO WEEKS and had no idea what the difference between Sn2, Sn2, E2, and E1 were until your videos! These videos are a LIFE SAVER! (or grade saver for the less melodramatic students)
Thanks again!
Alexandria Pankoke Haha that's hilarious! No problem at all, it's so awesome to hear that. Thanks for the feedback. #MissionAccomplished ;)
I love your videos! As someone who struggles with orgo, you've helped so much!! Thank you!!
@@samoyedand2huskies thank ya for watching! 😄
@@samoyedand2huskies where are ya taking Organic Chem at? 🙂
@@OrgoMadeEasy Im taking it at University of North Carolina in Charlotte! ☺
that was a smooth analogy on the backpacks for steric hinderance.
👍🏼😊 - Analogies FTW!
Thanks Franklin, your video covered an important part of my exam. Very helpfull!
+Bob Hanks Thanks Bob! No "lin" though...just Frank! haha I'm happy to hear that my vid could help though! Here are some extra resources in case you need to find something not on my channel: orgomadeeasy.org/extra-resources/
Thanks Frank!!
Oh man that sounds like a tough one, thanks for the positive feedback though. Hope it went alright! Just a note for the future: A good way to study is to teach/explain these problems and concepts to your friends too to make sure you really/actually understand it. :]
WHY ARE YOU SO GREAT!!!
Jacqueline Ollison Because you guys are awesome and deserve it!!!! :D
Jacqueline Ollison I just wanted to let you know that I recently finalized my Patreon page. So if you're interested in either getting more reliable updates from me for new videos or helping support the creation of these videos, you can check out my new Patreon page: @OrgoMadeEasy (I have a Free Tutoring Lottery set up there that you might be interested in. :D)
I wish my professors teach like you
Haha thanks Icedookie, you can try coming up with some analogies and stories yourself for some of the Orgo concepts ;).
Haha thanks Karine! I actually just figured it out when I was planning this video. And the sound effects I'm afraid I have to give credit to Prof. Rubio of BU who's absolutely hilarious.
Love the "anti" hydrogen explanation on top methyl group. ..esp sound effects;)
thank you chang chi
Haha now you'll never forget the spinning methyl hydrogens :D
Good work, thanks 🙏
Sir I know it is easy question but I don't understand better that's why I'm asking you how we check stability of compound I want answers in vedio plz.
Thanks Nate!
wait how did you know which hydrogens are dashed and wedged?
Awesome Explanation.
the part one link sent me right back here. im assuming this is the part 1 you were referring to lol
In the textbook I'm using, it says that we need to draw newman projections to determine if the way the bonds around the C-C double bond are cis or trans: the co-planar and anti-co-planar concept. Could you possibly explain that or better yet make a video if you have time :)? Thanks
What molecule kit is that?
good work
can 1 degree aromatic alcohol undergo S1 OR E1 Reaction mech i want some examples
Please help!!!!
Thank you:)
im so confused i thought Nu- (nucelophiles) are bases.....
whadduprich Ah good point! So not all nucleophiles are good bases for example I- or -SH or Br-. I- and Br- are both conjugate bases of very strong acids so they are highly unlikely to act as a base. And usually bigger atoms like sulfur don't make good bases. Now the Tert-butoxide and T-butanol molecules that I use in my videos are not so great nucleophiles do to them being chunky and bulky. Elimination occurs mostly when the conditions for substitution aren't so great. E2 for example occurs if you have a leaving group on a tertiary carbon. There's absolutely no chance of SN2 and your strong nucleophile that can act as a base will not wait a long time for the leaving group to leave and for a carbocation to form, in order to do an SN1. It's just going to go straight ahead and do a E2.
I love you
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Wangbadaang
Why isn't that beta hydrogen it's close
Which one are you referring to? The ones on the CH3 methyl group of the Beta Carbon on the left?
Hmm no that's weird lol I just tested the link, it should be to this video: th-cam.com/video/gGt6T-BVDsU/w-d-xo.html