I was confused about when these shifts occurred, even after reading the textbook. Thanks for clearing this up for me! Clear, concise, and great visuals!
Thank! I was lazy in my senior high days and college professors require you to know everything you've learned in high school. These videos are really helpful!
thank you so much miss Melissa you are a life saver I missed all the organic chemistry lessons with my chem teacher for some reason, however after watching your videos I feel so relieved
I'm a visual learner so listening to my professor explain this was confusing. Your videos really help. If you can talk about Sn 1 and Sn2 mechanisms as well that would be awesome. Thank you !
@@amiinaden4132 but different people do have different learning preferences don't they? learning style is also just a simple way to state your preference
I really really like ur video so much madam...plz keep on doing... Ur thinking and ur words are so positive ... I feel happy..ur way of teaching is so good it's colourful ...cool.. I like it .it's easy to learn .u helped me a lot.. thank you . Plz upload more videos...
At 1:52 hydride-shift can occur but it makes a minor product. The major one, a six membered ring, is produced by ring expansion in the reaction. Anyone let me know if I am wrong.
I have one doubt that if one tertiary carbocation is present next to another tertiary carbon and if shifting would take place the carbocation on next carbon would be more stable (on the basis of hyperconjugation)........ So shifting would take place or not??
Does anyone know how to download the chem guides? Tried both organic and general chem and all it does is open a webpage and show the graphic of the study guides. I figured something was supposed to automatically download since there's no buttons, but it doesn't seem to do anything. Tried both chrome and avast browsers and nada. If anyone knows how to download them, shoot me a reply if you want. Much appreciated.
Did you enter your email when you opened the webpage? If so, then you will get an email with a link to download the guide. Sometimes it goes to your spam/junk folder.
Oh I see what you mean. There's a name and email address bar that doesn't show up on my browser, only my phone. Thanks for the help and keep making videos! They're awesome and just between us, you're a much better teacher than most chem professors or TH-camrs, but don't tell them I said that. Cheers and hope you have a lovely Christmas (if you celebrate it, if not have a good next Wednesday).
Amazingly helpful video as always. I have another question that's not related to this video, so I apologize for that, but I was wondering if it's true that you can find the valence electron of a transition metal by their electron configuration. We have a test tomorrow in my Chemistry class and we've been learning about ionic and covalent compounds as well as polyatomic ions and my teacher didn't really tell us how to find the valence electrons of a transition metal that much so... I kinda searched it up and I wasn't sure so I wanted to ask you before I even think of applying that to the test. ☺️💕
Hi Selena, yes this is true, you add the electrons that are in the highest energy shells (the highest coefficient). For example for Carbon, it has an electron configuration of 1s2 2s2 2p2, we only add the electrons in the highest energy shells so that would be 2sp2 and 2p2, 2+2 gives us 4 valence electrons which is correct for carbon.
Ngl I actually like organic better than gen chem because there’s no math. I think it’s overhyped how hard organic is. You just gotta get used to the spatial thinking; it feels weird after just being able to use formulas and plug things in for gen chem, but you will get used to it. Just know the basic rules of what part of the molecule is the most reactive and that will make thorns much easier!
Watch me guide a student through Organic Chemistry in my new Study With Us series:
th-cam.com/play/PLytGGifnD9dVDyYJjpRuefMehMvIn15JY.html
Are u an Indian ?
I was confused about when these shifts occurred, even after reading the textbook. Thanks for clearing this up for me! Clear, concise, and great visuals!
Thank! I was lazy in my senior high days and college professors require you to know everything you've learned in high school. These videos are really helpful!
This is the best video on carbocation rearrangement! Thank you!
The amount of efforts you put to make these videos is commendable..💫
In the app the example shown @3:00 , they call the shift an alkyl shift, is this another way of saying methyl shift?
Methyl is alkyl group so its basically same
The construction of the video i just loved it
I was having trouble remembering when to use which rearrangement and this video was super helpful, thank you !
Thanku for making this vedio ma'am it's really very helpful to me..... Lots of love and respect from India
Love from India mam, I finally understood it
thank you so much miss Melissa you are a life saver I missed all the organic chemistry lessons with my chem teacher for some reason, however after watching your videos I feel so relieved
The video production is just amazing, thank you so much.
I'm a visual learner so listening to my professor explain this was confusing. Your videos really help. If you can talk about Sn 1 and Sn2 mechanisms as well that would be awesome. Thank you !
The style of learning is a myth
@@amiinaden4132 but different people do have different learning preferences don't they? learning style is also just a simple way to state your preference
Thank you mam for such a good explanation 🧡
Finally I understood this concept thanks ma'am ur doing a marvelous job ...
Now I feel more confident for my org exam tomorrow, thank you Melissa!!
Thanks!! Your visuals help so much!
Aww thank you so much!! 😊
T
That was an awesome class....simple and perfect!!!
Came from your tiktok I’m ready to pass this next semester
Love it!
A doubt: what about ring expansion in the cyclopentane molecule? Does a 3° carbocation bring more stability than expanding the ring?
That’s what I thought too.
Yes
But here she taught about hydride shift how it happen ... Nice video
I found you from TikTok and I’m so grateful! You have helped me so much with chemistry this semester! Thank you so much ❤️
Yay!! You are so welcome 😊
I really really like ur video so much madam...plz keep on doing... Ur thinking and ur words are so positive ... I feel happy..ur way of teaching is so good it's colourful ...cool.. I like it .it's easy to learn .u helped me a lot.. thank you . Plz upload more videos...
Thanks a lot....mam 💘 love from India 🇮🇳u make me soo happy..as u cleared my all doubts.....
At 1:52 hydride-shift can occur but it makes a minor product. The major one, a six membered ring, is produced by ring expansion in the reaction.
Anyone let me know if I am wrong.
Thanks a lot! A lot better❤
Ooo waaoooo it's too much great way to get understand....
Thanking you always 😎😍😍😘
Like your lactur.....
Really awesome 😎😎
Hi there!! It was just awesome... You explained it very well☺️
Thanks!!
Your channel is so helpful! I hope you upload more organic chemistry 2 videos. Alcohol rxns are super confusing!
Thank you so much you helped me so much.❤🌹
THANK YOU
Thank you so much, this was soo helpful!!
For methyl shifts to happen, do the carbon with the + and the methyl-donating carbon need to be adjacent?
Thanq so much mam
I have one doubt that if one tertiary carbocation is present next to another tertiary carbon and if shifting would take place the carbocation on next carbon would be more stable (on the basis of hyperconjugation)........ So shifting would take place or not??
thank you for this video
In cyclopentane example why is not ring expansion first and then hydride shift ?
How if the double bond next to only 2 different carbon? Is it alkyl or hydride?
Whenever I see her video I always wonder how much she have to cut and paste everything!
Does anyone know how to download the chem guides? Tried both organic and general chem and all it does is open a webpage and show the graphic of the study guides. I figured something was supposed to automatically download since there's no buttons, but it doesn't seem to do anything. Tried both chrome and avast browsers and nada. If anyone knows how to download them, shoot me a reply if you want. Much appreciated.
Did you enter your email when you opened the webpage? If so, then you will get an email with a link to download the guide. Sometimes it goes to your spam/junk folder.
@@melissamaribel Wow quick reply. Big thank you already. By enter my email, do you mean login?
Oh I see what you mean. There's a name and email address bar that doesn't show up on my browser, only my phone. Thanks for the help and keep making videos! They're awesome and just between us, you're a much better teacher than most chem professors or TH-camrs, but don't tell them I said that. Cheers and hope you have a lovely Christmas (if you celebrate it, if not have a good next Wednesday).
Strange I didn’t know that was happening, thanks for letting me know. And thank you so much 😊 Hope you have a wonderful Christmas too 🎄
Mam u r great ...
What can I do if I haven’t received the stud guide
Thanks for emailing me Jenny, glad I was able to get it to you. 😃
Thank you so much !!! I’m just stressed that I can’t even email correctly.
Won't there be ring expansion?
I like this, but use less confusing examples for those who may be completely lost. It just makes it harder to understand
Amazingly helpful video as always. I have another question that's not related to this video, so I apologize for that, but I was wondering if it's true that you can find the valence electron of a transition metal by their electron configuration. We have a test tomorrow in my Chemistry class and we've been learning about ionic and covalent compounds as well as polyatomic ions and my teacher didn't really tell us how to find the valence electrons of a transition metal that much so... I kinda searched it up and I wasn't sure so I wanted to ask you before I even think of applying that to the test. ☺️💕
Hi Selena, yes this is true, you add the electrons that are in the highest energy shells (the highest coefficient). For example for Carbon, it has an electron configuration of 1s2 2s2 2p2, we only add the electrons in the highest energy shells so that would be 2sp2 and 2p2, 2+2 gives us 4 valence electrons which is correct for carbon.
@@melissamaribel Thank you so much! This really helped and now I'm pretty confident for the test tomorrow :) ♡♡♡
Please make more☹️ more about like aromatic compound benzene☹️ I looooove your videos
Assulaikum mam Mai Pakistan sai ho mujhy organic chemistry Kai notes. Chaiyay thy but download nahi ho Rahe
Please we need more organic chemistry videos resonance fisher
Understood!!
You beautiful beautiful goddess; I have an exam tomorrow thank you so much!!!
When are you going to make more Organic Chemistry videos and make flashcards???
Ngl I actually like organic better than gen chem because there’s no math. I think it’s overhyped how hard organic is. You just gotta get used to the spatial thinking; it feels weird after just being able to use formulas and plug things in for gen chem, but you will get used to it. Just know the basic rules of what part of the molecule is the most reactive and that will make thorns much easier!
Things*
❤
👍
Pls gove more examples.. Explain un detail.. Then only it would be beneficial