SOO helpful, finally got this information to click. The ethane one made sense, but I was struggling forever on what happens when more carbons are involved!
I believe your energy diagram is off. Eclipsed conformations are supposed to have higher energy, and staggered conformations are supposed to have lower energy. A staggered conformation with 180 degrees is most stable and should have the lowest energy while an eclipsed conformation of 0 and 360 degrees should have higher energy levels and be least stable. Correct me if I'm wrong, that's the way I learned it this semester.
Surely which angle corresponds to the highest energy is arbitrary (based on the choice of 0 degree datum)? You and Leah don't disagree on the fundamental point (i.e. that the staggered conformations have lowest energy).
I think we're actually on the same page here. My use of angles does not refer to the separation of groups, Instead I use the degrees to show how much I rotate. Starting with any arbitrary structure, turn 60 degrees at a time to keep alternating between staggered an eclipsed. the degree value is a measure of how much I've turned my starting molecule
Thank you so much, I hope and wish you will keep uploading more ochem and biology playlist! You are awesome at explaining, teaching and helping students understand what they need to know. thank you so much, and (i have three youtube accounts and i have all three youtube subscribed to you :) thank you and please keep uploading! :)
You are awesome, I'm taking this course in the summer as a prep for the MCAT, did not understand it at all until I watched your videos. Thank you so much!!!
It does not matter in which direction you rotate. However, in this video, I chose to rotate the substituents on the backmost carbon of the Newman projection in the clockwise direction.
Explained 100x better than my textbook did. Thank you so much. Your videos have been so helpful, I am so grateful Leah!
You're very welcome, I'm so glad it helped clear things up!
This explanation was perfect! I Finally understand it better!
I'm glad it helped!
Awesome explanation!
Thank you for your time and effort! So far your are helping with my test for tomorrow!!
Keep up the good-hear-ted tutoring work!
my exam too xD
So happy I was able to help!
SOO helpful, finally got this information to click. The ethane one made sense, but I was struggling forever on what happens when more carbons are involved!
I'm so glad I could help you make sense of it!
Thank you so much! I finally understand this concept :D
You're very welcome!
Your amazing. Wow. Thank god for people like you.
Thank you for your kind words
I believe your energy diagram is off. Eclipsed conformations are supposed to have higher energy, and staggered conformations are supposed to have lower energy. A staggered conformation with 180 degrees is most stable and should have the lowest energy while an eclipsed conformation of 0 and 360 degrees should have higher energy levels and be least stable. Correct me if I'm wrong, that's the way I learned it this semester.
Surely which angle corresponds to the highest energy is arbitrary (based on the choice of 0 degree datum)? You and Leah don't disagree on the fundamental point (i.e. that the staggered conformations have lowest energy).
I think we're actually on the same page here. My use of angles does not refer to the separation of groups, Instead I use the degrees to show how much I rotate. Starting with any arbitrary structure, turn 60 degrees at a time to keep alternating between staggered an eclipsed. the degree value is a measure of how much I've turned my starting molecule
you've saved my life.. Ochem midterm tomorrow... :I I really couldn't understand my professor or the text.
P.S. you're an awesome teacher.
So happy I was able to help you!
Thank you so much, I hope and wish you will keep uploading more ochem and biology playlist! You are awesome at explaining, teaching and helping students understand what they need to know. thank you so much, and (i have three youtube accounts and i have all three youtube subscribed to you :) thank you and please keep uploading! :)
I'm so happy I could help and thanks so much for your subscription!
Your videos are so helpful! Thank you :)
you're very welcome
This video was really much helpful .
I'm so glad it helped!
You're the best !! Thank you for the great explanation :)
You're so very welcome!
This clearly explained each step. For new one
Thanks ❤️
you're so welcome
Excellent explanation madam you've really helped me..... Thank you so much
You're very welcome!
Thank you mam , for this video!!!!
You're welcome :)
thank you sooooo much for this video !! finally i understand it !
Glad the video helped you understand the topic better! You're welcome!
thank you!! this helps a lot
You're so welcome, very happy to help!
You are awesome, I'm taking this course in the summer as a prep for the MCAT, did not understand it at all until I watched your videos. Thank you so much!!!
you're so welcome, happy to help!
Just amazing) I was very handu☺️ BIG LIKE
Thank you!
another helpful explanation. tyvm!
You're very welcome!
thank you so much :) now i have better understanding about this topic
You're welcome! Glad I could help!
Thank you again; you are the Angel Teacher ;)
You're very welcome, glad you liked it!
you are amazing ! i only watch your videos
Thanks so much!
Thank you it is very useful to understand
You're welcome! I'm happy to help clear it up for you!
very clear thanks
you're welcome!
Thanks good explanation 👍🏻👍🏻👍🏻
Glad it was helpful!
You are amazing thank you
You are very welcome!
Thank you ma'am 🤩
You're welcome 😊
Very helpful thank you
You're so welcome!
is the rotation clockwise or counter clockwise?
It does not matter in which direction you rotate. However, in this video, I chose to rotate the substituents on the backmost carbon of the Newman projection in the clockwise direction.
good explanation
thanks
thank you!
you're welcome!
thankyou😊😊
You're welcome!
Thank you alot
You're very welcome!
THANK YOU!
You're very welcome!
Dr fantastic
Glad you liked it
Thanking you
You're welcome
Thnx u so much
You're very welcome!
Thanks alot
You're welcome!
From Algeria ❤ thanks
you're welcome
Helpful
Glad to hear that!
How can I know the postion of 60 degree
I'm sorry, but I don't offer tutoring through TH-cam comments. For more help with this, I recommend joining the orgo study hall: leah4sci.com/join
thanks..
You're welcome
awesome........
Thank you, glad you liked it!
thaaaaaanksssss i have an exam tomorrow :p
You're welcome!
So you got a bad grade I assume.
Privately i apreciate u my prof
Thank you!
Thank you so much! My dumbass friend was disagreeing with him and I rekt him with this video.
You're welcome! Glad to help :)
thanksss so much
You are very welcome!
This is reversed. Anti 180 is lowest energy/most stable confirmation. 0 total eclipsed has the highest energy and is therefore the most instable.
correct! did I misspeak?
👍👍
:)
it is good, but you are going to fast with alots of information :s
It can feel fast for sure! Use the settings to change my speed to whatever works best for you.
Really helpful, thank you very much!
You're very welcome!
Thank you!
you are welcome