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these videos are saving my life! does anyone else love the "firework-esque" look of the colors he uses on the black background? haha :P
Thank you! You're such a great teacher. It is so commendable what you're doing for students like myself!
You are making me understand my Organic Chem 1 class. I feel like sending you money
Thank you!!I feel smarter after every video XD
THANK YOU, I never understood where that Newman Projection drawing stands for!
To clarify, the methyl groups behind each other is called fully eclipsed and the methyl groups behind a hydrogen is called eclipsed.
imma top organic chemistry!
You should explain stability and potential energy with regards to angular strain, torsional strain, and stearic hindrance.
where have you been all my life/??? love your videos!! they are soo helpful!!! thank you!!!!!!!!
Thank you for saving my life! *virtual hug*
I hope him to arrange a specific playlist for Inorganic Chemistry in his channel...
Great lesson on this topic! 😊
when doing a conformational analysis, to get the conformations in correct order, would you rotate each time the back carbon by 60 degrees starting with the anti? Or would you rotate 120 to get gauche and then 60 to get eclipsed?
I love you, Khan Academy!
Thanks a lot! Very helpful!!!
Thanks many.
You are a god among men!
beautiful explanation...☺
I'm watching this whole O-Chem playlist before taking it in January :)
What about an eclipsed conformation where the methyl groups are behind a hydrogen? Does that conformation have its own special name?
Does it matter whether you rotate the back or front carbon?
In which playlist are this videos on organic chemistry on? I've searched your channel but I can't seem to find them...
Sal for president
what is the difference between staggered conformation and anti-conformation?
thank you!
Awesome!
What if the methyl group has a DA of 60 degrees, will it be more stable than the Gauche comformation?😮 Thanks a lot
very nice explanation.
@kitina11454 Anti-conformation IS a staggered conformation. Staggard is the opposite of eclipsed.
You are the man.
what if the methl group was rotated to sit behind the hydrogen? is that a thing or not?
***** i now know that after a semester of ochem lol thank you though
Eric M "LOL"
thanks!!!!
i bet he is good at counter strike, cause its hard to write nice
Nerdy valentines: "How I feel for you is commonly represented in popular culture by a symbol very similar to a Newman projection of a CH3• radical."
You are my hero
what if the back Carbon CH3 stands behind the H of front one ?Does it has any name ? What about the its potential energy ?By the way THANKS ALOT
What if the back methyl group had a DA of 120 degrees? Would it be more or less stable than 60 degrees?
+Cory Hansen more stable than 60 degrees as CH3 compounds have less repulsion between them and hence stay more stable than 60 degrees
amazinGGGGG!!! :D
Same.....but mines is in 2 days...
Can't we write the 3rd branch as directly ch3
Adarsh Srivastava yes
I don't believe it does, just as long as you only rotate one
where's part 3!?
keşke altyazı olsa
I love you
#15
Nerdy valentines.
Usually your videos help me understand concepts but this video didn't help me understand Newman Projections.
Please somebody help me
bulane
A lot of people recommend Khan Academy for help, not to be mean but this video didn't really help me. : /
can you just replace my prof? Please!!!
these videos are saving my life! does anyone else love the "firework-esque" look of the colors he uses on the black background? haha :P
Thank you! You're such a great teacher. It is so commendable what you're doing for students like myself!
You are making me understand my Organic Chem 1 class. I feel like sending you money
Thank you!!
I feel smarter after every video XD
THANK YOU, I never understood where that Newman Projection drawing stands for!
To clarify, the methyl groups behind each other is called fully eclipsed and the methyl groups behind a hydrogen is called eclipsed.
imma top organic chemistry!
You should explain stability and potential energy with regards to angular strain, torsional strain, and stearic hindrance.
where have you been all my life/??? love your videos!! they are soo helpful!!! thank you!!!!!!!!
Thank you for saving my life! *virtual hug*
I hope him to arrange a specific playlist for Inorganic Chemistry in his channel...
Great lesson on this topic! 😊
when doing a conformational analysis, to get the conformations in correct order, would you rotate each time the back carbon by 60 degrees starting with the anti? Or would you rotate 120 to get gauche and then 60 to get eclipsed?
I love you, Khan Academy!
Thanks a lot! Very helpful!!!
Thanks many.
You are a god among men!
beautiful explanation...☺
I'm watching this whole O-Chem playlist before taking it in January :)
What about an eclipsed conformation where the methyl groups are behind a hydrogen? Does that conformation have its own special name?
Does it matter whether you rotate the back or front carbon?
In which playlist are this videos on organic chemistry on? I've searched your channel but I can't seem to find them...
Sal for president
what is the difference between staggered conformation and anti-conformation?
thank you!
Awesome!
What if the methyl group has a DA of 60 degrees, will it be more stable than the Gauche comformation?😮 Thanks a lot
very nice explanation.
@kitina11454 Anti-conformation IS a staggered conformation. Staggard is the opposite of eclipsed.
You are the man.
what if the methl group was rotated to sit behind the hydrogen? is that a thing or not?
***** i now know that after a semester of ochem lol thank you though
Eric M "LOL"
thanks!!!!
i bet he is good at counter strike, cause its hard to write nice
Nerdy valentines: "How I feel for you is commonly represented in popular culture by a symbol very similar to a Newman projection of a CH3• radical."
You are my hero
what if the back Carbon CH3 stands behind the H of front one ?Does it has any name ? What about the its potential energy ?By the way THANKS ALOT
What if the back methyl group had a DA of 120 degrees? Would it be more or less stable than 60 degrees?
+Cory Hansen more stable than 60 degrees as CH3 compounds have less repulsion between them and hence stay more stable than 60 degrees
amazinGGGGG!!! :D
Same.....but mines is in 2 days...
Can't we write the 3rd branch as directly ch3
Adarsh Srivastava yes
I don't believe it does, just as long as you only rotate one
where's part 3!?
keşke altyazı olsa
I love you
#15
Nerdy valentines.
Usually your videos help me understand concepts but this video didn't help me understand Newman Projections.
Please somebody help me
bulane
A lot of people recommend Khan Academy for help, not to be mean but this video didn't really help me. : /
can you just replace my prof? Please!!!
Thanks a lot! Very helpful!!!