This videos has practice for determining whether a chiral carbon is an R or S configuration. Edit: First example is not chiral. Support us!: / learningsimply Twitter: / learningsimplyv
Thank you, dude!! Your explanation with the H and a wedge has helped so much -- I knew that it needed to be flipped but didn't know how to do it exactly.
Thank u so much, the only video that made me understand R and S, my professor seems to be the only one in the world to do certain exercises with whole molecules, everyone only does the centers, thanks man
Thank you, dude!! Your explanation with the H and a wedge has helped so much -- I knew that it needed to be flipped but didn't know how to do it exactly.
Glad it helped, and feel free to share!
Thank u so much, the only video that made me understand R and S, my professor seems to be the only one in the world to do certain exercises with whole molecules, everyone only does the centers, thanks man
❤❤❤Thank you sooo soooo much! I have an exam this wednesday and I needed to review this!
exactly what i needed, thank you!!
Thanks for watching and feel free to share the video!
Thank you so much! I have been stuck in the wedged H found in ring compounds and didn't know what to do for a while.
Glad I could help!
Thank u very much for this..... I missed the class for this topic in my institute so I came up here.
First molecule would not be Chiral. It has two of the same substitutes (CH3) coming from the same stereogenic center.
You are correct, that was a mistake!
Thank you so much for this amazing video!!
Glad you liked it!
How do we know Br is back and H is forward if we aren't given the wedges (say, we were given the skeleton but everything was lines....)
For the second one wouldn’t we invert the R configuration since the highest priority substituent is the carbon bonded to bromine?
THANK YOU SO MUCH.... This is what I have been looking for....
Glad I could help!
thanku a lot very nice ...
this helped a lot! thank you:)
I'm so glad!
Thank you so much 😭🤲🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻
thank you! very helpful
Thanks for watching and feel free to share the video!
Do you have a little difficult ones?
Thank u very much ❤
What if number 4 and number 1 priority is on the same plane, do we need to convert it?
fakhrul razi yes if it comes R then its S
fakhrul razi no
thanks mate you really helped me out
Thanks for watching and I'm glad it helped!
Thanks that's a lot helpful :)
Glad to hear that!
This helped me thanks a lot
Thanks for watching and feel free to share the video as well!
Thanks !!
Thanks for watching and feel free to share the video!
Cleared my concept....thanku
Glad it helped!
there are no chiral carbons in the first question. All 4 groups need to be different and 2 CH3 are attached
You are correct, that was a mistake!
Thank you
You're welcome!
Thank u
No problem!
thanks mate
Thanks for watching and feel free to share the video!
Watch at 1.5x speed
thanks, ordering carbons never made sense to me
Glad I could help!
only a chiral center if it is bonded to 4 different groups, so this is wrong!
just watched it sry you fixed it
this helped a lot! thank you:)
Thanks for the feedback! We're really glad it helped you out!