Determining R and S Practice

[@kevinceballos8256]

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.

[@learningsimplyvideos]

Glad it helped, and feel free to share!

[@ela9917]

❤❤❤Thank you sooo soooo much! I have an exam this wednesday and I needed to review this!

[@TheTutorTwins]

First molecule would not be Chiral. It has two of the same substitutes (CH3) coming from the same stereogenic center.

[@learningsimplyvideos]

You are correct, that was a mistake!

[@NM-vl5hn]

Thank u very much for this..... I missed the class for this topic in my institute so I came up here.

[@mysteryfacebookgirl]

exactly what i needed, thank you!!

[@learningsimplyvideos]

Thanks for watching and feel free to share the video!

[@OrthodoxCat3472]

For the second one wouldn’t we invert the R configuration since the highest priority substituent is the carbon bonded to bromine?

[@rachaeltang9247]

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....)

[@fakhrulnawawi9681]

What if number 4 and number 1 priority is on the same plane, do we need to convert it?

[@AdityaKrsingh-fb5fj]

fakhrul razi yes if it comes R then its S

[@solankijerry2631]

fakhrul razi no

[@saiajamal4995]

Thank you so much 😭🤲🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻🫶🏻

[@poonamsrivastava5478]

there are no chiral carbons in the first question. All 4 groups need to be different and 2 CH3 are attached

[@learningsimplyvideos]

You are correct, that was a mistake!

[@alexanderg8466]

Do you have a little difficult ones?

[@naveenr4153]

this helped a lot! thank you:)

[@learningsimplyvideos]

I'm so glad!

[@scientium8770]

Thanks that's a lot helpful :)

[@learningsimplyvideos]

Glad to hear that!

[@metrodaisies]

thank you! very helpful

[@learningsimplyvideos]

Thanks for watching and feel free to share the video!

[@salmahossam8148]

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.

[@learningsimplyvideos]

Glad I could help!

[@areenaazlan7001]

THANK YOU SO MUCH.... This is what I have been looking for....

[@learningsimplyvideos]

Glad I could help!

[@KuldeepSingh-tx6jt]

Cleared my concept....thanku

[@learningsimplyvideos]

Glad it helped!

[@muhammeddamilola5600]

Thank you

[@learningsimplyvideos]

You're welcome!

[@w.s.6303]

Thank u very much ❤

[@maryhuang3884]

Thank you so much for this amazing video!!

[@learningsimplyvideos]

Glad you liked it!

[@trappi5443]

thanks mate you really helped me out

[@learningsimplyvideos]

Thanks for watching and I'm glad it helped!

[@satnamkaler1246]

thanku a lot very nice ...

[@beeu7814]

Thank u

[@learningsimplyvideos]

No problem!

[@jacksonreeve9780]

thanks mate

[@learningsimplyvideos]

Thanks for watching and feel free to share the video!

[@humanhuman9228]

This helped me thanks a lot

[@learningsimplyvideos]

Thanks for watching and feel free to share the video as well!

[@pranav7152]

Thanks !!

[@learningsimplyvideos]

Thanks for watching and feel free to share the video!

[@emilycrawford810]

only a chiral center if it is bonded to 4 different groups, so this is wrong!

[@emilycrawford810]

just watched it sry you fixed it

[@Noneofyobusinessdude]

thanks, ordering carbons never made sense to me

[@learningsimplyvideos]

Glad I could help!

[@carlykiller]

Watch at 1.5x speed

[@marebearzzz027]

this helped a lot! thank you:)

[@learningsimplyvideos]

Thanks for the feedback! We're really glad it helped you out!