Organic Chemistry 1 Final Exam Review

[@XxHaRtBrEaKxX]

Thank you! This was everything I really needed to go over again.

[@chemistrytutoring7319]

Hope you did great on your final! :)

[@MobyDrip]

7:51 I'm so confused. How is that achrial? I can't see the line of symmetry.

[@bugfighter5949]

It's achiral because there's no carbon bonded to 4 different groups.

[@MobyDrip]

​@@bugfighter5949A chiral center and a chiral molecule are 2 different things. Molecules can be chiral without having chiral centers and can have chiral centers without being chiral. Looking back on this a year later, it's Achrial because there is no line of symmetry. The 4 carbon substituents on the edges aren't the same. If they were, we would have been able to super impose the image, making it chiral.

[@christopheromoya535]

Great work...keep it going

[@nickharris6848]

Hi wouldn't the (1R,2S,5R)-2-isopropyl-5-methylcyclohexanol actually be (1R,2R,5R)--2-isopropyl-5-methylcyclohexanol due to the Isopropyl substituent being in the back while the implied Hydrogen is in the front?

[@lailaroman5233]

no, because the carbon with the OH group gets 1st priority

[@kehleechan]

it would 'technically' be R but since the Hydrogen will be on a wedged, it becomes an S instead

[@1829Emily]

Thank you! this really helped.

[@ibravol1413]

this is really helpful tqq.

[@chemistrytutoring7319]

I'm glad you found the video helpful! :)

[@araafmannan5065]

ur voice is beautiful bruh

[@anakinskywalker4530]

Thank you so much

[@deathgleam3053]

U sound so dreamy 😍 ✨

[@mankishijosephinepollenjoj7453]

Me watching

[@itsrhoda7757]

this has to be the worst explanation

[@hello-rq8kf]

that's why the title said "review" idiot, she's not gonna teach your lazy ass the entire course

[@joem8251]

I thought it was thorough and helpful in many areas. I'm surprised you think that.

[@yusufzahran726]

Had to stop watching because your voice sounded too congested

[@cjod7652]

Your loss cos she did a good job