Great Video Josh! However, speeding it up to 1.5 speed recommended for more experienced viewers that just want a refresh of memory. Keep up the good work!
The explanation is very good. However I think the Bürgi-Dunitz-trajectory was drawn incorrectly. It is 107° from the carbonyle, not from the largest substituent. It shouldn't change the outcome though.
Wonderful video!
thank you Josh!!! you are the best
amazing explanations
thank you so much sir, I was having so many difficulties to understand this but now everything is crystal clear
Legend. Taking advanced ochem right now and this is super helpful
very well explained! thank you Josh
Good video only wished u used the Newman projection for the last example
Awesome video, great explanations! :)
How do I know which transition model to use when determining stereoselective products?
very interesting and informative. Thanks
Great Video Josh! However, speeding it up to 1.5 speed recommended for more experienced viewers that just want a refresh of memory. Keep up the good work!
Thanks! If you select the "gear" tool at the bottom of the TH-cam video you can choose your desired playback speed.
Isn't it anticlockwise the first example?
The explanation is very good. However I think the Bürgi-Dunitz-trajectory was drawn incorrectly. It is 107° from the carbonyle, not from the largest substituent. It shouldn't change the outcome though.
Super helpful !
Merci
buenas tardes