To try everything Brilliant has to offer-free-for a full 30 days, visit brilliant.org/SimplifyingSynthesis/ . The first 200 of you will get 20% off Brilliant’s annual premium subscription.
I'm not sure so be aware, but I think bicycles with n atoms > 11 forming the whole ring favours trans configuration (as you can see the other H is going towards the back). So a squarebicycle would have n = 8 and will favour cis configuration.
To try everything Brilliant has to offer-free-for a full 30 days, visit brilliant.org/SimplifyingSynthesis/ . The first 200 of you will get 20% off Brilliant’s annual premium subscription.
Your channel is an excellent resource for those interested in synthetic organic chemistry. Thank you for all the hard work!
Thank you! I really appreciate it
Could you please explain why the protonation forming the green hydrogen occurs at concave face? 8:00
I'm not sure so be aware, but I think bicycles with n atoms > 11 forming the whole ring favours trans configuration (as you can see the other H is going towards the back). So a squarebicycle would have n = 8 and will favour cis configuration.
At some point in the video every new slide was a WTF-Moment. Really enjoyed it!
At 5:10 when you are talking about oxalyl chloride you are showing a formula for phosgene above the arrow. Other than that it's a great video.
Good spotting, thanks!
Sir make a detail video about tiruchenduramine