I'm studying for my MCAT right now, and I just wanted to thank you for your clear, accurate explanations. The way you navigated the concept just stuck on my brain, despite me feeling like I'm on my last straw. I'll be referring to your channel more :)
Because Cis structures are on the same side, so there is a ton of steric strain (steric strain- when large groups (relatively large groups) are next to each other repelling each other).
I'm studying for my MCAT right now, and I just wanted to thank you for your clear, accurate explanations. The way you navigated the concept just stuck on my brain, despite me feeling like I'm on my last straw. I'll be referring to your channel more :)
Glad the channel is helping out - Happy Studying!
Thank you for sharing your wisdom.
You're welcome, Jessica!
Can you do a video on E1 reactions of a cyclic alkene?
Chad runs laps around my actual professor lmao
Glad you found the channel, Marco!
Excellent videos. I appreciate you doing these. Out of curiosity, what textbook is this following?
i love you. thanks for making organic easy❤
Glad the channel is helping.
Thank you ❤
You're welcome
your reference books ?
good job
Thank you
Hello, for the last problem with the Zaitsev rule, why isn't the cis product a major, even if the double bond is also surrounded by 2 carbons?
trans is more stable since the me groups are further away from each other I believe.
Trans more stable cause their dipol moment are negate each other
Because Cis structures are on the same side, so there is a ton of steric strain (steric strain- when large groups (relatively large groups) are next to each other repelling each other).