the explanation of this was beyond phenomenal. thank you for helping me to understand! wish you were my professor
@aryakaran27433 жыл бұрын
This video is helpful after 6 years too.. thanks for providing the clarity of the topic and being on point... I have my exam day after tomorrow 🙃🙃
@Clutchprep3 жыл бұрын
Glad it was helpful!
@1314Fher5 жыл бұрын
This makes so much more sense now! Thank you so much T.T
@sophiecantelope7133 жыл бұрын
THANK YOU this is what i needed, now where can I find the base catalyzed???
@Clutchprep2 жыл бұрын
Hey there! You can learn that here: www.clutchprep.com/organic-chemistry/epoxide-reactions
@melodymix9495 Жыл бұрын
Thank you
@sweetness5834 ай бұрын
I thought SN2 reactions didn't happen at tertiary carbons.
@Danoroxursox139 жыл бұрын
don't bases, such as Cl-, attack on the least substituted carbon?
@tarunyadav27652 жыл бұрын
Cl- will attack least substituted carbon when it is base catalysed. But in acid catalysed + plus charge on O is unstable so O will break any one bond (that will cause more + charge on carbon atom)
@ramasamykuppusamy79744 жыл бұрын
Is it sn2 or sn1 mechanism
@Clutchprep4 жыл бұрын
Hey there! The nucleophilic attack will be considered SN1 since Cl attacks the more substituted side. :)
@songoku3624 жыл бұрын
Why the nucleophile attack to the most substituted carbon atom
@Clutchprep3 жыл бұрын
The nucleophile attacked the most substituted carbon atom because it has the most positive character. Hope that helps! :)
@SourajeetSahoo2 ай бұрын
How it has the most positive charge ?
@songoku3622 ай бұрын
Due to inductive effect the density of +ve charge increases and makes it unstable which prefers for acid catalyzed reaction thus base attacks easily.@@SourajeetSahoo
@SourajeetSahoo2 ай бұрын
@@songoku362 due to inductive effect +I... positive charge decreases...
@danielgladish25024 жыл бұрын
Good video showing the arrow pushing, but the title says this is "acid catalyzed". You should have your acid reformed in the product no?
@Clutchprep4 жыл бұрын
Hey Daniel! That's correct. Most of the time, mechanisms don't show catalysts being reformed anymore. I hope this helps! :)