Outstanding

God bless you

Thank you so much! Now I understand 😃

thanks a lot

I'm wondering about the last example as I don't know if there's an error or not. How is the primary attached to the tertiary less reactive than the two secondary Carbons? I understand that a tertiary is the least reactive but, secondary are less reactive then a primary and going by the first Carbon, the two secondaries I believe should be less reactive. So my understanding numbering left to right in decreasing reactivity 3>2>5>4>1

thank you so much i almost thought I WAS supposed to attack the substrate, this rly cleared things up!

@DahAcademy

3 жыл бұрын

there never was a substrate.... :|

in the section that u compare nucleophilicity, why does (CH3)3 COH not have a negative charge on the oxygen? Isn't H positive so that would indicate that O is negative? Thanks!

the more polarizible trend going down the column in the periodic table is only true in polar protic solvents. I think it is the opposite for polar aprotic solvents.

This is for polar protic solvent?

I’m the first to watch this video

Do you have any fro SN1, carbocations, carbanions, or radical ranking?

@DahAcademy

3 жыл бұрын

Yes, there’s a playlist called Organic Chemistry 1. You should be able to find some there