SN2, SN1, E2, and E1 reactions (6)

[00aseel00]

these video's are really useful thank you so much :)

[SphereMaster001]

So that's why secondary and tertiary alpha carbons can only be sn1... brilliant, my teacher never taught me this.

[alexvallerand]

What about hydride shift??? that would make a secondary carbocation which is pretty stable, and we also have poor nucleophile favouring that procedure?

[christoph300]

@alexvallerand To do a hydride shift at all you would first have to have the carbocation. The carbocation will not take place in this situation at all.

[nodollarsign]

holy cow, you are so patient!

[Ms12213]

pure awesomeness!!!



[imaqt012792]

If i get a B I will donate 50 dolars.....

[CountryHearthRome]

@imaqt012792

Test thurs if I get an A I'm donating 25 brah

[matt22us]

Behold the almighty magic cheat sheet lol

[BananaPuddin]

thankyou.

[0new0giga0]

can anyone please give me the exact pdf link to the handout referred here ? i am so lost T.T

thank you..

[kujazero]

@0new0giga0 read the video description

[m0nchi3]

When carbon chains are electron donors to stabilize a carbocation, is that the same thing as hyperconjugation?

[TheJamesTopham]

@m0nchi3 yes

[ctoth666]

no resonance in the secondary carbocation after the shift maybe?

[bd1322]

n00bs VVVVVVVVVVV

[kortniscott]

what about methyl radicals?

[whatevergirlyman]

why cant there be a hydride shift?

[pcbjunkie]

i think the primary carbon is way too unstable to allow it to happen

[EternalxJourney]

@whatevergirlyman yea i was wondering the same thing. why can't the beta hydrogen shift to the alpha carbon to produce a secondary carbocation?