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SN1 Reaction Mechanism
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- Опубліковано 5 сер 2024
- This organic chemistry video tutorial provides a basic introduction into the SN1 reaction mechanism. It explains how to identify the major product and It includes example problems with carbocation rearrangements such as the hydride shift and methyl shift. It discusses the stereochemistry of the SN1 reaction such as the production of an unequal racemic mixture of stereoisomers due to the formation of an ion pair during the ionization of an alkyl halide. It includes many solvolysis reactions with H2O and CH3OH. It discusses substrate reactivity and leaving group stability.
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SN1 SN2 E1 E2 - 4 Hour Test Review:
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Access The Full 1 Hour Video on Patreon: bit.ly/3kIbBmP
SN1 SN2 E1 E2 - 4 Hour Test Review: bit.ly/3Bt4ghw
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These are straight forward concepts and my lecturers notes now make sense after watching this video keep up man!🙏
YOU ARE A LIFE SAVER!!! You made this concept soooo much easier to understand. Thank you so much!!!
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Hi, at 8:10. From step 2 to step 3, the Energy Profile Diagram has shown decrease (endothermic) but during the 3rd step, when OH2+ changes to OH, it becomes more stable and energy is released. So it must be exothermic and the graph must increase at the third transition state.
Thank you as always
This was so helpful! Thank you.
I don’t think you understand how many people you have helped over the years
I think at 21:49 there's a mistake, because the ability of a compound to give SN1 reaction is measured by the stability of the carbocation that's going to be formed IMMEDIATELY after the removal of the old nucleophile as that is the rate determining step and the rearrangement shouldn't be considered in this case, hence the third compund will show most reactivity to SN1 as the carbocation that's going to be formed will have 5 alpha hydrogens for hyperconjugation stabilization
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24:40 Could easier way to find the better leaving group be finding the more stable base/more acidic leaving group?
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14:11 most reactive to sn1
23:05 best substrate for sn1 and sn2
24:40 aryl halides and benzyl halides do NOT work for sn1
25:11 to 26:01 iodide is a better leaving group than bromide as it can stabilize the -ve charge better. larger ions can stabilize a -ve charge better than smaller ions.
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super teaching first comment
Great
24:21
They dont work so we are just supposed to remember this arbitrary rule? No explanation? WOW great lessons here! just remember this random rule !
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can u plz also upload the full 1 hour video on youtube as well? I have joined your Membership Program on youtube but i cannot find this video on youtube, thanks
Here it is: ua-cam.com/video/0JJ_5117lIY/v-deo.html
@@TheOrganicChemistryTutor thank you so much for ur help
at 4:05 wouldn't that carbon be a chiral center ?therefore producing a racemic mixture. anyone please chime in
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9:10 why did it just grow a random leg and H ?????
the h is always there and it is not a random leg, it represents the bond between c and h. the bonds between c and h are often not shown in a line diagram, only the heteroatoms (i.e, atoms other than c and h, like O, N, etc,) are shown differently and named.
12:54
Good luck everybody in finals time
commenting for the algorithm
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First
2:09
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