E2 Reaction

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Enough with substitutions, let's look at eliminations. Bring on the pi bonds! The E2 reaction is a very common one that we will have to understand in mechanism, transition state, and product distribution.

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short and sweet. this video does not drag on

undercoverpotential
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never thought of it as hydrogen bonding. Professor Dave is clutch 👏

amandawramage
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Tommorrow I have organics exam and iam so afraid.

rabrab
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You are soooo helpful for my orgo chem class!!!

menkiguo
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Professor Dave I would like to talk to you about a lot of things!!!! lol

attiamorrison
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Another great video....your intro is priceless!

curtpiazza
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Professor Dave u r the best!! U saved my life thanks so much!!

Kasey-wwoy
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Cool Prof. Dave ... nice and short. Hydroxide ion steals a Hydrogen off beta carbon on Bromopropane molecule, also releasing the Bromine, turning it into Propene. With Water molecule. Thanks. Well done !!

seanbergeron
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I think I understand, but need some reconfirmation. Since the base abstracts H from the beta carbon, in that case a methyl halide does not undergo elimination reactions since there's only the alpha Carbon. And primary, secondary, and tertiary halides undergo E1/E2 depending on weak base/strong base, steric hindrance is not a factor

johnmandrake
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merci! je veux savoir si t'as une video qui explique quand utiliser SN1, E1, SN2, E2 rxns? :-D
je sais que SN2 et E2 sont rxns competitif... egalement pour SN1 et E1.

EmptySequencee
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chemistry is cool when u finally understand something🎉

force_psycho
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What are other conditions for sn1 or e1 to occur other than temperature and ... 

The steric hinderence of reagent and substrate both responsible for sn1 and e1

sarwarpasha
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Is this series..(play list of organic chemistry) sufficient for neet!! Plz answer me

ramyasree
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What does the inequality sign on the corner of the intermediate bracket represent?

eshalshoaib
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I did not understand where did the CH3 came in the transition state, could you please explain?

Britsuuu
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hi professor! what's differences between E1 and E2 reaction?

bellismoaz
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Should have talked about stereochemistry for.this reaction, IMO, even if there's one product. It's always something to keep in mind and double check.

VeritasEtAequitas
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And also if we have strong base
The mechanism follow SN1 or SN2

nourhanhassanabdelnaby
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sir how to differ between sn2 and e2 mechanism because they both uses nucleophile and
R-x type reactant?

adityaagarwal
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Prof. Dave Ji ( In Malayalam Dave = Dev ( The God) . You mechanically acted like God to us guys though. Am from Kerala S. India. Am a Tutor and love to view your videos for finalized notes. Teaching upto plus two. Expecting your valuable videos still. Corona is not a joke. Really creepy when the educational arena is considered. You do rock Sir. Take Care please. Saareeyakal Sir !!!
🙏🙏🙏

mathewjohn