Sn1, Carbocation Rearrangement, Sn1 vs Sn2 Reaction mechanisms |JEE & NEET 2021 Chemistry| Pahul Sir

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  • Опубликовано: 25 окт 2024

Комментарии • 46

  • @CatalysisbyVedantu
    @CatalysisbyVedantu  4 года назад +8

    Hey people! We hope you enjoyed this awesome session. In case you want to join us as a regular dedicated student in our crash course, enroll at:
    ✅ vdnt.in/jeecce (coupon code PHJEE)
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  • @devidevi-iv4yb
    @devidevi-iv4yb 3 года назад +6

    The great session which i haven't wasted a single SECOND ! 😍 TQ A LOT SIR ji ❤

  • @thunderstorm1748
    @thunderstorm1748 4 года назад +12

    Sir Wonderful session with lots of stuff

  • @sivinvijayan9714
    @sivinvijayan9714 4 года назад +2

    Awesome class sir .. I understood SN 1 mechanism very well.. Thanks a lot!!!!

  • @mylifemydream3275
    @mylifemydream3275 2 года назад

    thank you so much sir...carbocation shift was most easy to understand👍🙏🙏

  • @thomassharma1343
    @thomassharma1343 4 года назад +3

    Thanks sir mind blowing session

  • @tarangnaik2950
    @tarangnaik2950 3 года назад +1

    super awesome lecture sir

  • @anandapatmanabhansu
    @anandapatmanabhansu 3 года назад +1

    Thankyou sir super class.

  • @mehul1217
    @mehul1217 4 года назад +2

    superb class sir.. hats off!

  • @sakshiborkar8024
    @sakshiborkar8024 4 года назад +1

    Uhh r the best sir ♥️ You teach so well ... Your all series are epic 🤟

  • @jadiprabhakar3942
    @jadiprabhakar3942 3 года назад

    Awesome session sir
    Really helped me a lot

  • @harshpreetkaur5701
    @harshpreetkaur5701 4 года назад +5

    50:44 for sn1 will the order be C>D>B>A. ??
    Bcz in C hydride shift takes place which is more favoured than methyl shift in D......?

    • @akshatsachan7810
      @akshatsachan7810 4 года назад +2

      No the order will be D>C>B>A because the RDS is the "formation of carbocation" and hence the rate/reactivity depends upon how stable the first carbocation formed is ..Not on further rearrangement.This is a very important thing to note in SN1 so hope this clarifies any doubts!👍😊

    • @harshpreetkaur5701
      @harshpreetkaur5701 4 года назад +1

      @@akshatsachan7810 but carbocation will be more easily stabilized in C ...thus favouring its formation
      Isn't it?

    • @akshatsachan7810
      @akshatsachan7810 4 года назад +2

      @@harshpreetkaur5701 No, because it can be further rearranged doesn't mean that it will form fast ..For this you have to look to the first carbocation that is forming because Rate only and only depends upon that (not on whether the other one could rearrange to become even more stable than the other one or not) and for the formation of "first" carbocation D is more stable...Hence the order is D>C>B>A. If you have any further doubt you can watch "SN1 reaction in reaction mechanism series of channel "Physics Wallah"👍

    • @harshpreetkaur5701
      @harshpreetkaur5701 4 года назад +1

      @@akshatsachan7810 thanks

  • @AdityaSingh-cl1ru
    @AdityaSingh-cl1ru 4 года назад +1

    Thank you sir , your sessions are really helping in revision :)

  • @vladimirputin965
    @vladimirputin965 3 года назад +2

    sir in last qusstion NH3 is a polar protic solvent right? then SN1 should be major na?🙂

  • @ramareddypadala175
    @ramareddypadala175 3 года назад

    Nice

  • @giridhararaobitragunta4454
    @giridhararaobitragunta4454 3 года назад

    If the phenyl shift does not happen then the carbocation gets satbilize by resonance provided by the benzene ring. But this is not happens why

  • @anandapatmanabhansu
    @anandapatmanabhansu 3 года назад +2

    Sir how can we make all these things useful in real life sir.

    • @awesomechemistry7844
      @awesomechemistry7844 3 года назад +1

      By giving exam and securing a good rank

    • @anandapatmanabhansu
      @anandapatmanabhansu 3 года назад +1

      @@awesomechemistry7844 thankyou bhai can we use this things to solve our common problems.

    • @awesomechemistry7844
      @awesomechemistry7844 3 года назад +2

      @@anandapatmanabhansu YEAH IN GAS LINE COMPANY IN ARAB COUNTRIES TO REDUCE USAGE OF CYLINDER WHICH IS LIKE A MINI BOMB,ALSO IN PETROLEUM RESEARCH IN MANY COUNTRIES ,MANY PRATICAL APPLICATIONS ARE THERE

    • @anandapatmanabhansu
      @anandapatmanabhansu 3 года назад +2

      @@awesomechemistry7844 thankyou bhai we will all study and make it more useful.

  • @Kevin-vk2po
    @Kevin-vk2po 4 года назад

    The example on 37:17 why are we doing that hydride shift? Cause even after the hydride shift we are getting a 2° carbonation only.

    • @harshpreetkaur5701
      @harshpreetkaur5701 4 года назад

      The carbocation formed after shift will be resonance stabilised

  • @abinesh9709
    @abinesh9709 4 года назад

    Sir,are ring expansion and ring contraction important???

  • @rupekapi6259
    @rupekapi6259 3 года назад

    41:00 whether this question show racemic mixture

  • @sunilparekh4581
    @sunilparekh4581 4 года назад +1

    Pls give a heart
    Thanks sir

  • @thomassharma1343
    @thomassharma1343 4 года назад +2

    Sir bs ek guzarish, pehle pura organic khtm krna fir physical, inorganic p ana... Kyunki organic hmara thoda weak h

  • @srijapolepalli2511
    @srijapolepalli2511 4 года назад

    Sir if phenyl is farer than methyl from carbocation in certain compound then what we can take as first preference methyl or phenyl

    • @CatalysisbyVedantu
      @CatalysisbyVedantu  4 года назад +2

      As I said - we look at only the adjacent carbon for the rearrangement

  • @nerengen0054
    @nerengen0054 3 года назад

    10:20 why bromine with a -ve charge with lone pair?

    • @Novanexus234
      @Novanexus234 3 года назад +2

      Bond is made of two electron one from c and other from br as br is more electronegative it will drag electron towards itself so it drag electron of c also .so it gain negative of electron pairs

  • @findtech0
    @findtech0 4 года назад

    9:29

  • @venkatyarasani.3440
    @venkatyarasani.3440 4 года назад +1

    sir,,will the rearrangement takes place in carbo cation during sn1 mechanism????

    • @CatalysisbyVedantu
      @CatalysisbyVedantu  4 года назад +5

      Bro - watch the class carefully and completely please.

  • @sheiknazeera1721
    @sheiknazeera1721 4 года назад +1

    sir in the second question at 55:00 mins
    nh3 is weaker nucleophile than cl-.but why sn2 is major sir please reply

  • @tummalapallivenkataramana5935
    @tummalapallivenkataramana5935 4 года назад +2

    Sir !!
    Please give lecturers on board in the way of art of teaching .....
    I mean by explaining on board by standing
    Sir!!! Please sir it does not mean insulting you sir ...
    Sir!!! Please sir understand .....in that way we can get more interest sir... instead of on computer screen explaning... ..
    Sir !! Please sir teach in that way
    Its not only my opinion sir many others ( my frnds)
    [I mean like way in goc epic]
    Please sir !!!
    🙏🙏🙏🙁🙁🙁🙇🙇🙇

    • @CatalysisbyVedantu
      @CatalysisbyVedantu  4 года назад +4

      Bro - I don't have that huge board at home - we are in lockdown. We shall continue that system once we all can go back to the office to work.
      I hope you can understand the situation and adjust for the time being.

    • @bonisuresh9087
      @bonisuresh9087 4 года назад

      @@CatalysisbyVedantu super

    • @abinesh9709
      @abinesh9709 4 года назад +1

      @@CatalysisbyVedantu We should be thankful that atleast we are getting free quality education at the cost of just sitting at home even during this lockdown period