Wednesday, October 31, 2018

WORK Data 271 - Jerry March insurance .....he E1 and E2 elimination Reactions Friedel–Crafts reaction .... Carbocation Rearrangements -




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Below,    
explains  key word concepts --> 


Jerry March insurance
.....  the E1 and E2 

elimination Reactions  


Friedel–Crafts reaction 

....  Carbocation Rearrangements -


Sharon Tate neuroscience explains
atomic continuum communications
and  acetate THOUGHTS 

 - Wikipedia

https://en.wikipedia.org/wiki/Sharon_Tate
    Sharon Marie Tate Polanski (January 24, 1943 – August 9, 1969) was an American actress and model. During the 1960s, she played small television roles before appearing in films and was regularly featured in fashion magazines as a model and cover girl. After receiving positive reviews for her comedic and dramatic ...



    Elton John  and his atomic message system  - Wikipedia

    https://en.wikipedia.org/wiki/Elton_John
      Sir Elton Hercules John, CBE is an English singer, pianist, and composer. He has worked with lyricist Bernie Taupin as his songwriting partner since 1967; they have collaborated on more than 30 albums to date. In his five-decade career Elton John has sold more than 300 million records, making him one of the best-selling ...



      E2 Elimination - E2 stereoselective is loaded - ChemTube3D

      www.chemtube3d.com/Elimination%20-%20E2%20stereisomers.html
        E2 elimination. As you can see from the reaction below, when 2-bromobutane undergoes an E2 reaction, two possible stereoisomers are formed. This is because 2-bromobutane has two conformations with H and Br anti-periplanar, but the one that is less hindered forms the major product, so the E-alkene predominates.





        Elimination reaction - Wikipedia

        https://en.wikipedia.org/wiki/Elimination_reaction
          Jump to E2 mechanism - An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one or two-step mechanism. The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction.

          Comparing the E1 and E2 Reactions — Master Organic Chemistry

          https://www.masterorganicchemistry.com/2012/.../comparing-the-e1-and-e2-reactions/
          Oct 10, 2012 - Remember this reaction – where one elimination gave the “Zaitsev” product, whereas the other one did not. Can you see why now? So what's going on here? The first case is an E2 reaction. The leaving group must be anti to the hydrogen that is removed. e1-e2-ring-e2. The second case is an E1 reaction.



          2003 E2 nightclub stampede - Wikipedia

          https://en.wikipedia.org/wiki/2003_E2_nightclub_stampede
            The E2 nightclub stampede occurred on February 17, 2003, at the E2 nightclub located above the Epitome Chicago restaurant at 2347 South Michigan Avenue in Chicago, Illinois, in which 21 people died and more than 50 were injured when panic ensued from the use of pepper spray by security guards to break up a fight.




            Friedel–Crafts reaction  with Fidel Castro and Cuba - Wikipedia

            https://en.wikipedia.org/wiki/Friedel–Crafts_reaction
              The FriedelCrafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring. There are two main types of FriedelCrafts reactions: alkylation reactions and acylation reactions. Both proceed by electrophilic aromatic substitution.








              Carbocation - Wikipedia

              https://en.wikipedia.org/wiki/Carbocation
                Hyperconjugation is also a stabilizing factor for carbocations. The empty pi orbitals of the carbon atom accepts a pair of electrons from the alpha carbon which then acquires the positive charge. More alpha hydrogens increases the stability of carbocation.

                [PDF]Carbocations - UCLA.edu

                www.chem.ucla.edu/harding/tutorials/cc.pdf
                  carbocation is molecule having a carbon atom bearing three bonds and a positive formal charge. Carbocations are generally unstable because they do not have eight electrons to satisfy the octet rule. B. Carbocation Classification.







                  Carbocation Rearrangements - Chemistry LibreTexts

                  https://chem.libretexts.org/Core/Organic.../E1.../Carbocation_Rearrangements
                    Apr 2, 2014 - Carbocation rearrangements are extremely common in organic chemistry reactions are are defined as the movement of a carbocation from an unstable state to a more stable state through the use of various structural reorganizational "shifts" within the molecule. Once the carbocation has shifted over to a ...

                    The Two Cultures - Wikipedia, the free encyclopedia

                    https://en.wikipedia.org/wiki/The_Two_Cultures
                    Wikipedia
                    The Two Cultures is the title of the first part of an influential 1959 Rede Lecture by British scientist and novelist C. P. Snow. Its thesis was that "the intellectual life of the whole of western society" was split into the titular two cultures — namely the sciences and the humanities — and that this was a major hindrance to solving the world's problems. ...
                    Snow's position can be summed up by an often-repeated part of the essay:
                    A good many times I have been present at gatherings of people who, by the standards of the traditional culture, are thought highly educated and who have with considerable gusto been expressing their incredulity at the illiteracy of scientists. Once or twice I have been provoked and have asked the company how many of them could describe the Second Law of Thermodynamics. The response was cold: it was also negative. Yet I was asking something which is the scientific equivalent of: Have you read a work of Shakespeare’s?


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