13.3 & 13.4 Reactions of Alkenes and Electrophillic Addition

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AS - Level Chemistry (13 - Alkenes) Mindmap am 13.3 & 13.4 Reactions of Alkenes and Electrophillic Addition, erstellt von Bee Brittain am 10/03/2016.
Bee Brittain
Mindmap von Bee Brittain, aktualisiert more than 1 year ago
Bee Brittain
Erstellt von Bee Brittain vor mehr als 8 Jahre
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Zusammenfassung der Ressource

13.3 & 13.4 Reactions of Alkenes and Electrophillic Addition
  1. Addition reactions of the alkenes
    1. Hydrogen Halides
      1. Alkenes react with gaseous hydrogen halides at room temp to form haloalkanes
        1. If alkene is gaseous, reaction take place when two gases are mixed
          1. If alkene is liquid, the the hydrogen halide is bubbled through it
            1. Alkenes can also react with concentrated HCl or HBr (which are solution of the hydrogen halides in water)
          2. Each of these reactions involves the ADDITION of a small molecule across the double bond, causing the pi bond to break, and new bonds to form
            1. Hydrogenation of Alkenes
              1. Nickel Catalyst
                1. 423K
                  1. Alkene + Hydrogen = Alkane
                    1. Hydrogenation of Propene >>
                    2. Hydration reactions of Alkenes
                      1. Alkene + Water (steam) --> Alcohol
                        1. Requires the presence of a phosphoric acid catalyst (H3PO4)
                          1. Can form a Primary or secondary alcohol
                        2. Halogenation
                          1. Rapid addition reaction with the halogens: Cl or Br at room temperature
                            1. Haloalkane
                        3. Electrophilic addition in Alkenes
                          1. Alkenes usually take part in addition reactions to form saturated compounds = ELECTROPHILLIC ADDITION
                            1. Double bond in an alkene represents region of high electron density due ton presence of pi-electrons
                              1. High electron density attracts electrophiles
                                1. Electrophile = An atom that is attracted to an electron-rich centre and accepts an electron pair. Usually a positive ion or molecule containing an atom with a partial positive charge.
                              2. ^^ The mechanism
                            2. Markownikoff's Rule
                              1. You can have a primary or secondary carbocation. This is similar to a primary or secondary alcohol.
                                1. Carbocation Stability
                                  1. The stability increases as you go from primary carbocation, through to tertiary carbocation.
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