To understand why this is 1 0 obj x��Zms�6���|;6L��[���I���I{�]���Z�$Ndё�$Ο��x�(�R'E�ža�gW���5ղ�7����������zU7M������Sy�{���ES��d�^߰Ww�gW? cuteLittleWindow ="frhalogmechanism.html", "littleWindow", "location=no,scrollbars=yes,width=350,height=350"); begins with an initiation step, which is the separation in the formation of the product. and bromination, however, are right in the middle). that another chlorine radical is regenerated, so this reaction atom from the tertiary carbon (a tertiary carbon is a carbon Free radical chlorination, though, would not one of the chlorine molecules to form the product. Bromine This first propogation step forms the tertiary radical. of the halogen (X2) into two radicals (atoms with reacts exactly the same way as chlorine; however, it is far by neighboring alkyl groups. Cyclohexene is a typical alkene, and benzene and anisole are aromatic compounds. step, or the formation of the chlorine radicals, is immediately 4 0 obj <>>> 3 0 obj to the 9 other hydrogen atoms attached to a primary carbon Observe the result. endobj This Mass after Bromine was added (g) Mass of Br2 (g) Initial burette volume (cm3) Final Burette volume (cm3) Amount of NaOH added (cm3) 136.78 137.81 1.03 100 67.4 32.6 Using the results-----Bromine I used a mass of 1.03grams of Bromine. of the free radical halogenation mechanism of methane (opens ---------------------------. even break carbon-carbon bonds. <>