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This Concept Map, created with IHMC CmapTools, has information related to: FF_Elimination, <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mmultiscripts> <mtext> X </mtext> <mtext> 2 </mtext> <none/> </mmultiscripts> <mtext> elimination </mtext> </mrow> </math> are both single step reactions, single step reactions require either strong bases, Elimination Reactions include <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mmultiscripts> <mtext> H </mtext> <mtext> 2 </mtext> <none/> </mmultiscripts> <mtext> O elimination </mtext> </mrow> </math>, Elimination Reactions include HX elimination, single step reactions require either a good leaving group, carbocation intermediate only if the substrate is secondary or tertiary, unsaturated products all comply with Saytzeff rule, leaving group as usual is a non-metal, a non-metal e.g. <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mtext> -O </mtext> <mmultiscripts> <mtext> H </mtext> <mtext> 2 </mtext> <mtext> + </mtext> </mmultiscripts> <mtext> , -Br </mtext> </mrow> </math>, Elimination Reactions generate unsaturated products, Saytzeff rule leading to more branched products, <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mmultiscripts> <mtext> H </mtext> <mtext> 2 </mtext> <none/> </mmultiscripts> <mtext> O elimination </mtext> </mrow> </math> takes always two steps, Elimination Reactions include <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mmultiscripts> <mtext> X </mtext> <mtext> 2 </mtext> <none/> </mmultiscripts> <mtext> elimination </mtext> </mrow> </math>, Elimination Reactions require substrates with suited leaving group, <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> <mmultiscripts> <mtext> H </mtext> <mtext> 2 </mtext> <none/> </mmultiscripts> <mtext> O elimination </mtext> </mrow> </math> leads everytime to carbocation intermediate, HX elimination are both single step reactions