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This Concept Map, created with IHMC CmapTools, has information related to: elimination_reactions, more branched structure in accordance with Saytzeff rule, Leaving group 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> </mrow> </math>, single step on vicinal dihalides require a strong base, single step on R-X substrates (monosubstituted) require either a strong base, Elimination Reactions can be single step on R-X substrates (monosubstituted), a very good leaving group 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> </mrow> </math>, Elimination Reactions can be single step on vicinal dihalides, unsaturated products more stable if having more branched structure, through an intermediate carbocation only possible on secondary or tertiary substates, single step on vicinal dihalides require an active metal as Zn, Leaving group is a non-metal, i.e. a nucleophyle, Leaving group e.g. -Br, Elimination Reactions requires presence of a Leaving group, Elimination Reactions generate unsaturated products, single step on R-X substrates (monosubstituted) require either a very good leaving group, Elimination Reactions can be through an intermediate carbocation