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Why arent part 1 and 3 E2 reactions? Doesnt E2 have strong bases as a part of their mechansim?
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- What is the best way to remeber the differences between Sn1, Sn2, E1 and E2 reations?Use the chair confirmation to explain the regio chemistry of the E2 reaction and then draw the product using both the chair and dash/wedge models.The E2 reaction is defined as stereoselective if the reacting alkyl halide contains? The E2 reaction is defined as regioselective if the reacting alkyl halide contains? only one β-hydrogen. two β-hydrogens attached to the same β-carbon atom. ...two β-hydrogens attached to different β-carbon atoms. ...no β-hydrogens.
- Explain the difference between Zaitsev elimination and Hoffman elimination in E2 reactions. What conditions favor each? Why? Are these examples of stereoselectivity or regioselectivity? Explain. Which is always favored in an E1 reaction.SN1 reactions are better performed in protic solvents. Explain why the researchers could not perform the reaction using 100% water as solvent instead of 50% aqueous acetone.Use curved arrows to show the movement of electrons in the attached E2 mechanism. Draw the structure of the transition state.