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How does changing the halide from (CH3)3CBr to CH3CH2CH2Br affect the rate of an E1 reaction?
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- What is the major organic product of the following E2 reaction? Br CH,CH,ONa ? CH,CH,OHConsider the attached E2 reaction What happens to the reaction rate with each of the following changes?[1] The solvent is changed to DMF. [2] The concentration of −OC(CH3)3 is decreased. [3] The base is changed to −OH. [4] The halide is changed to CH3CH2CH2CH2CH(Br)CH3. [5] The leaving group is changed to I−.Give one example of elimination reaction (E2) type. Show the reactants materials and the product. Draw the reaction mechanism?
- Answer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂OCan you explain the mechanism for this question HO OH H2SO4 cat. H₂ODrawing the SN1 and E1 Products in a ReactionDraw the SN1 and E1 products formed in the reaction of (CH3)3CBr with H2O.
- Draw an energy diagram for the following SN2 reaction. Label the axes, the starting materials, and the product. Draw the structure of the transition state.Which alkyl halide will react the fastest in an SN2 reaction (CH3)3CI CH3CH2Br CH3CH2I CH3I CH3BrDraw the structure (including stereochemistry) of an alkyl chloride that forms each alkene as the exclusive E2 elimination product.
