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- 2. The bromination of 2-butene is an exergonic reaction. H3C + HC. CH, Br. CH Br a. Draw the mechanism for the reaction (you may ignore the stereochemistry for this question). b. In the mechanism drawn above, identify any intermediates. Progress of the reaction Progress of the rea ction c. How many transition states are involved in the above mechanism?. Without drawing the transition state(s), indicate where they occur in the mechanism. Each step of the mechanism of reaction involves a transition state, therefore, Here there are two transition states, each with its own activation energy. d. Which of the following reaction co-ordinate diagrams best illustrates this reaction?.Explain briefly, On the diagram, draw the structures of the reactants, products and intermediates at the correct locations on the diagram and indicate which position(s) correspond to the transition Progress of the readion Progress of the reaction state(s).Draw the structure for the transition state in each reaction. (see the attachment)What is the complete mechanism of this reaction?
- 7. The following data were collected for the reaction: (CH;);CBr + OH- (CH),СОН + Вr- trial [(CH;) CBr] [OH] rate of reaction (mol L-' s-') 1 0.50 M 0.050 M 0.0056 1.00 M 0.050 M 0.011 3 1.00 M 0.10 M 0.011 4 1.50 M 0.050 M 0.017 Determine the form of the rate law and calculate k, the rate constant. You must include units with your answer! Feel free to use any space above to determine relative concentrations/rate, but it's not required.1. What is final product? 2. What are the 4 reactions & steps in mechanism (show product and mechanism steps)? 3. It is kinetic or thermodynamic?Which Transition state would have the lowest energy of activation for an Sn1 reaction? Transition State A Transition State B Transition State C H3C H H3C H;C. H --Br --Br ------Br H3C H H;C
