methycyclohexene? b. Mtivlohexene because it forms a carbocation when protonated
ID: 542447 • Letter: M
Question
methycyclohexene? b. Mtivlohexene because it forms a carbocation when protonated. bityeyclohexane because the 1' and 3 carbocations are very different in c. Methyl enecy d. 1-Methhexane because the exocyelic double bond is more sterically accessible. exene because the 3° is more stable than the other possible () carbocation e. The product mixture would be too elose to 1:1 (50:5o) to distinguish a mechanism 22. What is the major product of the reaction shown when the starting material is treated with only one equivalent of HBr? HCI d. b. c. 23. What is the major product of the reaction CH,CH.CH,C.CH + H.O + Hgso, + Haso. CI CI Cl C. e. None of the above. 24· The rate for the reaction A + B C a. depends on the concentrations of A and B. b. can be written as rate kAIB] c. will be dependent on the activation energy d. All of the above are true. e. None of the above is true. 25-27.Refer to the illustration to answer questions 25 27. 25 The ordinate (y-axis) "C in the graph shown a. represents increasing ent b. represents the progress of the reaction c represents increasing energy d. represents the equilibrium position of the reaction coordinate e. None of the above is correct.Explanation / Answer
22) answer: b
it is electrophilic addition reaction
23) answer: e.none of the above
because in the reactants, there is no Cl.but in the option all are having Cl.
24) answer: d.All of the above are true.
25) from graph on y-axis, it should be energy
answer: c. represents increasing energy
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