H₂C H₂CC H₂C HOT -Br ou CH3 CH3 CH3 Chin CH3 Carbocation intermediate H₂C Cili H₂C -OH + Br HO H₂C CH3 OH can attack front or back side of the carbocation thus both compounds can be formed considering the sterechemistry Name this mechanism (S1, S2, E1, or E2), and describe what is happening in detail. a. What type of solvent would be used in this mechanism and why? b. Write out the full rate law equation for this mechanism.
H₂C H₂CC H₂C HOT -Br ou CH3 CH3 CH3 Chin CH3 Carbocation intermediate H₂C Cili H₂C -OH + Br HO H₂C CH3 OH can attack front or back side of the carbocation thus both compounds can be formed considering the sterechemistry Name this mechanism (S1, S2, E1, or E2), and describe what is happening in detail. a. What type of solvent would be used in this mechanism and why? b. Write out the full rate law equation for this mechanism.
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 53AP
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