Page 10 - FPGEE Medicinal and Organic Chemistry Q&A Book
P. 10

Krisman



                                                                 19.    How many enantiomers are possible for
                                   H
                                                                 2,3-Dichloropentane?
               4.        CH             C H
                            3             2  5
                                                                       CH 3  CH   CH    CH 2  CH 3
                                  Cl
                                                                             Cl   Cl
                          (sec-Butyl chloride)
                                                                         2,3-Dichloropentane
               a.      1
               b.      2                                         a.     1
               c.      3                                         b.     3
               d.      4                                         c.     4
                                                                 d.     5
               17.     What is the complete name for the opti-
               cally active compound listed below?               20.    Which  of  the  following  is  (R)-3-
                                                                 hexanol?









               a.      (+)-Bromochloroiodomethane
               b.      (S)-Bromochloroiodomethane
               c.      (R)-Bromochloroiodomethane
               d.      (RS)-Bromochloroiodomethane

               18.     In the following compound what would
               be the correct configuration sequence of atoms
               attached to the chiral carbon?

                                   H

                        CH CH      C    C H 5
                                         2
                           3
                             CH    Cl
                                3
                        3-chloro-2-methylpentane
                                                                 a.     fig-1
                                                                 b.     fig-2
               a.      Ethyl > Cl > Isopropyl > H                c.     fig-3
               b.      Cl > Ethyl > H > Isopropyl                d.     fig-4
               c.      Cl > Isopropyl > Ethyl > H
               d.      Isopropyl > Cl > Ethyl > H













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