Page 12 - FPGEE Medicinal and Organic Chemistry Q&A Book
P. 12

Krisman



                                                                 28.    Which of the following C H  isomers
                                                                                                 8  16
                                                                 is thermodynamically most stable?












               a.      i
               b.      ii
               c.      iii
               d.      iv                                        a.     R
                                                                 b.     S
               26.     How     many     stereoisomers     of     c.     T
               (CH ) CHCH=CHCH CH(OH)CH Br are pos-              d.     U
                    3 2             2            2
               sible?
                                                                 29.    How many stereoisomers are possible
               a.      5                                         for the following compound?
               b.      4
               c.      2
               d.      0


               27.     A C H O optically active alcohol (3,3-
                          7  14
               Dimethylcyclopentanol) is oxidized by Jones’
               reagent to an optically inactive (achiral) ketone.
               What is the correct structural formula for this
               compound?                                         a.     2
                                                                 b.     4
                                                                 c.     8
                                                                 d.     10


                                                                 30.    Which of the following compounds has
                                                                 the highest boiling point?

                                                                 a.     CH CH CH CH CH
                                                                           3   2   2   2   3
                                                                 b.     CH CH OH
                                                                           3   2
                                                                 c.     CH Cl
                                                                           3
                                                                 d.     NH
                                                                           4


               a.      1
               b.      2
               c.      3
               d.      4




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