STEREOISOMERISM
S.M.TRIPATHI
                                           TOPIC : OPTICAL ISOMERISM
1.     Which of the above descriptions may be applied to these isomeric structural formulae?
           OH                 OH
                   and
       (A)          They are diastereomers                            (B)     They are tautomers
       (C)          They are enantiomers                              (D)     They are identical
2.     A solution of (+)-2-chloro-2-phenylethane in toluene racemises slowly in the presence of a small
       amount of SbCl5, due to the formation of
       (A) Carbanion (B) Carbene                       (C) Free radical              (D) Carbocation
3.             Et
      H3C               OH
                                    has chiral (*)center it is
               H
       (A) R                              (B) S                       (C) both                             (D) none
                                                                 Cl
4.    Number of chiral carbon atoms in                                        is
                                                                 CH3
       (A) 2                              (B) 3                       (C) 4                                (D) 1
5.     Iso pentane, (CH3)2CH.CH2.CH3 can form four isomeric monochloro derivatives. How many these are
       optically active?
       (A) 1                  (B) 2                   (C) 3                 (D) 4
6.     Meso-Tartaric acid is optically inactive due to the presence of
       (a) Molecular symmetry (b) Molecular asymmetry
       (c) External compensation                          (d) Two asymmetric C-atoms
7.     Which of the following compounds is optically active
       (a) CH3CH2COOH           (b) CH3CHOHCOOH         (c) HOOC.CH2.COOH                                  (d) CH3.CO.COOH
8.     The necessary and sufficient condition for a molecule to exhibit optical activity is
       (A) Molecular symmetry                           (B) Molecular dissymmetry or chirality
       (C) Presence of chiral carbon atoms              (D) Tetrahedral nature of carbon atoms
9.     Optical isomers which are non-superimposable mirror images of each other are called
       (A) Enantiomers         (B) Diastereomers     (C) Tautomers           (D) Geometrical isomers
10.    Which of the following statements is not applicable to enantiomers?
       (A) They have identical melting and boiling points
       (B) They have identical chemical properties except towards optically active reagents
       (C) They can be separated by fractional crystallization
       (D) They rotate the plane polarized light in different directions but to the same extents
11.    Which of the following will show optical isomerism?
               Cl            CHBr - CH3                                       H3C              Cl
       (A)          C    C                                             (B)             C   C
               H             Cl                                                  H             CH2 - CH3
               H3C                CH3                                         H3C               H
       (C)              C     C                                        (D)             C   C
                    Br            CH2Br                                            H            CH3
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                                                   STEREOISOMERISM
                                                                                                             S.M.TRIPATHI
12.   What is the possible number of stereoisomers for tartaric acid?
      (A) four                (B) three               (C) two                                      (D) one
13.   Racemic mixture is optically inactive because of
      (A) molecular symmetry                           (B) external compensation
      (C) internal compensation                        (D) molecular asymmetry or chirality
14.   The optical isomers which are not mirror images of each other are called
      (A) diastereomers       (B) Tautomers           (C) Enantiomers          (D) Metamers
15.   The two isomers given below are
           CO2H               CO 2H
       H      OH          H        OH
                    and
      HO      H           H        OH
           CO2H               CO 2H
      (A) Enantiomers         (B) Diastereomers                          (C) Mesomers              (D) Positional isomers
16.   If optical rotation produced by compound(l) is +52o then that produced by compound (ii) is
                                    CH3                         CH3
                              Cl              H           H              Cl
                              H               Cl          Cl             H
                                   CH3                          CH3
                                   (i)                         (ii)
      (A) – 52o               (B) + 52o                                  (C) 0o                    (D) Unpredictable
17.   The correct statements about the compounds A, B, C
                                   COOMe                   COOH                    COOMe
                              H            OH        H           OH           H       OH
                                                                                              is
                              H            OH        H           OH           HO      H
                                   COOH                   COOMe                     COOCH 3
                                   (A)                    (B)                      (C)
      (A) A and B are identical                                          (B) A and B are diastereomers
      (C) A and C are diastereomers                                      (D) A and B are enantiomers
18.   The following two compounds are
                                   CH3                         CH3
                              H            OH        HO              H
                              H            OH        HO              H
                                   C2H5                        C2H5
      (A) Enantiomers         (B) Diastereomers                          (C) Identical             (D) geometrical isomers
19.   An optically active alkene with the M.F. C 6H12 which upon hydrogenation gives optically inactive
      alkane is
      (A) 2-Hexene            (B) 3-Methyl-2-pentene (C) 2-Methyl-2-pentene (D) 3-Methyl-1-pentene
20.   Which of the following does not show enantiomerism?
      (A) 1, 2-propadiene     (B) 2, 3-pentadiene    (C) sec-Butyl alcohol                         (D) All the three above
21.   The configuration at C2 and C3 of the compound given below is
                                   CH3
                              H          Cl
                              Cl         H
                                   C2 H5
      (A) 2R, 3S              (B) 2S, 3R                                 (C) 2S, 3S                (D) 2R, 3R
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                                                 STEREOISOMERISM
                                                                                                               S.M.TRIPATHI
22.   The R-isomer among the following are:
            CHO               H                   CH3                        COOH
      H           OH     D           OH      H             OH      H3C              NH2
            CH 2OH            CH3                 CH 2 - CH 3                 H
            (I)               (II)                (III)                      (IV)
      (A) (i) and (ii)               (B) (i) and (iii)                 (C) (ii) and (iii)           (D) (iii) and (iv)
23.   The specific rotation of a pure enantiomer is +12 o. What will be the observed rotation if it is isolated
      from a reaction with 80% racemization and 20% inversion?
      (A) +9.6o                (B) –2.4o               (C) +2.4o                (D) –9.6o
24.   The lowest molecular weight alkanes which are optically active are
      (A) 3-Methylhexane                               (B) 2, 3-Dimethylpentane
      (C) 2, 3, 3-Trimethylbutane                      (D) 2-Methylhexane
25.   Which of the following have finite dipole moment?
      (A) Propylene           (B) 1-Butene            (C) cis-2-Butene                              (D) trans-2-pentene
26.          The compounds given below are
             HO                   CH3             HO                         CH3
      (A)    Enantiomers                                               (B)          Identical
      (C)    Regiomers                                                 (D)          Diastereomers
27.          The optically active compound among the following is
      (A)          OH                             (B)     O
                      CN
      (C)    HO              OH                                  (D)
                                                                             O
28.          Which of the following compounds is chiral?
      (A)    Br    Br                             (B)                     Br                Br
      (C)    Br          Br                                      (D)      Br
29.   Mark the chiral carbon in Salbutamol
                                                       H
                                                             H
                                                       N         OH          H
                                                                                    H
                                                         H
                                                             H                      OH
                                                                                 OH
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