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Isomerism Test ...

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  • Question 1
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    Direction (Q. Nos. 1 - 6) This section contains 6 multiple choice questions. Each question has four
    choices (a), (b), (c) and (d), out of which ONLY ONE option is correct.

     

    Q.

    A pure enantiomer with molecular formula C6H13OBr, when reacted with PBr3, an achiral product C6H12Br2 is obtained that has no chiral carbon. The compound which satisfy this condition could be (no bond to chiral carbon is broken during the reaction)

  • Question 2
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    Optical rotation of a newly synthesised chiral compound is found to be +60°. Which of the following experiment can be performed to establish that optical rotation is not actually -300°?

  • Question 3
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    How many stereoisomers exist for the compound 4-(1- propenyl) cyclohexane ?

  • Question 4
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    what is incorrect regarding cis -1, 3-dibromo - trans-2,4-dichlorocyclobutane ?

  • Question 5
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    consider the following zonolysis reaction

    The correct statement about the above product formed is

  • Question 6
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    A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?

  • Question 7
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    Direction (Q. Nos. 7-11) This sectionis based on statement I and Statement II. Select the correct answer from the code given below
    Q. 
    Statement I A racemic mixture is optically inactive.
    Statement II Racemic mixture contain a pair of enantiomers. 

  • Question 8
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    Q.

    Statement I Cis-1,4-dichlorocyclobutane is optically inactive.
    Statement II It possesses plane of symmetry. 

  • Question 9
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    Statement I 2,3-pentadiene is enantiomeric.
    Statement II Enantiomers of 2,3-pentadiene are non-interconvertible due to very large rotational barrier. 

  • Question 10
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    Q.

    Statement I : The Compound shown below is optically inactive.

    Statement II Compound shown above possesses axis of rotation.

  • Question 11
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    Q.

    Statement I Decreasing length of sample tube, while keeping everything else intact, decreases the magnitude of optical rotation.
    Statement II Decreasing length of sample tube decreases the contribution of sample tube material to the total optical rotation. 

  • Question 12
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    Direction (Q. Nos. 12-13) Choice the correct combination of elements and column I and coloumn II  are given as option (a), (b), (c) and (d), out of which ONE option is correct.

    Q.

    Consider the molecules in Column I and match them with their stereochemical properties from Column II

  • Question 13
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    Match the stereochemical terms in column I with their description in column II

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