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Carboxylic Acid...

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  • Question 1
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    Consider the reaction given below,

    Q. 

    The correct observation regarding the above reaction is/are

     

  • Question 2
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    Consider the reaction given below,

    Q. 

    The correct deduction(s) regarding the above reagent is/are

     

  • Question 3
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    Consider the following reaction,

    Q. 

    The correct deduction(s) regarding mechanism of the above reaction is/are

     

  • Question 4
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    Comprehension Type

    Direction : This section contains a paragraph, describing theory, experiments, data, etc. Three questions related to the paragraph have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).

    Passage

    An organic compound A (C7 H16 O) shows both enantiomerism and diastereomerism. Treatment of a pure enantiomer of A with Na2 CrO4 /Dil. H2 SO4 gives B  (C7 H14 O) - Also A on dehydration with concentrated H2 SO4 gives a single alkene C (C7 H14 ). Ozonolysis of C followed by work-up with Zn-H2 O  gives D (C5 H10 O) as one of the product which gives racemic mixture on reduction with NaBH4 .

    Q. 

    The structure of A satisfying the above criteria is

     

  • Question 5
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    An organic compound A (C7 H16 O) shows both enantiomerism and diastereomerism. Treatment of a pure enantiomer of A with Na2 CrO4 /Dil. H2 SO4 gives B  (C7 H14 O) - Also A on dehydration with concentrated H2 SO4 gives a single alkene C (C7 H14 ). Ozonolysis of C followed by work-up with Zn-H2 O  gives D (C5 H10 O) as one of the product which gives racemic mixture on reduction with NaBH4 .

    Q. 

    If B is reduced with LiAIH4 followed by acid hydrolysis will give

     

  • Question 6
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    An organic compound A (C7 H16 O) shows both enantiomerism and diastereomerism. Treatment of a pure enantiomer of A with Na2 CrO4 /Dil. H2 SO4 gives B  (C7 H14 O) - Also A on dehydration with concentrated H2 SO4 gives a single alkene C (C7 H14 ). Ozonolysis of C followed by work-up with Zn-H2 O  gives D (C5 H10 O) as one of the product which gives racemic mixture on reduction with NaBH4 .

    Q. 

    The correct statement regarding the compound D is

     

  • Question 7
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    One integer Value Correct Type

    Direction : This section contains 6 questions. When worked out will result in an integer from 0 to 9 (both inclusive).

    Q. 

    If all the aldehyde isomers of C5 H10 O is independently treated with HCN/NaCN solution, how many of them will give racemic mixture of cyanohydrin?

     

  • Question 8
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    If one molecule of trioxane is heated, how many molecules of formaldehyde would be formed?

     

  • Question 9
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    A mixture containing all isomeric cyclohexanedione is treated with excess of NaHSO3 solution. How many different disulphite salts are formed?

     

  • Question 10
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    Consider the following reaction,

    Q

    How many deuterium would be incorporated in the final product?

     

  • Question 11
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    If glyoxal glycol is treated with a mixture of CH3 MgBr and C2 H5 MgBr in diethyl ether followed by acid hydrolysis, how many different diols would be formed, which are simultaneously optically active?

     

  • Question 12
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    Consider the reaction given below,

    Q. 

    X is formed in which a new ring is formed. How many atoms are present in this new ring?

     

  • Question 13
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    Matching List Type

    Direction : Choices for the correct combination o f elements from Column I and Column II are given as options (a), (b), (c) and (d), out of which one is correct.

    Q.

    Match the reactants from Column I with the reagents and expected outcomes from Column II. Mark the correct option form the codes given below.

     

  • Question 14
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    Match the reactions from Column I with the properties of products from Column II. Mark the correct option form the codes given below.

     

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