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    Xii-Board 3RD 33% Chemistry DRT - 2 - 20.11.2023

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    1. The document is a chemistry exam for class 12 covering topics like nucleophilic addition reactions, IUPAC naming of organic compounds, order of acidity, aldol condensation reactions, chemical tests to distinguish compounds, and multi-step organic reactions. 2. The exam contains three sections - short answer questions worth 1 mark each, short questions worth 2 marks each requiring explanation of concepts and reactions, and longer answer questions worth 3 marks each involving explanation of organic reactions and multi-step syntheses. 3. The topics covered include properties of aldehydes and ketones, acid-base chemistry, naming organic compounds, tests to distinguish organic compounds, and multi-step named organic

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    Xii-Board 3RD 33% Chemistry DRT - 2 - 20.11.2023

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    lgtv3679
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    1. The document is a chemistry exam for class 12 covering topics like nucleophilic addition reactions, IUPAC naming of organic compounds, order of acidity, aldol condensation reactions, chemical tests to distinguish compounds, and multi-step organic reactions. 2. The exam contains three sections - short answer questions worth 1 mark each, short questions worth 2 marks each requiring explanation of concepts and reactions, and longer answer questions worth 3 marks each involving explanation of organic reactions and multi-step syntheses. 3. The topics covered include properties of aldehydes and ketones, acid-base chemistry, naming organic compounds, tests to distinguish organic compounds, and multi-step named organic

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    XII-BOARD 3RD 33% CHEMISTRY DRT- 2 -20.11.2023

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    1. The document is a chemistry exam for class 12 covering topics like nucleophilic addition reactions, IUPAC naming of organic compounds, order of acidity, aldol condensation reactions, chemical tests to distinguish compounds, and multi-step organic reactions. 2. The exam contains three sections - short answer questions worth 1 mark each, short questions worth 2 marks each requiring explanation of concepts and reactions, and longer answer questions worth 3 marks each involving explanation of organic reactions and multi-step syntheses. 3. The topics covered include properties of aldehydes and ketones, acid-base chemistry, naming organic compounds, tests to distinguish organic compounds, and multi-step named organic

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    28 views2 pages

    Xii-Board 3RD 33% Chemistry DRT - 2 - 20.11.2023

    Uploaded by

    lgtv3679
    1. The document is a chemistry exam for class 12 covering topics like nucleophilic addition reactions, IUPAC naming of organic compounds, order of acidity, aldol condensation reactions, chemical tests to distinguish compounds, and multi-step organic reactions. 2. The exam contains three sections - short answer questions worth 1 mark each, short questions worth 2 marks each requiring explanation of concepts and reactions, and longer answer questions worth 3 marks each involving explanation of organic reactions and multi-step syntheses. 3. The topics covered include properties of aldehydes and ketones, acid-base chemistry, naming organic compounds, tests to distinguish organic compounds, and multi-step named organic

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    of 2

    VELAMMAL BODHI CAMPUS

    “Velammal Knowledge Park”


    THIRD 33% BOARD MODULE EXAM – 2023-24

    Class : XII (DRT-2) Marks : 25


    Date : 20.11.2023 CHEMISTRY Duration : 1 hour

    I. ANSWER THE FOLLOWING QUESTIONS : 𝟓 × 𝟏 = 𝟓𝑴


    1. Which of the following is most reactive in nucleophillic addition reactions?
    a) HCHO b) CH3COCH3 c) CH3COC2H5 d) CH3CHO
    2. What is the IUPAC name of the given compound
    CH 3

    CH 3  C  CH 2  CH 3

    COOH
    a) 2,2-Dimethylbutanoic acid b) 3-methylbutane carboxylic acid
    c) 2-ethyl-2-methylpropanoic acid d) 3-methylbutane carboxyllic acid
    3. Arrange the following acids in order of increasing acidity.
    COOH COOH COOH COOH
    NO2
    (A) (B) (C) (D)

    NO2 OH

    a) A<B<C<D b) B<C<A<D c) C<D<B<A d) C<B<D<A


    4. Assertion : Acetaldehyde undergoes aldol condensation with dil.NaOH.
    Reason : Aldehydes which do not contains -hydrogen undergoes aldol
    condensation.
    a) Both ‘A’ and ‘R’ are correct statements, and ‘R’ is the correct explanation of the
    ‘A’
    b) Both ‘A’ and ‘R’ are correct statements, but ‘R’ is not the correct explanation of
    the ‘A’
    c) ‘A’ is correct, but ‘R’ is incorrect statement
    d) ‘A’ is incorrect, but ‘R’ is correct statement
    5. Assertion : Aldehydes & ketones, both react with Tollen’s reagent to form silver
    mirror.
    Reason : Both aldehydes & ketones contain a carbonyl group.
    a) Both ‘A’ and ‘R’ are correct statements, and ‘R’ is the correct explanation of the
    ‘A’
    b) Both ‘A’ and ‘R’ are correct statements, but ‘R’ is not the correct explanation of
    the ‘A’
    c) ‘A’ is correct, but ‘R’ is incorrect statement
    d) ‘A’ is incorrect, but ‘R’ is correct statement

    1
    II. ANSWER THE FOLLOWING QUESTIONS : 𝟒 × 𝟐 = 𝟖𝑴
    6. Write the products of the following reactions.
    CHO
    O
    a) conc.NaOH b) + H2NNH – CO – NH2 𝐻⨁

    CH2CH3
    KMnO4
    c)
    KOH, heat

    7. Give simple chemical tests to distinguish between the following pairs of


    compounds.
    a) Propanal and propanone b) Benzaldehyde & Acetophenone
    c) Phenol & Benzoic acid
    8. Describe the following :
    a) Cross aldol condensation b) Cannizaro reaction
    c) Decarboxylation
    9. Give reasons for
    a) Benzoic acid is a strong acid than acetic acid.
    b) Presence of Alpha hydrogen in aldehydes & ketones is essential for aldol
    condensation.

    III. ANSWER THE FOLLOWING QUESTIONS : 𝟒 × 𝟑 = 𝟏𝟐𝑴


    10. Explain :
    (a) Etard reaction (b) Rosenmund reduction (c) Wolf-kishner reduction
    11. Describe :
    (a) Aldol condensation (b) Clemmensen reduction (c) HVZ-reaction
    12. An organic compound with molecular formula C 9H10O forms 2, 4-DNP derivative,
    reduces Tollens’ reagent and undergoes Canizzaro reaction. On vigorous
    oxidation, it gives 1, 2-benzenedicarboxylic acid. Identify the compound and write
    the reactions involved.
    13. Complete each synthesis by giving starting material.
    (a) C6 H 5CHO  CH 3CH 2CHO 
    dil.NaOH


    (b) Propanone 
    dil. NaOH

    (c) Write Gatterman-Koch reaction

    ****** ALL THE BEST ******

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