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Aldehydes Ketones and Carboxylic Acids Test - 5

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Aldehydes Ketones and Carboxylic Acids Test - 5
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Weekly Quiz Competition
  • Question 1
    1 / -0

    The aldehydes and ketones undergo one of the following reactions:

    Solution

    Aldehydes and Ketones undergoes the characteristic nucleophilic addition reaction. this is because of presence of polar>C=O bond in aldehydes and ketones. due to electronegativity difference between C and O, O bears a small (delta ) negative charge while C bears a small (delta ) positive charge. now because of delta positive charge on C nucleophile can add to >C=O  bond giving nucleophilic addition reaction

  • Question 2
    1 / -0

    Arrange the following compounds in decreasing order of their acid strength: i) trichloroacetic acid ii) trifluoroacetic acid iii) acetic acid and iv)formic acid

    Solution

    Stronger acid always has a stable conjugate base. If RCOOH is acid and its conjugate base is RCOO-, then the conjugate base of RCOOH  will get stabilised when R group contains electron withdrawing group like F (strong -I effect). Stability of the conjugate base will increase the acidity of acid. While if R group is CH3 which shows electron donation (+I effect), the conjugate base gets destabilised and acidity decreases.

  • Question 3
    1 / -0

    CH3CHO and C6H5CH2CHO can be distinguished chemically by:

    Solution

    CH3CHO will give iodoform test and C6H5CH2CHO will not give iodoform test. Methyl aldehydes or ketones give iodoform test. In carbonyls like RCOR'  one of R or R' should be a  CH3 group to give positive iodoform test.

    CH3CHO + NaOI→ CHI3 + HCOO-Na+

    CHI3 formed is known as iodoform and is yellow precipitate.

    C6H5CH2CHO + NaOI → no reaction

  • Question 4
    1 / -0

    Which of the following acids does not exhibit optical isomerism?

    Solution

    Maleic Acid shows Geometrical Isomerism due restricted bond roation along C=C bond but does not give optical isomerism as it has  horizontal plane of symmetry  , as C=C bond is planar and thus do not form a non superimposable mirror image and is optically inactive .

  • Question 5
    1 / -0

    The compound obtained when acetaldehyde reacts with dilute aqueous sodium hydroxide exhibits:

    Solution

    CH3CHO will react with aq NaOH to give aldol condensation reaction leading to formation of alpha-beta unsaturated aldehyde i.e.CH3CH=CHCHO

    The product which is suitably substituted and has restricted bond rotation along C=C bond and doesn't have any chiral center so it will show only geometrical isomer.

  • Question 6
    1 / -0

    Benzaldehyde and acetone can be best distinguished using

    Solution

    Tollen's Test is used to distinguish between and aldehyde and ketone. It uses the fact that aldehydes are easily oxidised to their corresponding acids while ketones are not.

    Tollen's reagent are aqueous ammonical silver nitrate solution which react with aldehydes as shown.

    RCHO + 2Ag+ + 2OH-  →  RCOO- + Ag + H2O.

    RCOR + 2Ag+ + 2OH  → No reaction

    If this test is carried in glass tube, the Ag formed forms a mirror on the sides of test tube so the test is also known as silver mirror test. 

    Aldehydes show tollen’s test while acetone which is a ketone does not give tollen’s test.

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