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Aldehydes Ketones and Carboxylic Acids Test - 6

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Aldehydes Ketones and Carboxylic Acids Test - 6
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  • Question 1
    1 / -0

    One mole of a symmetrical alkane on ozonolysis gives two moles of an aldehyde having molecular mass of 44u. The alkene is

    Solution

    2-butene on reductive ozonolysis with O3/Zn will give CH3CHO which has molecular mass of 44u.

    CH3CH = CHCH3 + O3/Zn →  2CH3CHO

    Molecular mass of CH3CHO = 12+3+12+1+16 = 44u

  • Question 2
    1 / -0

    Ketones are reduced to the corresponding alcohols by catalytic hydrogenation to form

    Solution

    Aldehydes on catalytic hydrogenation using H2/Pt give primary alcohols while ketones on catalytic hydrogenation using H2/Pt give secondary alcohols.

  • Question 3
    1 / -0

    Which of the following is correct?

    Solution

    I2 in presence of NaOH act as a weak oxidising agent and thus C2H5OH get oxidizes to CH3CHO. and –COCH3 group is important for iodoform .

    CH3CHO + I2 +  OH-  → CHI3 + HCOO-

    CHI3 is a yellow ppt known as iodoform

  • Question 4
    1 / -0

    A mixture of benzaldehyde and formaldehyde on heating with aqueous NaOH solution gives

    Solution

    They will undergo cannizaro reaction as neither benzaldehyde nor formaldehyde has alpha hydrogen.

    HCHO will be more reactive towards cannizaro compared to benzaldehyde because of less steric hinderance.

    So, OH- nucleophile will attck on HCHO first and then hydride shift from HCHO to benzaldehyde will occur. and thus HCHO will oxidise to HCOO- ion and benzaldehyde will reduce to benzylalcohol.

  • Question 5
    1 / -0

    Clemmensen reduction of a ketone is carried out in the presence of which of the following?

    Solution

    For Clemmenson we use Zn-Hg( conc HCl ). This reduction reduces carbonyl groups to alkane. this reduction cannot be used when an acid sensitive group is present.

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