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Aldehydes Ketones and Carboxylic Acids Test - 37

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Aldehydes Ketones and Carboxylic Acids Test - 37
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  • Question 1
    1 / -0
    Which of the following compounds will give butanone on oxidation with alkaline $$KMn{O}_{4}$$ solution?
    Solution

  • Question 2
    1 / -0
    Structure of $$(x)$$ is:

    Solution
    The above reaction is called aldol condensation reacation.

  • Question 3
    1 / -0
    (i) $$H_3C-\overset{O}{\overset{||}{C}}-CH_3$$
    (ii) $$H_3C-\overset{O}{\overset{||}{C}}-CH_2-\overset{O}{\overset{||}{C}}-CH_3$$
    (iii) $$Ph-OH$$
    (iv) $$H_3C-\overset{O}{\overset{||}{C}}-OH$$

    Among the compounds the correct order of $$pKa$$ values are:
    Solution
    Carboxylic acid is stronger than alcohol than active methylene compound because of its stability.
    Acid = $$ 4>3>2>1$$
    $$pKa \propto \cfrac{1}{acid} = 1>2>3>4$$

  • Question 4
    1 / -0
    Most acidic hydrogen is present in :
    Solution
    D has the most acidic Hydrogen.
    Since the stability of negative charge determines acidity, so oxygen being more electronegative, the negative charge on it is more stable than on carbon.
  • Question 5
    1 / -0
    $$C$$. Compound $$(3)$$ is:

    Solution

  • Question 6
    1 / -0
    An organic compound containing $$-COOH$$ functional group is called:
    Solution
    The compound containing $$-COOH$$ as the functional group are called the carbonyl group. These groups are polar in nature because it acts both as hydrogen bond acceptor and hydrogen bond donors.
  • Question 7
    1 / -0
      

    Solution
    Since $$LiAlH_4$$ is very strong reducing agent, it reduces $$\alpha - \beta$$  unsaturated double bond also of aldehyde due to strong polarization towards double bond.

  • Question 8
    1 / -0
    The suitable reagent(s) will be:

    Solution
    Since aldehyde undergo fast silver mirror test to give corresponding acids and other groups do not react with Tollen's reagent, so it is better.
    $$R - CHO \xrightarrow{[Ag (NH_3)_2 ^{\oplus}] OH^-} R - COOH$$
  • Question 9
    1 / -0
    Corrosive sublimate ($$Hg{Cl}_{2}$$) can be used to distinguish between:
    Solution
    Option $$B$$ is the correct answer.
    Formic acid gives white precipitate with $$HgCl_2$$ but acitic acid does not react.
    $$HCO_2H+2HgCl_2\longrightarrow \underset{\text{white precipitate}}{Hg_2Cl_2\downarrow} +2HCl+CO_2\uparrow$$
    $$CH_3COOH\xrightarrow[]{HgCl_2}\text{ No precipitate of }Hg_2Cl_2$$
    Formic acid acts as a reducing agent.
  • Question 10
    1 / -0
    Odd one out among the following is:
    Solution
    Since all are acid having $$COOH$$ functional group except Prussic acid which is $$HCN$$.
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