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Aldehydes Ketones and Carboxylic Acids Test - 28

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Aldehydes Ketones and Carboxylic Acids Test - 28
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Weekly Quiz Competition
  • Question 1
    1 / -0
    Acetic acid is present in vinegar. Curd contains ______ .
    Solution
    Lactic acid is present in curd. The increased acidity causes the milk proteins to tangle into curds. 
  • Question 2
    1 / -0
    _______ is/are used in the manufacture of bakelite polymer.
    Solution
    Phenol and formaldehyde are used in the manufacture of Bakelite polymer.

  • Question 3
    1 / -0
    Formaldehyde is used :
    Solution
    Formaldehyde is used for preserving specimens for the preparation of Urotropine and in manufacture of Bakelite.
  • Question 4
    1 / -0
    How does acetaldehyde react with the following reagents ?
    Solution
    (a) Aldehydes and ketones having at least one $$\alpha$$-hydrogen undergo a reaction in the presence of dilute aqueous caustic soda as catalyst to form $$\alpha$$-hydroxy aldehydes (aldol). This is known as aldol reaction.
    $$\underset{\displaystyle Acetaldehyde}{2CH_3-CHO}\overset{Dil. NaOH}{\rightarrow}\underset{\displaystyle 3-hydroxybutanal}{CH_3-\underset{\underset{\displaystyle OH}{|}}{C}H-CH_2-CHO}\overset{H^+}{\underset{\Delta}{\rightarrow}}\underset{\displaystyle But-2-enal}{CH_3-CH=CH-CHO}$$
    (b) The carbonyl group of acetaldehyde reacts with hydrazine to produce a hydrazone in which the carbon is double bonded to nitrogen.
    (c) When acetaldehyde is warmed with freshly prepared ammoniacal silver nitrate solution, a bright silver mirror is produced. The aldehyde gets oxidized to acetate ion and silver ion is reduced to metallic silver.
    $$CH_3CHO+2[Ag(NH_3)_2]^-+3OH^-\rightarrow \underset{Acetate ion}{CH_3COO^-}+\underset{(silver mirror)}{2Ag}\downarrow+2H_2O+4NH_3$$
    (d) Acetaldehyde on reaction with Phosphorus pentachloride, gives gem-dichloride.
    $$\underset{\displaystyle Acetaldehyde}{CH_3CHO}+\underset{\underset{\displaystyle pentachloride}{\displaystyle Phosphorus}}{PCl_5}\rightarrow \underset{\displaystyle gem-dichloride}{CH_3CHCl_2}+POCl_3$$.
  • Question 5
    1 / -0
    Out of aldehyde and ketones, which is more reactive towards nucleophilic addition?
    Solution
    Aldehydes are usually more reactive toward nucleophilic substitutions than ketones because of both steric and electronic effects. 

    In aldehydes, the relatively small hydrogen atom is attached to one side of the carbonyl group, while a larger $$R$$ group is affixed to the other side. But in ketone, two larger $$R$$ groups are attached to both sides.

    Sterically, the presence of two relatively large substituents in ketones hinders the approach of nucleophile to carbonyl carbon than in aldehydes having only one such substituent. 

    Electronically, two alkyl groups reduce the electrophilicity of the carbonyl carbon more effectively in ketones than in aldehyde.

    Hence Aldehydes are more reactive toward nucleophilic addition reactions than Ketones.
  • Question 6
    1 / -0
    Which of the following is used for preserving biological specimens?
    Solution
    Formaldehyde ($$HCHO$$) in the form of formalin (40% solution of formaldehyde) is used for preserving biological specimens.
  • Question 7
    1 / -0
    Which acid is used in medicine for the treatment of gout?
    Solution
    Methanoic acid is used in treatment of Gout.
  • Question 8
    1 / -0
    Formalin is _______ % solution of formaldehyde in water
    Solution
    Formalin is $$40$$% solution of formaldehyde in water.
    Formalin means $$40$$% formaldehyde.
  • Question 9
    1 / -0
    Benzaldehyde is used:
    Solution
    Benzaldehyde is used as flavoring agent, manufacture of dyes like triphenylmethane dyes and also as starting material for the preparation of cinnamic acid.
  • Question 10
    1 / -0
    ________ is used in the preparation of chloroform, sulphonal, cordite etc.
    Solution
    Preparation of chloroform from acetone is:
    $$CaOCl_2+H_2O\longrightarrow Ca(OH)_2+Cl_2$$
    $$CH_3COCH_3+3Cl_2\longrightarrow CCl_3COCH_3+3HCl$$
    $$2CCl_3COCH_3+Ca(OH)_2\longrightarrow 2CHCl_3+(CH_3COO)_2Ca$$
    Preparation of sulphonal from ketone is shown in IMAGE $$01$$
    Preparation of cordite  is shown in Image $$02$$
    Cordite is a propellant which is addition product of ketone.
    Hence, above all are prepared from acetone.

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