DISTINGUISHING TESTS
In
AISSCE, questions of distinguishing tests are compulsorily asked and it awards
you at least 2 marks.
There
is limited number of distinguishing tests in Class XII Chemistry which can be
easily learn and secure marks.
| 
   Name
  of the Test  | 
  
   For which
  compound  | 
  
   What Happen  | 
  
   Reaction  | 
  
   Examples  | 
 
| 
   Iodoform
  Test  | 
  
   This test is performed by the compound having
  Methyl Ketone (CH3CO-) or CH3CH(OH)-.  | 
  
   In the reaction yellow ppt of Iodoform (CHI3)
  is produced.  | 
  
  ![]()  | 
  
   1. Ethanal 2. Propanone 3. Butan-2-one 4. Ethanol 5. Propan-2-ol Etc.  | 
 
| 
   FeCl3
  Test 
  | 
  
   This test is performed by Phenol.  | 
  
   Phenol gives violet colouration with FeCl3
  solution.  | 
  
  ![]()  | 
  
   Phenol  | 
 
| 
   NaHCO3
  Test (Sodium Bicarbonate Test)  | 
  
   This test is performed by Carboxylic acids
  (R/Ar-COOH)  | 
  
   Acid produces brisk effervescence with NaHCO3.  | 
  
  ![]()  | 
  
   All Carboxylic acids such as Ethanoic acid,
  Benzoic acid etc  | 
 
| 
   Tollen’s
  Test (Silver Mirror Test)  | 
  
   This test is performed by Aldehydes
  (Aliphatic/Aromatic)  | 
  
   Aldehydes form Silver Mirror on the inner side of
  test tube when heated with Tollen’s reagent (Ammoniacal Silver Nitrate)  | 
  
  ![]()  | 
  
   All Aldehydes such as Methanal, Ethanal,
  Benzaldehyde etc.  | 
 
| 
   Fehling’s
  Test  | 
  
   This test is performed by Aliphatic Aldehydes.  | 
  
   Aliphatic aldehydes gives reddish brown precipate
  of cuprous oxide when warmed with a few drops of Fehling’s solution.  | 
  
  ![]()  | 
  
   All Aliphatic aldehydes such as methanol, Ethanal,
  Propanal etc.   | 
 
| 
   2,4-DNP
  Test (2, 4 – Dinitrophenyl hydrazine test)  | 
  
   This test is performed by the compounds having
  carbonyl group ( >C=O)  | 
  
   Aldehydes and ketones form yellow or orange
  precipitate of 2, 4 – dinitrophenyl hydrazone when they react with 2, 4 –
  dinitrophenyl hydrazine.  | 
  
  ![]()  | 
  
   All aldehydes and ketones.  | 
 
| 
   Litmus
  Test  | 
  
   This test is performed by carboxylic acids and
  phenols.  | 
  
   All carboxylic acids and phenols turn blue litmus
  red.  | 
  
   | 
  
   All carbylic acids such as Methanoic acid, Acetic
  acid, benzoic acid etc and phenol.  | 
 
| 
   HgCl2  | 
  
   This test is performed by Formic acid. It is used
  to distinguish between Formic other acids.  | 
  
   Formic acid reduces HgCl2 to give white
  precipitate of Hg2Cl2.  | 
  
  ![]()  | 
  
   Methanoic Acid (Formic Acid)  | 
 
| 
   Hinsberg’s
  Test  | 
  
   This test is performed by amines and used to
  distinguish between 1°, 2° and 3° amines.  | 
  
   On treating amines with hinsberg’s reagent
  (benzene sulphonyl chloride)  1° amines gives N- alkyl benzene sulphonamide
  which is soluble in alkali (aq. KOH). 2° amines gives N, N- dialkyl benzene sulphonamide
  which is insoluble in alkali (aq. KOH). 3° amines dosen’t react at all.  | 
  
  ![]() ![]()  | 
  
   1°, 2° and 3° amines.  | 
 
| 
   Carbylamine
  Test (Isocyanide Test)  | 
  
   This test is performed by 1° amines (Aliphatic as
  well as Aromatic).  It is used to distinguish between primary amines
  secondary/ tertiary amines  | 
  
   Primary Amines react with chloroform in presence
  of alcoholic KOH to form foul smelling carbylamines.  | 
  
  ![]()  | 
  
   All primary aliphatic amines and aromatic amine
  such as Ethanamine, Aniline etc.  | 
 
| 
   Azo
  dye Test  | 
  
   This test is performed by 1° Aromatic amines. It is used to distinguish between 1° Aromatic
  amines and 1° Aliphatic amines.  | 
  
   1° Aromatic amines gives Brilliant Yellow. Orange
  or Red coloured dye on treating with HNO2 followed by alkaline
  solution of 2-naphthol. 1° Aliphatic amines gives brisk effervescence of N2
  gas under these conditions.  | 
  
  ![]() ![]()  | 
  
   Aniline forms Orange dye. Ethylamine gives N2 gas and primary
  alcohols.  | 
 
By: Mr. Satyam Kumar Nigam












Thank you very much sir.
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Thanks Komal for your valuable comment.
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ReplyDeleteThis comment has been removed by the author.
DeleteYour welcome.
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