Organic Reagents and their uses/functions
| 
   S.No.  | 
  
   Name of
  Reagent  | 
  
   Use/Function  | 
  
   Example  | 
 
| 
   1  | 
  
   HCl + ZnCl2
  (Lucas Reagent)  | 
  
   Substitution of –OH by -Cl group (Alcohol
  to Alkyl Chloride)  | 
  |
| 
   2  | 
  
   HBr or NaBr
  +H2SO4  | 
  
   Substitution of –OH by -Br group (Alcohol
  to Alkyl Bromide)  | 
  |
| 
   3  | 
  
   Red P/X2,
  (X2 = Br2, I2)  | 
  
   Substitution of –OH by –Br/I group (Alcohol
  to Alkyl Bromide/Iodine)  | 
  |
| 
   4  | 
  
   SOCl2  | 
  
   Substitution of –OH by -Cl group (Alcohol
  to Alkyl Chloride)  | 
  |
| 
   5  | 
  
   PCl5  | 
  
   Substitution of –OH by -Cl group (Alcohol
  to Alkyl Chloride)  | 
  |
| 
   6  | 
  
   Cl2
  / Br2 in UV light/hν/heat  | 
  
   Substitution of hydrocarbon by –Cl/Br via
  free radical mechanism (Alkane to Alkyl Chloride/Bromide)  | 
  |
| 
   7  | 
  
   HCl/HBr
  with alkene  | 
  
   Addition via Markovnikov’s rule (Alkene to
  Alkyl Chloride/ Bromide).  | 
  
   | 
 
| 
   8  | 
  
   NaI/KI in
  dry acetone  | 
  
   Substitution of halogens by –I group (Alkyl
  halides to Alkyl Iodide)  | 
  |
| 
   9  | 
  
   NaNO2
  + HCl / HNO2  | 
  
   1° Amine to diazonium salt  | 
  |
| 
   10  | 
  
   Aq.
  KOH/NaOH  | 
  
   Substitution by –OH group (Alkyl halide to
  Alcohol)  | 
  |
| 
   11  | 
  
   Ethanolic
  KCN/ NaCN  | 
  
   Substitution by –CN (Alkyl halide to Alkyl
  Cyanide)  | 
  |
| 
   12  | 
  
   Cl2/Br2
  in Dark or CCl4  | 
  
   Alkene to vicinal dichloride / dibromide  | 
  |
| 
   13  | 
  
   AgCN  | 
  
   Substitution by –NC (isocyanide) group
  (Alkylhalide to Alkyl isocyanide)  | 
  |
| 
   14  | 
  
   KNO2  | 
  
   Substitution by –ONO (Alkyl halide to
  Alkylnitrile)  | 
  |
| 
   15  | 
  
   AgNO2  | 
  
   Substitution by –NO2 (Alkyl
  halide to Nitroalkane)  | 
  |
| 
   16  | 
  
   Alcoholic
  KOH/ NaOH  | 
  
   β-elimination reaction (Alkyl halide to
  alkene)  | 
  |
| 
   17  | 
  
   Cl2,
  Anhydrous AlCl3  | 
  
   Chlorination of aromatic compounds  | 
  |
| 
   18  | 
  
   Conc. HNO3
  + Conc. H2SO4  | 
  
   Nitration of aromatic compounds  | 
  |
| 
   19  | 
  
   Conc. H2SO4  | 
  
   Sulphonation of aromatic compounds  | 
  |
| 
   20  | 
  
   CH3Cl
  + Anhydrous AlCl3  | 
  
   Methylation (alkylation) of aromatic
  compounds (Friedel Craft alkylation).  | 
  |
| 
   21  | 
  
   CH3COCl
  + Anhydrous AlCl3  | 
  
   Ethanoylation (acylation) of aromatic
  compounds (Friedel Craft acylation).  | 
  |
| 
   22  | 
  
   H2O,
  H+  | 
  
   Hydration of alkene to alcohol  | 
  |
| 
   23  | 
  
   H2,
  Ni/Pt/Pd  | 
  
   Hydrogenation of alkene to Alkane,
  Reduction of Aldehyde to alcohol etc.   | 
  |
| 
   24  | 
  
   NaBH4  | 
  
   Mild reducing agent, Ketone to alcohol.  | 
  |
| 
   25  | 
  
   LiAlH4/
  B2H6  | 
  
   Strong reducing agent, Carboxylic acid to
  Alcohol.  | 
  |
| 
   26  | 
  
   RMgX
  (Grignard Reagent)  | 
  
   Aldehydes and ketones to alcohols  | 
  |
| 
   27  | 
  
   Conc. H2SO4  | 
  
   Dehydration (Alcohols to alkene)  | 
  |
| 
   28  | 
  
   Acidified
  KMnO4 /Alkaline KMnO4/Acidified K2CrO7/
  CrO3-H2SO4 (Jones reagent)  | 
  
   Strong oxidizing agent (Alcohols to
  Carboxylic acid)  | 
  |
| 
   29  | 
  
   CrO3/PCC  | 
  
   Mild oxidizing agent (Alcohols to aldehyde
  or ketone)  | 
  |
| 
   30  | 
  
   DIBAL-H  | 
  
   Strong reducing agent. (Cyanide to aldehyde, Ester to Aldehyde)  | 
  |
| 
   31  | 
  
   Br2
  + NaOH  | 
  
   Hoffmann Bromamide Degradation reaction
  (Amide to Amine).  | 
  |
| 
   32  | 
  
   CHCl3 + 3KOH  | 
  
   Carbylamine reaction (Primary amine to
  Alkyl isocyanide)  | 
  






























Waiting for video explanation......thnkx for providing the soft copy of much easy notes(#of reagents)..will be helpful while revision......
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