Chemistry IIT JEE Mains Study Material for Nitro Compounds
Nitro Compounds: IIT JEE Mains Study Material

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Chemistry IIT JEE Mains Study Material for Nitro Compounds Theory Notes includes Alkyl Amine : ,Methods of Preparation : ,From Alkanamide : ,From Alkylchloride : ,By reduction of Nitro compounds : ,From Alcohol : ,From Grignard reagent : ,From Alkyl isocyanate (Alkaline Hydrolysis) : ,From Alkanoic acid (Schimdt Reaction ); ,By Alkyl cyanide (By reaction) : ,From Aldoxime (By Reduction) : ,From Acyl halide : ,From Acyl halide : ,From Phthalic acid : ,By Aldehyde or ketone (reaction wtih H2 and NH3 in presence of catalyst) : ,By reaction of aldehyde or ketones (with ammonium formate or with formamide and subsequent hydrolysis of product) : ,Physical Properties : ,Chemical Properties : ,Chemical Reaction : ,Salt Formation : ,Reaction with water : ,Reaction with HNO2 : ,Isocyanide test or Carbylamine reaction : ,Acylation : ,Alkylation : ,Oxidation : ,Reaction with Aldehydes and Ketone : ,Mustard oil reaction : ,Reaction with Grignard reagent : ,Reaction with Hinsberg reagent : ,Reaction with Nitrosyl chloride (TILDEN’S REAGNET) : ,Reaction with HAuCl4 (Chloroauric Acid) and H2 PtCl6 (Chloroplatinic Acid) : ,Reaction with Caro’s acids [H2SO5] : ,Seperation of Mixtures of Amines : ,Fractional distillation : ,Hofmann method : ,Hinsberg method : ,Cyanides, Isocyanides, Alkyl Nitrites and Nitro Alkanes : ,Introduction : ,Alkyl cyanides : ,Methods of Preparation : ,Physical properties : ,Chemical properties :[i] Hydrolysis : Alkyl cyanides ,Alkyl isocyanides : ,Methods of Preparation : ,Physical Properties : ,Chemical Properties : ,Distinction between Ethyl Cyanide and Ethyl Isocyanide : ,Alkyl nitriltes and nitro alkanes : ,Ethyl nitrite C2H5O–N=O : ,Properties : ,Nitro alkanes : ,Physical properties : ,Chemical properties : ,Uses : ,Introduction : ,Method of Preparation : ,Extraction from Urine : ,Wohler’s method : ,From Phosgene gas : ,From Ethyl carbonate : ,From Ethyl carbonate or urethane : ,Hydrolysis of Cyanamide : ,2N–CN + H2O NH2CONH2, Physical Properties : ,Chemical Reactions : ,Effect of heat : ,Salt Formation : ,Reaction with Nitrous acid : ,Reaction with Hypobromite solution : ,Reaction with Hydrazine (NH2–NH2) : ,Reaction with SOCl2 : ,Reaction with fuming H2SO4 : ,Reaction with oxalic ester : ,Reaction with Acetoacetic ester : ,Reaction with NaOCl : ,Methods of Preparation : ,From Benzene (Nitration) : ,Physical Properties : ,Resonance in nitrobenzene : ,Chemical Reactions : ,Reaction of –NO2 group : ,Readuction : ,Reaction with AlCl3 : ,Reaction of Benzene ring : ,Halogenation : ,Sulphonation : ,Other Reactions : ,Reaction with Solid KOH : ,Reaction with Sodamide : ,Reaction with Ethanol : ,Test for Nitrobenzene : ,Method of Preparation : ,From Benzamide : ,From Chlorobenzene : ,From Phenol : ,From phenyl isocyanate (By alkaline hydrolysis) : ,By reudction of azo and hydrazo compounds with sodium dithionite : ,By curtius reaction : ,By Gabriel Phthalimide reaction : ,Physical properties : ,Resonance in Aniline : ,Schotten–baumann reaction : ,Reaction with Hinsberg reagent : ,Reaction with Phosgene : ,Reaction with Carbondisulphide : ,Reaction with Grignard reagent : ,Reaction with HNO2 and HCl (Diazotisation) : ,Reaction with Sodium metal : ,Salt formation ,Reaction with Benzaldehyde : ,Reaction of benzene ring : ,Halogenation : ,
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