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picture1_Namma Kalvi 12th Chemistry Unit 12 Ppt Material Em 218450


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File: Namma Kalvi 12th Chemistry Unit 12 Ppt Material Em 218450
unit no 12 carbonyl compounds and carboxylic acids introduction nomenclature of aldehydes and ketones structure of carbonyl group general method preparation of aldehydes and ketones i ozonolysis of alkenes ii ...

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        UNIT NO.12.CARBONYL COMPOUNDS 
        AND CARBOXYLIC ACIDS
          INTRODUCTION
          NOMENCLATURE OF ALDEHYDES AND 
            KETONES
          STRUCTURE OF CARBONYL GROUP
          GENERAL METHOD PREPARATION OF 
            ALDEHYDES AND KETONES
        (i)Ozonolysis of alkenes (ii) Hydration of 
       alkynes (iii) From calcium salts of carboxylic 
       acids- Aldehydes and symmetrical ketones
                                                                R.ABDUL SALEEM,P.G.T.CHEM.TR.  09/09/2022                  2
        ALDEHYDES & KETONES
           PREPARATION OF ALDEHYDES- 
             (a)Rosenmund Reduction (b)Stephen’s 
             reaction ©Slective reduction cyanides
           PREPARATION OF BENZALDEHYDE: (i)Side 
             chain oxidation of toluene and its 
             derivatives (ii)Gattermann-Koch reaction 
             (iii)Manufacture of benzaldehyde from 
             toluene.
           PREPARATION OF KETONES: (a)By dialkyl 
             Cadmium (b)Friedal crafts acylation.
                                                                R.ABDUL SALEEM,P.G.T.CHEM.TR.  09/09/2022                  3
        PROPERTIES OF ALDEHYDES & 
        KETONES
           PHYSICAL PROPERTIES OF ALDEHYDES AND KETONES
           CHEMICAL PROPERTIES OF ALDEHYDES AND KETONES: 
             Nucleophilic addition reaction – (a)Addition of HCN 
             (b)Addition of NaHSO3 ©Addition of Alcohol 
             (d)Addition of ammonia and its derivatives- 
             (i)Hydroxylamine (ii)Hydrazine (iii)Phenyl Hydrazine. 
             (e)Reaction with Ammonia, Properties  structure and 
             uses
           OXIDATION OF ALDEHYDES AND KETONES:
           REDUCTION REACTIONS : (a) Aldehyde reduced to 
             primary alcohols, (b) ketone reduced to Secondary 
             alcohols ( C ) Reduction tHydrocarbons , 
             (d)Clemmensen reduction (e)WolfKishner reduction 
             (f)Reduction to Pinnacols 
           HALOFORM REACTION.
                                                                R.ABDUL SALEEM,P.G.T.CHEM.TR.  09/09/2022                  4
        ALDEHYDES & KETONES
          REACTION INVOLVING ALKYL GROUP
         (1)ALDOL CONDENSATION, AND 
        MECHANISM
         (2)CROSSED ALDOL CONDENSATION
         (3)CLAISEN-SCHMIDT CONDENSATION
         (4)CANNIZARO REACTION, & 
        MECHANISM
         (5)CROSSED CANNIZARO REACTION
         
                                                                R.ABDUL SALEEM,P.G.T.CHEM.TR.  09/09/2022                  5
        ALDEHYDES & KETONES
          (6) BENZOIN CONDENSATION
          (7) PERKIN’S REACTION
          (8) KNOEVENAGAL REACTION
          (9) REACTION WITH AMINE
          (10)CONDENSATION WITH TERTIARY AROMATIC AMINES
          (11)ELECTROPHILIC SUSBSITUTIONS REACTIONS OF 
            BENZALDEHYDE
          (12)ELECTROPHILIC SUBSTITUTION REACTION OF 
            ACETOPHENONE
          TEST FOR ALDEHYDES:(a)Tollens Reagent Test (b)Fehlings 
            solution Test (3)Benedict’s solution test (4)Schiff’s Reagent Test.
          USES OF ALDEHYDES AND KETONES: (a)Formaldehyde 
            (b)Acetaldehyde ©Acetone (d)Benzaldehyde (e) Aromatic 
            ketones.
                                                                R.ABDUL SALEEM,P.G.T.CHEM.TR.  09/09/2022                  6
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...Unit no carbonyl compounds and carboxylic acids introduction nomenclature of aldehydes ketones structure group general method preparation i ozonolysis alkenes ii hydration alkynes iii from calcium salts symmetrical r abdul saleem p g t chem tr a rosenmund reduction b stephen s reaction slective cyanides benzaldehyde side chain oxidation toluene its derivatives gattermann koch manufacture by dialkyl cadmium friedal crafts acylation properties physical chemical nucleophilic addition hcn nahso alcohol d ammonia hydroxylamine hydrazine phenyl e with uses reactions aldehyde reduced to primary alcohols ketone secondary c thydrocarbons clemmensen wolfkishner f pinnacols haloform involving alkyl aldol condensation mechanism crossed claisen schmidt cannizaro benzoin perkin knoevenagal amine tertiary aromatic amines electrophilic susbsitutions substitution acetophenone test for tollens reagent fehlings solution benedict schiff formaldehyde acetaldehyde acetone...

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