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SUMMARY OF Unit 12: Aldehyde, Ketones and Carboxylic-PART1Introduction:Organic compounds containing carbon-oxygen double bond (>C=O) called carbonyl group.
Nomenclature of Aldehyde & Ketone Nomenclature of Carboxylic acids Structure of functionalgroups:Structure Of carbonylfunctional group:
Structure Of –COOHfunctional group:
Preparation of aldehydes & Ketones: Preparation of Aldehydes Preparation of CarboxylicAcids:
1.By oxidation of alcohols:
2. By dehydrogenation of Alcohols:
3.By ozonolysis of Alkenes:>C=C< +O3/ Zn+H2O >C=O +O=C<
4.By hydration of alkynes:
1.From acyl chloride - Rosenmundreduction:
2. From nitriles (StephenReaction)
3. From hydrocarbonsi. By oxidation of methylbenzene-a. use of chromylchloride(CrO2Cl2)
b. use of chromic oxide(CrO3)
(ii) By side chain chlorinationfollowed by hydrolysis:
(iii) By Gatterman- Koch reaction:
1.From primary alcoholsand aldehydes-
2.From alkylbenzenes byoxidation:
3. From nitriles and amides
4. From Grignard reagents
5. From acyl halides andanhydrides
6. From estersPreparation of Ketones:1.From acyl chlorides:
2.From nitriles:
3. Friedel-Crafts acylation reaction:
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SUMMARY OF Unit 12: Aldehyde, Ketones and Carboxylic-PART2
Chemical Reactions of aldehydes& ketones
Chemical Reactions of aldehydes& ketones
Chemical Reactions of carboxylicacid
Nucleophilic addition reactions:
(a)Addition of hydrogen cyanide(HCN):Formation ofCyanohydrin
(b) Sodium hydrogensulphiteadds to aldehydes and ketones toform the addition products
(c) Addition of alcohols:
Ketones react with ethyleneglycol to form cyclic productsknown as ethylene glycol ketals.
(d) Addition of Grignardreagents:
(d) Addition of ammonia and itsderivatives:
2.Reduction:(i) Reduction to alcohols:
(ii) Reduction to hydrocarbons:a. Clemmensen reduction
b. Wolff-Kishner reduction
3. Oxidation: by (i)KMnO4/Acidic(ii) K2CrO7/Acidic
Oxidation by mild oxidizingagent-Tollens’ test:
Oxidation by mild oxidizingagent-Fehling’s test:
(iii)Oxidation of methyl ketone byhaloform reaction:
4.Reactions due to δ–hydrogen:(i)Aldol Condensation:
(ii)Cross aldol Condensation:
1.Reaction involving Cleavage ofO-H bond, Acidity of Caboxylicacid :Carboxylic acids dissociate togive resonance stablisedcarboxylate anions & hydroniumion-
The presence of electronwithdrawing group on the phenyl ofaromatic carboxylic acid increasestheir acidity while electrondonating groups decrease theiracidity.
2.Reaction involving Cleavage ofO-H bond:i.Formation of anhydride:
ii.Esterification:
iii.Reaction with PCl3, PCl5 ,SOCl2 :
iv.Reaction with ammonia:
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5.Other reactions:(i)Cannizaro reaction:
(ii)Electrophilic substitutionreaction:
3.Reactions Involving –COOHGroup:i.Reduction:
ii.Decarboxylation:
4.Substitution Reaction in theHydrocarbon Part:i.Halogenation, Hell –Vohlord –Zelensky reaction:
ii.Ring substitution:
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