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Home/Aldehyde and ketones

oxidation reduction Reactions of carbonyls

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Question#1

The reagent with which both aldehyde and acetone react easily is[CPMT 1973, 74

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Question#2

Which one of the following on oxidation will not give a carboxylic acid with the same number of carbon atoms [CBSE PMT 1992; MP PET 1996]

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Question#3

Reduction of an aldehyde produces [MP PMT 1994; MP PET 2001]

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Question#4

Reduction of Aldehydes and Ketones to hydrocarbon take place in the presence of [CPMT 2003]

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Question#5

Methyl phenyl ketone can be converted  into ethyl benzene in one step by using NUMS2016

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1.    Introduction To Fundamental
         Atomic Mass
         Empirical formula
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         Common ion effect
         Ph
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         Solubility Product
         Lowry-Bronsted acid base concept
7.    Reaction kinetics
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         Velocity constant or rate constant( K)
         rate Laws
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         Third order reactions
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11.    s and p block Elements
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         Reactions of group 1 elements( Alkali metals)
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12.    Transition Elements
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13.    Fundamental Concepts of Organic Chemistry
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         Classification of organic compounds based on carbon skeleton
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14.    Chemistry Of Hydrocarbons
         Introduction
         IUPAC Naming
         Physical Properties of Alkane Alkene and Alkynes
         Preparations Of Alkanes
         Preparation of alkenes
         Preparations Of alkynes
         Reactivity Of Alkanes
         Reactivity Of alkene
         Reaction Of Alkyne
         Acidity Of terminal Alkynes
         Reactivity comparison of Hydrocarbons
15.    Benzene
         IUPAC Naming and classification
         Physical properties of benzene
         Molecular orbital Aspects
         Resonance energy and Stability of benzene
         Preparation of benzene
         Reactivity and reactions ( catalytic Hydrogenation, Oxidation, Nitration, Halogenation, Sulphonation )
         Fridel Craft Alkylation and Acylation
         Substituent effects
16.    Alcohol and phenols
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         iodoform test
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         Physical properties of phenol
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         Reactions of phenols
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17.    Alkyl halides
         IUPAC system
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         Reactivity of Alkyl halides
         SN1 & SN2
         E1 & E2
         Nucleophile and Base
         Substrate and Leaving group
         Organomettalic Compound (Grignard Reagent)
18.    Aldehyde and ketones
         Nomenclature and structure of Aldehyde and ketones
         preparation of Ald & Ket
         Relative Reactivity of carbonyls
         Addition Of HCN and NaHSO3 to Carbonyls
         Aldol condensation
         Cannizaro's reaction
         Addition Elimination reactions
         oxidation reduction Reactions of carbonyls
         Identifications Reactions
19.    Carboxylic acid
         Nomenclature
         Physical properties
         Preparation of carboxylic acid by ( carbonation of Grignard reagent, Hydrolysis of Nitriles, oxidation of alcohols and aldehydes , oxidative cleavage of Alkene,
         Reaction involving H-atom of the carboxylic acid
         Reaction involving the OH-group of carboxylic acid
         Reaction involving Carboxyl group (-COOH)
         Acidity
         Tests for carboxylic Group
         Preparation and Reactions of carboxylic acid derivatives
20.    Macromolecules