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Reaction involving Carboxyl group (-COOH)

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Question#1

The reagent used for converting ethanoic acid to ethanol is [KCET 1996; EAMCET 1998]

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Question#2

The fatty acid which shows reducing property is [Kerala CET 2000]

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Question#3

\( CH_3-COOH \xrightarrow[\Delta]{P2O5} X \) Identify X [JIPMER 2000; CPMT 2003]

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Question#4

The correct product of complete reduction of propionic acid is ; (2018-ETEA)

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Question#5

Carboxylic acid are rather hard to reduce, which powerful reducing agent can be used to convert them to the corresponding primary alcohol  MDCAT2015

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1.    Introduction To Fundamental
         Atomic Mass
         Empirical formula
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2.    Atomic Strcuture
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         Relation between kp and kc
         Factor effecting balance of chemical equilibrium (Le chatelier's principle)
         Common ion effect
         Ph
         Buffers
         Solubility Product
         Lowry-Bronsted acid base concept
7.    Reaction kinetics
         Rate of reaction
         Velocity constant or rate constant( K)
         rate Laws
         order of reaction
         Zero order reactions
         First order reactions
         Second order Reactions
         Third order reactions
         Half life of reaction
         How to determine rate of reaction.
         Ea(activation energy)
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8.    Thermochemistry
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11.    s and p block Elements
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12.    Transition Elements
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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
         Naming and Designation Of Alcohols
         Physical properties of Alochols
         Preparations of Alcohols
         Reactivity of Alcohols
         Predicting Relative acidity of alcohols
         iodoform test
         Lucas test
         Naming of aromatic hydroxy groups (phenol)
         Physical properties of phenol
         Preparation Of phenols
         Reactions of phenols
         Acidity of Phenols
         Identification test for Phenol
17.    Alkyl halides
         IUPAC system
         Preparations of alkyl halides
         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