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MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Select the incorrect match.

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The product formed during Hell-Volhard-Zelinsky reaction is (a) R CH COOH | X (b) R CH COX (c) X | R C COOH | X (d) R CH CH COOH | X

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Diborane easily reduce the functional group such as

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Direct attachment of groups such as phenyl or vinyl to the carboxylic acid, increases the acidity of corresponding carboxylic acid because

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetyl chloride cannot be obtained by treating acetic acid with

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which will not give acetamide on reaction with ammonia

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetic anhydride is obtained from acetyl chloride by the reaction of

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The reaction, H orOH RCOOR R OH excess RCOOR R OH -> is called

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The reaction, CH3COOH + CH3OH → CH3COOCH3 + H2O is called

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

(a) (b) (c) (d)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Above ester has chiral carbon (*). Alkaline hydrolysis gives an acid salt and an alcohol. Select correct statement about alcohol.

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

A is (a) (b)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

LiAlH H O C H COO CH C H CH OH CH OH ->

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In the Hofmann bromamide degradation reaction, the number of moles of NaOH and Br2 used per mole of amine produced are :

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Phenol can be distinguished from acetic acid by

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Tollen’s reagent in not reduced by

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which one of the following compounds forms a red coloured solution on treatment with neutral FeCl3solution

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Ethyl acetate is obtained when methyl magnesium bromide reacts with (Manipal 2008)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Propionic acid with Br2/P yields a dibromo product the structure would be (CBSE AIPMT 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Here, the compound X can be (AFMC 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The correct set of reagents for the following conversion is: (AIIMS 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Identify ‘Z’ in the following sequence of reactions. NH P O CH COOH X Y Z -> -> -> (CPMT 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The acidic nature of carboxylic acids RCOOH RCOO H -> is due to (Manipal 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

When propionic acid is treated with aqueous sodium bicarbonate, CO2 is liberated. The ‘C’ of CO2 comes from (Manipal 2009)

MEDIUMMCQ SINGLENEET ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In the following reaction, Conc. H SO H O C H OH CH COOH CH COOC H -> C2H5OH acts as (AFMC 2009)

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