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MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetyl chloride cannot be obtained by treating acetic acid with

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

An alkyl cyanide forms an amide when it is treated with

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Two moles of acetic acid are heated with P2O5, The product formed is

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Heating a mixture of ethyl alcohol and acetic acid in presence of conc. H2SO4 produces a fruity smelling compound. This reaction is called

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which reagent will bring about the conversion of carboxylic acids into esters

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In esterification, OH ion for making H2O comes from:

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The product D of the reaction is

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Reagents I and II given in the reactions are:

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Maximum keto-enol tautomerism is shown by

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The decreasing order of reactivity of (i) CH3COCl (ii) CH3COOC2H5 (iii) CH3CONH2 (iv) (CH3CO)2O Towards nucleophilic acyl substitution is

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

H Pd/BaSO CH COCl CH CHO HCl; -> The above reaction is called

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

O O || || CH C Cl Nu CH C Nu Cl -> Reactivity order of different nucleophiles (NH2-, CH3COO-, OH-) is in order

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Benzoyl chloride on treatment with ammonia gives

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetic anhydride reacts with excess of ammonia to form

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which will not give acetamide on reaction with ammonia

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetic anhydride is obtained from acetyl chloride by the reaction of

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

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

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

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

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

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

MEDIUMMCQ SINGLEJEE Advanced 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 SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

A is (a) (b)

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

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

MEDIUMMCQ SINGLEJEE Advanced 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 SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Phenol can be distinguished from acetic acid by

MEDIUMMCQ SINGLEJEE Advanced ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Tollen’s reagent in not reduced by

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