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HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

Which of the following substances has the least covalent character?

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

Which of the following compounds have the same no. of lone pairs with their central atom? (I) XeF (II) BrF (III) XeF (IV) H S (V) Triple Methylene

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

The dipole moment of o, p and m-dichlorobenzene will be in the order :

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

Which has a maximum dipole moment? (a) (b) (c) (d)

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

Which molecule has regular geometry? (I) SnCl (II) NH (III) PCl (IV) SF

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryChemical Bonding

Which molecular geometry is least likely to result from a trigonal bipyramidal electron geometry?

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Ethyl isocyanide on hydrolysis in acidic medium generates

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The end product B in the sequence of reactions, Carboxylic Acid and Its Derivatives CN NaOH R X A B → → is

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Here Z is (a)

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

When propionic acid is treated with aqueous sodium bicarbonate, CO₂ is liberated. The C of CO₂ comes from

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

When CH₂ = CH – COOH is reduced with LiAlH , the compound obtained will be:

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

End product of the following reaction is Cl alc. KOH red p CH CH COOH A B → → (a) (b) (c) (d)

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which of the following is correct order of acidity?

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The correct order of increasing acid strength of the compounds

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In a set of the given reactions, acetic acid yielded a product C. O C H (i) C H MgBr Anh.AlCl (ii) H CH COOH PCl A B C → → → Product C would be (a)

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Which of the following represents the correct order of the acidity in the given compounds?

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

The correct order for the acidic character of the following carboxylic acids is

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Hydrogenation of benzoyl chloride in the presence of Pd-BaSO₄ gives

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Ethyl Acetate O (i)CH MgBr (excess) (ii) H → P, the product will be (a) (b) (c) (d)

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Benzoyl chloride is prepared from benzoic acid by

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In the following sequence of reactions: KMnO SOCl H /Pd BaSO Toluene A B C, → → → Carboxylic Acid and Its Derivatives the product C formed will be :

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Acetamide is treated separately with the following reagents. Which one of these would give methyl amine?

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Benzamide on treatment with POCl₃ gives

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

In the given reaction, H O C H CO O I → H O C H COOCOCH II → Identify the product(s) formed in the given reaction. I II

HARDMCQ SINGLEJEE Mains ChemistryInorganic ChemistryCarboxylic Acids and Derivatives

Assertion : p–hydroxybenzoic acid has a lower boiling point than o–hydroxybenzoic acid. Reason : o–hydroxybenzoic acid has intramolecular hydrogen bonding.

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