A: Pyrrole is less basic than pyridine.
R: Lone pair electron of nitrogen in pyrrole participate in conjugation to gain aromatic character.

Pyridine is less basic than triethylamine because :

Statement-1: And Statement-2: Lone pair electrons on nitrogen in compound (I) does not participate in resonance.

A: Phthalimide is less basic than acetamide. R: Acetamide is more basic than ethyl amine.

Assertion: Ammonia acts as a ligand. Reason : A lone pair of electrons on nitrogen can be donated to acceptor.

The origin of acidity and basicity in organic compound is great interest and provides an extensive comparison. Among hydrocarbons % a character is taken in aC Count while to decide the acidity, in simple aliphatic acids, more the number of alkyl groups, (+1 effect) less is the acidity & more the (-1 effect) groups larger the acidity and vice-versa in the case of simple alphatic bases. Benzoic acid is more stronger than carboxylic acid as benzoate ion is stablised more by resonance. Aromatic amines are less basic than apiphatic amine as the electron pair is less available in case of aromatic amines. The presence of solvent also plays a very important role and at time governs the order too. Amongst the following the most basic compound is -

The origin of acidity and basicity in organic compound is great interest and provides an extensive comparison. Among hydrocarbons % a character is taken in aC Count while to decide the acidity, in simple aliphatic acids, more the number of alkyl groups, (+1 effect) less is the acidity & more the (-1 effect) groups larger the acidity and vice-versa in the case of simple alphatic bases. Benzoic acid is more stronger than carboxylic acid as benzoate ion is stablised more by resonance. Aromatic amines are less basic than apiphatic amine as the electron pair is less available in case of aromatic amines. The presence of solvent also plays a very important role and at time governs the order too. Which of the following is most acidic

The number of lone pairs of electrons in the nitrogen atom in ammonia molecule is?

Assertion : In strongly acidic solution, aniline becomes less reactive towards electrophilic reagents . Reason : Due to protonation of amino group the lone pair of electrons on nitrogen is not available for donation to benzene ring by resonance .

A : Acetate ion is less basic than the methoxide ion. R : The acetate ion is resonance stabilized.

The origin of acidity and basicity in organic compound is great interest and provides an extensive comparison. Among hydrocarbons % a character is taken in aC Count while to decide the acidity, in simple aliphatic acids, more the number of alkyl groups, (+1 effect) less is the acidity & more the (-1 effect) groups larger the acidity and vice-versa in the case of simple alphatic bases. Benzoic acid is more stronger than carboxylic acid as benzoate ion is stablised more by resonance. Aromatic amines are less basic than apiphatic amine as the electron pair is less available in case of aromatic amines. The presence of solvent also plays a very important role and at time governs the order too. In the following compounds, the oreder of basicity