Aromatic amines are weaker bases than ammonia due to the electron-withdrawing nature of aryl groups. Discrepancies in interpreting Kb values arise from factors like inductive effects, solvation effects, and steric hindrance, influencing the basic strength of amines.

Aliphatic amines are stronger bases than ammonia due to the +I effect of alkyl groups, leading to high electron density on the nitrogen atom. This effect is reflected in their pKb values, which range from 3 to 4.22.

Larger Kb values or smaller pKb values indicate stronger bases. The pKb value of ammonia is 4.75, and aliphatic amines, with a +I effect of alkyl groups, are stronger bases (pKb range: 3 to 4.22). Aromatic amines, with electron-withdrawing aryl ...

Amines react with mineral acids to form ammonium salts, demonstrating their basic nature. The basic character of amines is better understood through their Kb (base dissociation constant) and pKb (negative logarithm of Kb) values.

Amines exhibit basic character by reacting with acids to form salts. Amine salts, soluble in water but insoluble in organic solvents like ether, can be regenerated to the parent amine when treated with a base such as NaOH.