Hybridization of nitrogen atom in pyridine is:

The hybridization of nitrogen atom in amines

The hybridization of nitrogen in primary amine is……..

The lone pair of amines makes them basic. They react with acids to form acid-base salts. Amines are more basic than alcohols, ethers and water. When an amine is dissolved in water, an equilibrium is established , where water acts as an acid and transfer a proton to the amine. The basic strength of an amine can be measured by basicity constant K_(b) . Arylamines are less basic than alkylamines because the lone pair of nitrogen is delocalised with the aromatic ring and are less available for donation. Substituted arylamines can be either more basic or less basic than aniline , depending on the substituted . ERG substituents, such as -CH_(3), -NH_(2) and -OCH_(3) increases the basicity and EWG substituents , such as -Cl, -NO_(2) and -CN decreases basicity. While sp^(2)- hybridized nitrogen atom in pyridine is less basic then the sp^(3) -hybridized nitrogen in an alkylamine. The most basic carbanion is :

Correct energy profile for amine inversion and hybridization of nitrogen in transition state is:

Correct energy profile for amine inversion and hybridization of nitrogen in transition state is:

The hybridization states of the nitrogen atom in pyridine piperidine and pyrrole are respectively