The correct statement regarding the basicity of aryl amines is:

Aryl amines are generally less basic than alkyl amines because the nitrogen lone-pair electrons are delocalized by interaction with the aromatic ring π electron system.

Aryl amines are generally more basic than alkyl amines because the nitrogen lone-pair electrons are not delocalized by interaction with the aromatic ring π electron system.

Aryl amines are generally more basic than alkyl amines because of aryl group.

Aryl amines are generally more basic than alkyl amines, because the nitrogen atom in aryl amines is sp-hybridized.

E M B I B E

Beta Question Bank for Medical: Chemistry>Chapter 21 - Organic Chemistry- Some Basic Principles and Techniques>BEGINNER'S BOX>Q 47

EASY

NEET

IMPORTANT

Earn 100

Decreasing order of $- I$ effect of the triad $[- {NO}_{2}, - \overset{\oplus}{N} H_{3}, - CN]$ is:

50% studentsanswered this correctly

Important Questions on Organic Chemistry- Some Basic Principles and Techniques

EASY

NEET

IMPORTANT

Beta Question Bank for Medical: Chemistry>Chapter 21 - Organic Chemistry- Some Basic Principles and Techniques>BEGINNER'S BOX>Q 48

Most stable carbanion is :-

EASY

NEET

IMPORTANT

Beta Question Bank for Medical: Chemistry>Chapter 21 - Organic Chemistry- Some Basic Principles and Techniques>BEGINNER'S BOX>Q 49

The correct order of stability of given carbanions will be:-

$\begin{matrix} {CH}_{3} - \overset{⊝}{C} H_{2} \\ (I) \end{matrix}$ $\begin{matrix} {CH}_{2} = \overset{⊝}{C} H_{2} \\ (II) \end{matrix}$ $\begin{matrix} HC \equiv \overset{⊝}{C} \\ (III) \end{matrix}$