Home
Class 12
CHEMISTRY
A: Due to ortho effect basic nature of a...

A: Due to ortho effect basic nature of aniline decreases.
R: It is due to steric hinderance because of solvation of cation.

A

If both Assertion & Reason are true and the reason is the correct explanation of the assertion, then mark (1).

B

If both Assertion & Reason are true but the reason is not the correct explanation of the assertion, then mark (2)

C

If Assertion is true statement but Reason is false, then mark (3)

D

If both Assertion and Reason are false statements, then mark (4)

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to analyze the assertion and reason provided regarding the basic nature of aniline and the ortho effect. Here’s a step-by-step breakdown of the solution: ### Step 1: Understanding the Assertion The assertion states that "due to ortho effect, the basic nature of aniline decreases." - **Explanation**: Aniline, which is an aromatic amine, has a lone pair of electrons on the nitrogen atom. This lone pair can participate in protonation, which is a measure of basicity. However, when there are substituents at the ortho position, they can interfere with this process. **Hint**: Consider how substituents on the benzene ring can affect the availability of the lone pair on nitrogen. ### Step 2: Understanding the Reason The reason states that "it is due to steric hindrance because of the solvation of cation." - **Explanation**: The ortho substituents can create steric hindrance, making it difficult for the nitrogen to effectively bond with protons. Additionally, when the aniline is protonated, the resulting cation can be sterically hindered by the ortho substituents, further decreasing the basicity. **Hint**: Think about how the spatial arrangement of atoms can affect chemical interactions, especially in protonation. ### Step 3: Analyzing the Relationship Between Assertion and Reason We need to determine if the reason provided correctly explains the assertion. - **Explanation**: The assertion is true as the ortho effect indeed leads to a decrease in the basicity of aniline. The reason is also true because steric hindrance plays a significant role in this decrease. Therefore, the reason does provide a correct explanation for the assertion. **Hint**: Reflect on whether the steric hindrance mentioned in the reason directly relates to the decrease in basicity stated in the assertion. ### Step 4: Conclusion Both the assertion and the reason are true, and the reason correctly explains the assertion. Therefore, the correct answer is that the assertion is true, the reason is true, and the reason is the correct explanation for the assertion. **Final Answer**: The assertion is true, the reason is true, and the reason is the correct explanation for the assertion.
Promotional Banner

Similar Questions

Explore conceptually related problems

A : Ortho - cresol is weaker acidic than meta-cresol . R : It is due to ortho effect .

Assertion : Due to Frenkel defect, density of the crystalline solid decreases. Reason : In Frenkel defect, cation or anion leaves the crystal.

Assertion (A): Due to common ion effect, the solubility of HgI_(2) is expected to be less in an aqueous solution of KI than in water. But HgI_(2) dissolves in an aqueous solution of KI to form a clear solution. Reason (R) : I^(Theta) ions is highly polarisable.

Assertion :- In case of chemical adsorption, (x)/(m) first increase then decrease with temp. Reason :- The intial increase is due to the fact that heat supplied acts as a activation energy. The decrease afterwards is due to the exothermic nature of adsorption at equilibrium.

A: Aniline is not prepared by Gabriel phthalimide synthesis. R: Due to partial double bond character in haloarene because of resonance.

Attenuation of ground waves is due to (a) Diffraction effect (b) Ratio waves induce currents in the ground because of the polarization

Ortho effect is a special type of effect that is shown by d-substituents, but it is not necessarily just a steric effect.This ortho-effect opertes with the benzoic acid.Irrespective of the polar types nearly all o-substitued benzoic acid are stronger than unsubstituted beznoic acid.Benzoic acid is a resonance hybrid and so the carboxyl group is coplanar with the ring.An o-substituent tends to prevent this coplanarity . Ortho effect also opertes in substituted anilines where as ortho substituent has base weakening effect. What is the order of basicily of following compounds ?

Assertion (A) : Ph overset (o+)(N_2) Br^(Θ) couples with N, N -dimethyl aniline (I) but not with 2,6, -dimethyl- N,N -dimethuyl aniline (II) Reason (R ): Due to steric inhibition of resonance , the p-position of (II) is not sufficiently activated fro the coupling reaction.