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Statement-1: Ethyne is stronger acid tha...

Statement-1: Ethyne is stronger acid than ethene.
and
Statement-2 Introduction of alkyl group activates benzene ring

A

(a) Statement-1 is True , Statement-2 is True , Statement-2 is a correct explanation for Statement-2

B

(b) Statement-1 is True , Statement-2 is True , Statement-2 is NOT a correct explanation for Statement-2

C

(c) Statement-1 is True , Statement-2 is False

D

(d) Statement-1 is False , Statement-2 is True

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to analyze both statements provided in the question. ### Step 1: Analyze Statement 1 **Statement 1:** Ethyne is a stronger acid than ethene. - **Understanding Acidity:** The acidity of a compound is determined by its ability to donate protons (H⁺). When a compound donates a proton, it forms a conjugate base. - **Structures of Ethyne and Ethene:** - Ethyne (C₂H₂) has the structure H-C≡C-H (triple bond). - Ethene (C₂H₄) has the structure H₂C=CH₂ (double bond). - **Hybridization:** - In ethyne, the carbon atoms are sp hybridized. - In ethene, the carbon atoms are sp² hybridized. - **S-character:** - The sp hybridization has 50% s-character, while sp² has 33% s-character. - Greater s-character means greater electronegativity, which stabilizes the negative charge on the conjugate base. - **Conclusion for Statement 1:** Since the conjugate base of ethyne is more stable due to higher s-character, ethyne is indeed a stronger acid than ethene. Therefore, **Statement 1 is true.** ### Step 2: Analyze Statement 2 **Statement 2:** Introduction of alkyl group activates the benzene ring. - **Understanding Activation of Benzene:** - Alkyl groups are electron-donating groups and can activate the benzene ring towards electrophilic substitution. - **Mechanism of Activation:** - The alkyl group can stabilize the positive charge that develops during the reaction through hyperconjugation and resonance. - **Example:** - If a methyl group (–CH₃) is attached to benzene, it can donate electron density to the ring, making it more reactive. - **Conclusion for Statement 2:** The introduction of an alkyl group does activate the benzene ring through hyperconjugation. Therefore, **Statement 2 is also true.** ### Step 3: Determine Relationship Between Statements - **Are the statements related?** - Statement 1 discusses acidity, while Statement 2 discusses the activation of the benzene ring. They are both true but refer to different concepts. - **Correct Explanation:** Statement 2 does not explain Statement 1, as they pertain to different chemical properties. ### Final Conclusion - **Option B is correct:** Statement 1 is true, Statement 2 is true, but Statement 2 is not a correct explanation for Statement 1.
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