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Assertion. Acidity of the C-H bond decre...

Assertion. Acidity of the C-H bond decreases in the order: `HC-=CH gt H_2C =CH_2 gt CH_3 -CH_3`
Reason. Acidity of the C-H bond increases as the electronegativity of the carbon to which it is attached increases

A

If both assertion and reason are true, and reason is the true explanation of the assertion.

B

If both assertion and reason are true, but reason is not the true explanation of the assertion.

C

If assertion is true, but reason is false.

D

If both assertion and reason are false

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The correct Answer is:
To solve the question regarding the acidity of C-H bonds in different hydrocarbons, we will analyze the assertion and the reason provided. ### Step-by-Step Solution: 1. **Understanding Acidity in Hydrocarbons**: - Acidity in hydrocarbons is determined by the stability of the conjugate base formed when a hydrogen atom is removed (deprotonation). The more stable the conjugate base, the stronger the acid. 2. **Identifying the Hydrocarbons**: - We have three hydrocarbons to compare: - **HC≡CH** (ethyne or acetylene) - **H₂C=CH₂** (ethylene) - **CH₃-CH₃** (ethane) 3. **Determining the Conjugate Bases**: - When we remove a hydrogen atom from each hydrocarbon, we form the following conjugate bases: - From HC≡CH: HC≡C⁻ - From H₂C=CH₂: H₂C=CH⁻ - From CH₃-CH₃: CH₃-CH₂⁻ 4. **Analyzing Hybridization**: - The hybridization of the carbon atoms in these hydrocarbons affects the acidity: - HC≡CH: sp hybridized (50% s character) - H₂C=CH₂: sp² hybridized (33% s character) - CH₃-CH₃: sp³ hybridized (25% s character) 5. **Understanding s Character and Acidity**: - Higher s character in hybridized orbitals means that the electrons are held closer to the nucleus, which stabilizes the negative charge on the conjugate base. - Therefore, the order of acidity based on hybridization is: - HC≡CH > H₂C=CH₂ > CH₃-CH₃ 6. **Conclusion on Assertion**: - The assertion that the acidity of the C-H bond decreases in the order: HC≡CH > H₂C=CH₂ > CH₃-CH₃ is correct. 7. **Evaluating the Reason**: - The reason states that the acidity of the C-H bond increases as the electronegativity of the carbon to which it is attached increases. - This is true because higher electronegativity means a greater ability to stabilize the negative charge on the conjugate base. 8. **Final Conclusion**: - Both the assertion and the reason are correct, and the reason correctly explains the assertion. ### Final Answer: - The assertion is correct, and the reason is also correct. The correct answer is option (1).
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