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Statement-I: Tert-Butoxide is a stronger...

Statement-I: Tert-Butoxide is a stronger base than `OH^(-)` or `C_(2)H_(5)O^(-)` ion but is a much poorer nucleophile
Because
Statement-II: A negatively charged ions is always more powerful nucleophile than its conjugate acid.

A

Statement-I is True, Statement-II is True : Statement-II is a correct explanation for Statement-I

B

Statement-I is True, Statement-II is True : Statement-II is `NOT` a correct explanation for Statement-I

C

Statement-I is True, Statement-II is False.

D

Statement-I is False, Statement-II is True.

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AI Generated Solution

The correct Answer is:
To analyze the given statements, we will break down the reasoning behind each statement step by step. ### Step 1: Understanding Statement-I **Statement-I:** Tert-Butoxide is a stronger base than OH⁻ or C₂H₅O⁻ but is a much poorer nucleophile. 1. **Structure of Tert-Butoxide:** Tert-butoxide (t-BuO⁻) has the structure (CH₃)₃CO⁻. It has three methyl groups attached to the oxygen. 2. **Basicity:** The presence of three electron-donating methyl groups increases the electron density on the oxygen atom, making t-BuO⁻ a stronger base compared to OH⁻ (hydroxide) and C₂H₅O⁻ (ethoxide). The +I effect from the alkyl groups enhances its basicity. 3. **Nucleophilicity:** Despite being a strong base, t-BuO⁻ is a poor nucleophile. This is due to steric hindrance caused by the bulky tert-butyl group, which makes it difficult for the nucleophile to approach and attack electrophilic centers. ### Step 2: Understanding Statement-II **Statement-II:** A negatively charged ion is always a more powerful nucleophile than its conjugate acid. 1. **Conjugate Acids and Bases:** For any acid-base pair, the conjugate acid is formed by adding a proton (H⁺) to the base. For example, the conjugate acid of OH⁻ is H₂O, and the conjugate acid of C₂H₅O⁻ is C₂H₅OH. 2. **Nucleophilicity Comparison:** Negatively charged ions (like OH⁻ or C₂H₅O⁻) have a complete negative charge and are generally better nucleophiles than their corresponding neutral conjugate acids (like H₂O or C₂H₅OH). This is because the negative charge increases the electron density, making it more reactive towards electrophiles. ### Conclusion - **Statement-I is True:** Tert-butoxide is indeed a stronger base than hydroxide or ethoxide but is a poorer nucleophile due to steric hindrance. - **Statement-II is True:** A negatively charged ion is generally a more powerful nucleophile than its conjugate acid because of the presence of a complete negative charge. ### Final Answer Both statements are true, but Statement-II does not explain Statement-I. Therefore, the answer is: **Option B:** Statement I is true, Statement II is true, but Statement II is not the correct explanation for Statement I. ---
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ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-3
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  4. Assertion : Phenol forms 2, 4, 6-tribromophenol on treatment with Br2 ...

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  5. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  6. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  7. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  8. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  9. Phenols are converted into their salts by aqueous NaOH but not by aque...

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  10. Symmetrically subsituted epoxides give the same products in both the a...

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  11. Symmetrically subsituted epoxides give the same products in both the a...

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  12. Symmetrically subsituted epoxides give the same products in both the a...

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  13. Symmetrically subsituted epoxides give the same products in both the a...

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  14. Symmetrically subsituted epoxides give the same products in both the a...

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  15. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  16. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  17. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  18. What will be the product of following reaction S is:

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  19. When pinacol is treated with dilute H(2)SO(4), a re-arangement reactio...

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  20. The yield of ketone is oxidised is more than the yield of aldeyde whe...

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