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Compare the basic strength of the follow...

Compare the basic strength of the following compounds:
`underset((I))(C_(2)H_(5)O^(-))" "underset((II))(C_(2)H_(5)^(-))" "underset((III))(C_(2)H_(5)NH^(-))" "underset((IV))(NH_(2^(-)))" "underset((V))(F^(-))`

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To compare the basic strength of the given compounds, we need to consider the concept of basicity in organic chemistry. Basic strength is influenced by the ability of a compound to donate a lone pair of electrons. The more electronegative an atom is, the less likely it is to donate its electrons, which inversely affects basic strength. ### Step-by-Step Solution: 1. **Identify the Compounds**: - (I) \( C_2H_5O^- \) (Ethoxide ion) - (II) \( C_2H_5^- \) (Ethyl anion) - (III) \( C_2H_5NH^- \) (Ethylamine anion) - (IV) \( NH_2^- \) (Amide ion) - (V) \( F^- \) (Fluoride ion) 2. **Understand Electronegativity**: - Electronegativity is the tendency of an atom to attract electrons. The more electronegative an atom, the less likely it is to donate its electrons. - The order of electronegativity for the relevant atoms is: - \( F > O > N > C \) 3. **Analyze Each Compound**: - **(I) Ethoxide ion \( C_2H_5O^- \)**: Oxygen is electronegative, which decreases its basicity compared to carbon-based anions. - **(II) Ethyl anion \( C_2H_5^- \)**: Carbon is less electronegative than oxygen and nitrogen, making this a strong base. - **(III) Ethylamine anion \( C_2H_5NH^- \)**: Nitrogen is less electronegative than oxygen, but more than carbon, so it has moderate basicity. - **(IV) Amide ion \( NH_2^- \)**: Similar to ethylamine, but with no alkyl group to stabilize the negative charge, making it a weaker base than ethylamine. - **(V) Fluoride ion \( F^- \)**: Fluorine is highly electronegative, making this the weakest base among the given compounds. 4. **Rank the Basic Strength**: - Based on the above analysis, we can rank the basic strength from strongest to weakest: 1. \( C_2H_5^- \) (Ethyl anion) - Strongest 2. \( C_2H_5NH^- \) (Ethylamine anion) 3. \( NH_2^- \) (Amide ion) 4. \( C_2H_5O^- \) (Ethoxide ion) 5. \( F^- \) (Fluoride ion) - Weakest ### Final Order of Basic Strength: \[ C_2H_5^- > C_2H_5NH^- > NH_2^- > C_2H_5O^- > F^- \]
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RESONANCE ENGLISH-GENERAL ORGANIC CHEMISTRY II-Exercise-1
  1. Arrange the following in decreasing order of stability

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  2. Arrange the following in decreasing order of stability

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  3. Range the following free radicals in increasing order of their stabili...

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  4. Arrange the following free radicals in decreasing order of stability:

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  5. Arrange the following carbocations in decreasing order of their stabil...

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  6. Which of the following carbocation is more stable and why?

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  7. Draw the structure of P and Q.

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  8. Compare the basic strength of the following compounds: underset((I))...

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  9. Compare the basic strength of the following compound:

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  10. Which of the following group is most basic in the given compounds"

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  11. Which of the following is a stronger base? Give reason to justify your...

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  12. Which 'H' atom is most acidic in the following compounds.

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  13. Arrange the following in decreasing order of acidity

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  14. The given compound is a strong acid. Justify this statement. X=

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  15. Which of the following reactions is/are feasible?

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  16. Which of the following reaction is feasible?

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  17. Which of the following acids (given below) react with NaHCO(3) and lib...

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  18. Which of the following compounds will exhibit tautomerism?

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  19. Write the tautomers of the following compounds.

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  20. Monocarbonyl compounds have very small percentage enol form at equilib...

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