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Among the following amines, the stronges...

Among the following amines, the strongest Bronsted base is….

A

B

`NH_(3)`

C

D

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To determine which among the given amines is the strongest Bronsted base, we will analyze each option based on their structure and the presence of electron-donating or electron-withdrawing effects. ### Step 1: Understand Bronsted Bases A Bronsted base is defined as a substance that can accept protons (H⁺ ions). The strength of a Bronsted base is influenced by the availability of lone pairs of electrons on the nitrogen atom, as well as the presence of any electron-withdrawing or electron-donating groups that may stabilize or destabilize the lone pair. ### Step 2: Analyze Aniline - **Structure**: Aniline (C₆H₅NH₂) has an amino group (-NH₂) attached to a benzene ring. - **Effect of the Benzene Ring**: The lone pair of electrons on the nitrogen can be delocalized into the aromatic ring. This delocalization reduces the availability of the lone pair for protonation, making aniline less basic. - **Conclusion**: Aniline is a weak base compared to ammonia. ### Step 3: Analyze Ammonia - **Structure**: Ammonia (NH₃) has a lone pair of electrons on the nitrogen atom. - **No Delocalization**: There are no aromatic rings or other groups that can delocalize the lone pair, making it readily available for protonation. - **Conclusion**: Ammonia is a stronger base than aniline. ### Step 4: Analyze Pyrrole - **Structure**: Pyrrole (C₄H₄NH) contains a nitrogen atom in a five-membered ring with two double bonds. - **Effect of Conjugation**: The lone pair on nitrogen is involved in the aromaticity of the ring, which means it is less available for protonation. - **Conclusion**: Pyrrole is a weak base due to the involvement of the lone pair in maintaining aromatic stability. ### Step 5: Analyze Pyrrolidine - **Structure**: Pyrrolidine (C₄H₉N) is a saturated five-membered ring containing nitrogen. - **No Delocalization**: The nitrogen's lone pair is not involved in any resonance or delocalization, making it highly available for protonation. - **Conclusion**: Pyrrolidine is the strongest base among the options provided. ### Final Conclusion Among the given amines, the strongest Bronsted base is **pyrrolidine**.

To determine which among the given amines is the strongest Bronsted base, we will analyze each option based on their structure and the presence of electron-donating or electron-withdrawing effects. ### Step 1: Understand Bronsted Bases A Bronsted base is defined as a substance that can accept protons (H⁺ ions). The strength of a Bronsted base is influenced by the availability of lone pairs of electrons on the nitrogen atom, as well as the presence of any electron-withdrawing or electron-donating groups that may stabilize or destabilize the lone pair. ### Step 2: Analyze Aniline - **Structure**: Aniline (C₆H₅NH₂) has an amino group (-NH₂) attached to a benzene ring. - **Effect of the Benzene Ring**: The lone pair of electrons on the nitrogen can be delocalized into the aromatic ring. This delocalization reduces the availability of the lone pair for protonation, making aniline less basic. ...
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  • Which of the following is the strongest Bronsted base?

    A
    B
    C
    D
  • Which of the following is the strongest Bronsted base ?

    A
    B
    C
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  • Which one of the following anionc is the strongest Bronsted base ?

    A
    `CIO^(-)`
    B
    `CIO_(2)^(-)`
    C
    `CIO_(3)^(-)`
    D
    `CIO_(4)^(-)`
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