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Given are cyclohexanol (I), acetic acid ...

Given are cyclohexanol `(I)`, acetic acid `(II),2,4,6-`trinitrophenol `(III)` and phenol `(IV)`. In these the order of decreasing acidic character will be:

A

`III gt IV gt II gt I`

B

`III gt II gt IV gt I`

C

`II gt III gt I gt IV`

D

`II gt III gt IV gt I`

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The correct Answer is:
To determine the order of decreasing acidic character among cyclohexanol (I), acetic acid (II), 2,4,6-trinitrophenol (III), and phenol (IV), we need to analyze the structures and acidity of each compound. ### Step-by-Step Solution: 1. **Identify the Compounds**: - Cyclohexanol (I): An aliphatic alcohol with the structure C6H11OH. - Acetic Acid (II): A carboxylic acid with the structure CH3COOH. - 2,4,6-Trinitrophenol (III): A phenolic compound with three nitro groups attached to the benzene ring, which significantly increases its acidity. - Phenol (IV): A simple aromatic compound with the structure C6H5OH. 2. **Understand Acidity**: - Acidity is determined by the ability of a compound to donate a proton (H+). - Carboxylic acids are generally more acidic than alcohols and phenols due to the stability of their conjugate bases after deprotonation. 3. **Compare Acidity**: - **Cyclohexanol (I)**: As an aliphatic alcohol, it has low acidity. Its conjugate base is not stabilized significantly. - **Acetic Acid (II)**: It is a carboxylic acid and is more acidic than alcohols and phenols. Its conjugate base (acetate ion) is stabilized by resonance. - **Phenol (IV)**: More acidic than cyclohexanol due to resonance stabilization of its conjugate base (phenoxide ion). - **2,4,6-Trinitrophenol (III)**: The presence of three nitro groups (strong electron-withdrawing groups) increases the acidity significantly by stabilizing the conjugate base through resonance and inductive effects. 4. **Order of Acidity**: - **Most Acidic**: 2,4,6-Trinitrophenol (III) - due to strong electron-withdrawing effects from nitro groups. - **Next**: Acetic Acid (II) - as a carboxylic acid, it is more acidic than phenol and cyclohexanol. - **Next**: Phenol (IV) - more acidic than cyclohexanol but less than acetic acid. - **Least Acidic**: Cyclohexanol (I) - the least acidic among the four. 5. **Final Order**: - The order of decreasing acidic character is: - 2,4,6-Trinitrophenol (III) > Acetic Acid (II) > Phenol (IV) > Cyclohexanol (I). ### Conclusion: The correct order of decreasing acidic character is: **2,4,6-Trinitrophenol (III) > Acetic Acid (II) > Phenol (IV) > Cyclohexanol (I)**.

To determine the order of decreasing acidic character among cyclohexanol (I), acetic acid (II), 2,4,6-trinitrophenol (III), and phenol (IV), we need to analyze the structures and acidity of each compound. ### Step-by-Step Solution: 1. **Identify the Compounds**: - Cyclohexanol (I): An aliphatic alcohol with the structure C6H11OH. - Acetic Acid (II): A carboxylic acid with the structure CH3COOH. - 2,4,6-Trinitrophenol (III): A phenolic compound with three nitro groups attached to the benzene ring, which significantly increases its acidity. ...
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