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The groups which when present in para po...

The groups which when present in para position tend to decrease the acidity of phenol are-

A

`-NO_(2)`

B

`-CN`

C

`-OCH_(3)`

D

`-F`

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The correct Answer is:
To determine which groups, when present in the para position of phenol, decrease its acidity, we need to analyze the effects of various substituents on the acidity of phenol. ### Step-by-Step Solution: 1. **Understanding Phenol Structure**: - Phenol has a hydroxyl group (-OH) attached to a benzene ring. The structure can be represented as: \[ \text{C}_6\text{H}_5\text{OH} \] 2. **Acidity of Phenol**: - The acidity of phenol is influenced by the substituents present on the benzene ring. The acidity is determined by the stability of the phenoxide ion (the conjugate base formed when phenol donates a proton). 3. **Electron-Withdrawing vs. Electron-Donating Groups**: - **Electron-Withdrawing Groups (EWGs)**: These groups stabilize the negative charge on the phenoxide ion, increasing acidity. They typically exhibit a -I (inductive) or -R (resonance) effect. - **Electron-Donating Groups (EDGs)**: These groups destabilize the negative charge on the phenoxide ion, decreasing acidity. They typically exhibit a +I (inductive) or +R (resonance) effect. 4. **Analyzing the Given Groups**: - **NO2 (Nitro group)**: This is an electron-withdrawing group (-I and -R effect). It increases acidity. (Not our answer) - **CN (Cyano group)**: This is also an electron-withdrawing group (-I and -R effect). It increases acidity. (Not our answer) - **OCS3 (Methoxy group)**: This group has a lone pair on oxygen, which contributes a +R effect, making it an electron-donating group. It decreases acidity. (This is our answer) - **Fluorine (F)**: Although it is highly electronegative and has a -I effect, it also has a +R effect due to resonance. However, its overall effect is still electron-withdrawing, thus increasing acidity. (Not our answer) 5. **Conclusion**: - The group that decreases the acidity of phenol when present in the para position is **OCS3 (Methoxy group)**. ### Final Answer: The groups which, when present in para position, tend to decrease the acidity of phenol are **OCS3 (Methoxy group)**.
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Which of the following will increase the acidity of phenol ?

Assertion (A) Presence of a nitro group at ortho or para position increases the reactivity of haloarenas towards nucleophilic substitution. Reason (R ) Nitro group, being an electron withdrawing group decreases the electron density over the benzene ring.

Assertion: Presence of a nitro group at ortho or para position increases the reactivity of haloarenes towards nucleophilic substitution. Reason: Nitro group, being an electron withdrawing group decreases the electron density over the benzene ring.

Which of the following substituents will decrease the acidic strength of phenol?

BANSAL-GENERAL ORGANIC CHEMISTRY-Exercise 3
  1. The groups which when present in para position tend to decrease the ac...

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  2. Write stability order of following intermediates:

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  3. Write stability order of following intermediates:

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  4. Write Stability order of following intermediates:

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  5. Rank the following sets of intermediates in increasing order of their ...

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  6. In each of the following pairs of ions which ion is more stable:

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  7. Rank the following sets of intermediates in increasing order of their ...

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  8. Rank the following sets of intermediates in increasing order of their ...

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  9. Compare heat of hydrogenation (Decreasing order)

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  10. Write increasing order of heat of hydrogenation:

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  11. In which of the following pairs, indicated bond is of greater strength...

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  12. Consider the given reaction: In the above reaction which one of t...

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  13. Write correct order of acidic strength of following compounds: (i). ...

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  14. Write increasing order of basic strength of following: (i). (a) F^(ɵ...

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  15. Record the following sets of compounds according to increasing pK(a)(=...

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  16. Explain which is a stronger acid CH(3)CH(3)&BrCH(2)NO(2)

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  17. Which of the following pairs has higher resonance energy: (a). CH(3)...

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  18. Choose the more stable alkene in each of the following pair. Explain y...

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  19. Which of the followig pairs has higher resonance energy: (a). (b)...

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  20. Rank the following sets of intermediates in increasing order of their ...

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