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Which one is the most acidic compound?...

Which one is the most acidic compound?

A

B

C

D

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The correct Answer is:
To determine which compound is the most acidic among the given options, we need to analyze the effects of substituents on the acidity of phenolic compounds. Here’s a step-by-step solution: ### Step 1: Identify the Compounds All the compounds in the question are phenolic compounds, meaning they contain a benzene ring with a hydroxyl (OH) group. The presence of different substituents on the benzene ring will influence their acidity. ### Step 2: Understand Acidity in Phenolic Compounds Acidity in phenolic compounds is influenced by the ability of the compound to donate a proton (H+). The strength of the O-H bond in the hydroxyl group is crucial; if the bond is weak, the compound can easily release H+, making it more acidic. ### Step 3: Analyze the Effect of Substituents - **Electron Donating Groups (EDGs)**: These groups, such as -CH3 (methyl), donate electrons to the benzene ring. This donation stabilizes the ring but makes the O-H bond stronger, making it harder to release H+ and thus decreasing acidity. - **Electron Withdrawing Groups (EWGs)**: Groups like -NO2 (nitro) withdraw electrons from the benzene ring. This withdrawal weakens the O-H bond, making it easier to release H+ and thus increasing acidity. ### Step 4: Compare the Given Options - **Option A**: Contains a methyl group (-CH3), which is an EDG. This makes it less acidic. - **Option B**: Is phenol with no substituents, serving as a baseline for acidity. - **Option C**: Contains one nitro group (-NO2), which is an EWG. This increases acidity compared to phenol. - **Option D**: Contains three nitro groups. The presence of multiple EWGs significantly increases the acidity of this compound. ### Step 5: Determine the Most Acidic Compound Since option D has three nitro groups, which are strong electron withdrawing groups, it will be the most acidic among all the options. The presence of multiple EWGs will greatly enhance the ability of the compound to donate H+. ### Conclusion The most acidic compound among the given options is **Option D** (the compound with three nitro groups). ---
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AAKASH INSTITUTE ENGLISH- ALCOHOLS, PHENOLS AND ETHERS-Assignment Section - C (Previous Years questions)
  1. Which one is the most acidic compound?

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  2. The heating of phenyl-methyl ethers with HI produces

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  3. The reaction can be classified as

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  4. Which of the following reagents would distinguish ciscyclopenta -1,2-d...

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  5. Reaction of phenol with chloroform in presence of dilute sodium hydrox...

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  6. Which of the following is not the product of dehydration of

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  7. Which of the following reaction(s) can be used for the preparation of ...

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  8. The reaction CH(3)-underset(CH(3))underset(|)overset(CH(3))overset(|...

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  9. Among the following sets of reactants which one produces anisole?

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  10. Identify Z in the sequence of reactions : CH(3)CH(2)CH=CH(2)underse...

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  11. Among the following ethers, which one will produce methyl alcohol on t...

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  12. In the following reaction The major product is

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  13. In the following reactions . ltb rgt CH3-overset(CH3)overset(|)CH-unde...

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  14. Which one of the following compounds has the most acidic nature ?

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  15. Which one of the following is most reactive towards electrophillic rea...

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  16. Among the following four compounds (a) Phenol (b) methyl phenol ...

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  17. When glycerol is treated with excess of HI, it produces -

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  18. Which one of the following compounds will be most readily dehydrated?

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  19. Which of the following conformers for ethylene glycol is most stable ?

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  20. Consider the following reaction "Ethanol" overset(PBr(3))to X overset...

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