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Haloalkanes can easily be prepared from ...

Haloalkanes can easily be prepared from alcohols while aryl halides cannot be prepared from phenol. Explain.

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To understand why haloalkanes can easily be prepared from alcohols while aryl halides cannot be prepared from phenol, we need to analyze the structure and reactivity of both alcohols and phenols. ### Step-by-Step Solution: 1. **Identify the Functional Groups**: - Alcohols have the functional group -OH (hydroxyl group). - Phenols also have the -OH group, but it is attached to an aromatic ring. ...
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PRADEEP-ALCOHOLS, PHENOLS AND ETHERS-CONCEPTUAL QUESTIONS
  1. An organic (A) reacts with PCl(5) to produce another compound (B). (B...

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  2. Arrange the following compounds in the increasing order of the propert...

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  3. Arrange the following in order of their Increasing basicity: H(2)O, ...

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  4. Why (CH(3))(3)COH is less acidic than (CH(3))(3)SiOH although carbon i...

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  5. Draw the structrue and name the product formed if the following alcoho...

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  6. Dehydration of alcohol to form an alkene is always carried out with co...

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  7. Acid catalysed dehydration of t-butanol is faster than that of n-butan...

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  8. Give the structure of the compound, C(C(4)H(8)) which when treated wit...

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  9. 3,3-dimethylbutan-2-ol losses a molecule of water in the presence of c...

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  10. Predict the major product of the following reaction: C(6)H(6)+(CH(3))(...

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  11. Which is a stronger acid, phenol or cresol? Explain.

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  12. How do you account for the fact that unlike phenol, 2,4-dinitrophenol ...

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  13. Unlike phenols, alcohols are easily protonated. Or Alcohols are easily...

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  14. Haloalkanes can easily be prepared from alcohols while aryl halides ca...

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  15. Which of the following is the correct method for synthesising methyl-t...

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  16. Identify the product of the following reaction: CH(3)-underset(CH(3)...

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  17. Ethers are cleaved by acids and not by bases. Explain.

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  18. Anisole is less reactive than phenol towards electrophilic substitutio...

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