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Show how will you synthesise: (i) 1-ph...

Show how will you synthesise:
(i) 1-phenylethanol from a suitable alkene.
(ii) cyclohexylmethanol using an alkyl halide by an `S_(N)2` reaction.
(iii) pentan-1-ol using a suitable alkyl halide?

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How will you synthesise 1-Phenylethanol from a suitable alkene.

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The order of reactivities of the following alkyl halides for a S_N2 reaction is

The order of reactivities of the following alkyl halides for a S_N2 reaction is

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NCERT TELUGU-ALCOHOLS , PHENOLS AND ETHERS-EXERCISE
  1. Write the mechanism of hydration of ethane to yield ethanol.

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  2. You are given benzene, conc. H(2)SO(4)and NaOH Write the equations f...

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  3. Show how will you synthesise: (i) 1-phenylethanol from a suitable al...

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  4. Give two reactions that show the acidic nature of phenol. Compare acid...

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  5. Explain Ortho nitrophenol is more acidic than Ortho methoxyphenol.

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  6. Explain OH group attached to benzene ring activates it towards electro...

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  7. 7 Give equations of the following reactions: (i) Oxidation of propan...

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  8. Explain the following with an example. (i) Kolbe’s reaction. (ii) ...

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  9. Write the mechanism of acid dehydration of ethanol to yield ethene

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  10. How are the following conversions carried out? (i) Propene → Propan-...

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  11. 1 Name the reagents used in the following reactions: (i) Oxidation o...

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  12. 2 Give reason for the higher boiling point of ethanol in comparison to...

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  13. Give IUPAC names of the following ethers: (i) C(2)H(5)OCH(2) -under...

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  14. Write the names of reagents and equations for the preparation of the f...

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  15. Illustrate with examples the limitations of Williamson synthesis for t...

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  16. How is 1-propoxypropane synthesised from propan-1-ol? Write mechanism ...

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  17. Preparation of ethers by acid dehydration of secondary or tertiary alc...

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  18. Write the equation of the reaction of hydrogen iodide with: (i) 1-pr...

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  19. Explain the fact that in aryl alkyl ethers (i) the alkoxy group activa...

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  20. Write the mechanism of the reaction of HI with methoxymethane.

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