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Explain why is bimolecular dehydration n...

Explain why is bimolecular dehydration not appropriate for the preparation of ethyl methyl ether?

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R G PUBLICATION-ALCOHOLS, PHENOLS AND ETHERS -EXERCISE
  1. Ortho and para nitrophenols are more acidic than phenol. Draw the reso...

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  2. How ethanol is prepared from molasses? Write the various reactions inv...

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  3. Explain why is bimolecular dehydration not appropriate for the prepara...

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  4. 2-methyl, 2-methoxy propane gives 2-iodo 2-methyl propane when treated...

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

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  6. Write the IUPAC name of the following compounds:

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  7. Write the IUPAC name of the following compounds:

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  8. Write the IUPAC name of the following compounds:

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  9. Write the IUPAC name of the following compounds:

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  10. What happens when: Propene reacts with diborane

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  11. What happens when: Prop-2-one reacts with ethyl magnesium bromide

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  12. What happens when: Benzene reacts with oleum in presence of NaOH//H^+.

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  13. What happens when: Salicylic acid reacts with acetic anhydride

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  14. What happens when: Tertiary butanol heated with red hot copper at 573K

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  15. What happens when: Phenol reacts with bromine water

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  16. What happens when: Phenol is oxidised with chromic acid

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  17. What happens when: Ethyl iodide reacts with Sodium ethoxide

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  18. What happens when: Ethoxy benzene is treated with HBr.

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  19. How will you Convert: Ethanol to methanol.

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  20. How will you Convert: Methyl magnesium bromide to 2-methyl propan-2-ol

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