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What happens when ethanal is treated wit...

What happens when ethanal is treated with methyl magnesium iodide followed by hydrolysis?

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To solve the question of what happens when ethanal (acetaldehyde) is treated with methyl magnesium iodide (a Grignard reagent) followed by hydrolysis, we can follow these steps: ### Step-by-Step Solution: 1. **Identify the Reactants:** - The first reactant is ethanal, which has the chemical formula CH₃CHO. - The second reactant is methyl magnesium iodide, which can be represented as CH₃MgI. ...
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DINESH PUBLICATION-ALDEHYDES AND KETONES -Additional Important Question
  1. Benzophenone does not react with NaHSO(3). Explain.

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  2. Why does formaldehyde undergo Cannizzaro's reaction while acetaldehyde...

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  3. How wil you convert an alkene into an aldehyde containing one carboon ...

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  4. Outline the synthesis of PhCH(2)CH(2)CHO from benzene, ethylene oxide ...

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  5. How will you bring about the following changes :

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  6. Arrange the following in the order of their incresing reactivity towar...

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  7. Arrange the following compounds in order of increasing reactivity towa...

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  8. Name two reagents which can be used to convert gtC = O to gt CH(2) gro...

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  9. Which alkene upon reductive ozonolysis will give acetone as the produc...

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  10. Upon ozonolysis, molecule of a hydrcarbon produces of ethanal and one ...

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  11. Why a benzaldehyde less reactive than acetaldehyde towards nucleophili...

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  12. Formaldehyde gives Cannizzaro's reaction while acetaldehyde does not....

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  13. What happens when ethanal is treated with methyl magnesium iodide foll...

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  14. Identify the compounds [E] to [J] in the following reactions. {:([E]...

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  15. Name the reagent by which most aldehydes can be made to undergo Canniz...

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  16. Which of the following will not give the iodoform test?

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  17. Acetone forms bisulphite compound when heated with sodium bisulphate w...

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  18. The reactions of hydroxylamine with a symmetrical ketone (R(2)C = O) f...

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  19. Compare th relative acidic strengths of hydroxyl amine and am oxime.

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  20. Suggest the suitable reagens for the following conversions:

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