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Why is the ester distilled as fast as it...

Why is the ester distilled as fast as it is formed during the preparation of esters from the reaction between alcohol and carboxylic acid ?

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Because the reaction is reversible and boiling point of ester is less than both the carboxylic acid and alcohol from, which it is formed.
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BETTER CHOICE PUBLICATION-ORGANIC COMPOUND WITH FUNCTIONAL GROUP CONTANING OXYGEN-II-Question Bank (12.8 Chemical Reaction)
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  2. Write short note on Kolbe's electrolysis.

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  3. Write short note on Hunsdicker reaction.

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  4. Write short note on Esterification

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  6. Carboxylic acids do not give the characteristic reactions of carbonyl ...

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  7. Why carboxylic acids do not give characteristic reactions of -OH group...

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  8. Why do carboxylic acids do not form oximes with NH2OH (hydroxyl amine)...

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  9. Give simple chemical tests to distinhuish between the following pairs ...

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  10. Give simple chemical tests to distinhuish between the following pairs ...

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  11. Give simple chemical tests to distinhuish between the following pairs ...

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  12. Give simple chemical tests to distinhuish between the following pairs ...

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  13. Give simple chemical tests to distinhuish between the following pairs ...

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  14. What makes ethanoic acid a stronger acid than ethanol ?

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  15. Complete the following: 2CH3COOH+ Na2CO3 rarr

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  16. Complete the following: 2CH3COOH+2Na rarr

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  17. Complete the following Reactions. CH(3)COOH + NaOH rarr

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  18. Complete the following Reactions. CH(3)COOH + NH(3) rarr

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  19. Complete the following reaction:-

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  20. Complete the following reaction:-

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