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Acyl halides are prepared by the action ...

Acyl halides are prepared by the action of _____on carboxylic acids.

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To answer the question, "Acyl halides are prepared by the action of _____ on carboxylic acids," we can follow these steps: ### Step 1: Identify the reactants We start with carboxylic acids, which have the general formula RCOOH, where R is an alkyl or aryl group. ### Step 2: Identify the reagents used to convert carboxylic acids to acyl halides Acyl halides can be synthesized from carboxylic acids using different reagents. Common reagents include: - Thionyl chloride (SOCl2) ...
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PRADEEP-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS -TEST YOUR GRIP (II. FILL IN THE BLANKS)
  1. O- Xylene on oxidation with alkaline KMnO(4) followed by acidificati...

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  2. Enthanenitrile on hydrolysis gives.

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  3. Grignard reagents give alkane, on reaction with :

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  4. pK(a) and K(a) of an acid are connected by the relation …….. .

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  5. Higher theor lower the of an acid, stronger is the acid.

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  6. Ethanoic acid is a weaker acid than methanoic acid due toof the methyl...

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  7. Chloroacetic acid si a stronger acid than acetic acid due toof the chl...

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  8. m-Methoxybenzoic acid is aacid than p-methoxybenzoic acid due toof the...

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  9. Acyl halides are prepared by the action of on carboxylic acids.

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  10. Amides are least reactive of the acid derivatives towardsreactions.

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  11. is ivolved when an amide is heated with a dilute solution of sodium hy...

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  12. Esters on treatment with excess of grignard reagents followed by acid ...

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  13. When ammonium acetate is heatedis formed.

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  14. When eithyl acetate is treated withacetoacetic ester is formed.

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  15. Kolbe's electrolysis of potassium succinate gives CO(2) and ……………………

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  16. Hell-Volhard-Zelinsky reaction involves the replacement of an ...........

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  17. Nitration of benzoic acid gives m-nitrobenzoic acid.

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  18. Benzoic acid does not undergo Friedel-Crafts reaction due to......... ...

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  19. Formic acid reducesbut acetic acid does not.

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  20. Vinegar is a dilute solution of.

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