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Which of the following reaction is expec...

Which of the following reaction is expected to readily give a hydrocarbon product in good yield ?

A

`RCOOKunderset("Oxidation")overset("Electrolytic")to`

B

`RCOOAg overset(I_(2))to`

C

`CH_(3)CH_(3)overset(Cl_(2)//hv)to`

D

`(CH_(3))_(3)"CC"loverset(C_(2)H_(5)OH)to`

Text Solution

AI Generated Solution

The correct Answer is:
To determine which reaction is expected to readily give a hydrocarbon product in good yield, we will analyze each of the provided options step by step. ### Step 1: Analyze Option A **Reaction:** Sodium carbonate reacting with electrolytic oxidation. - In this reaction, we focus on the anode where oxidation occurs. - The anion (R-C(=O)O⁻) will undergo oxidation, leading to the formation of R radicals and CO₂. - The R radicals can combine to form a hydrocarbon (R-R), resulting in a hydrocarbon product. **Conclusion for Option A:** This reaction can produce a hydrocarbon in good yield. ### Step 2: Analyze Option B **Reaction:** An ester formation involving R-C(=O)O-Az reacting with I₂. - The reaction with I₂ leads to the formation of R-C(=O)O radical and AzI. - The subsequent steps involve the formation of radicals but ultimately lead to the formation of an ester, not a hydrocarbon. **Conclusion for Option B:** This reaction produces an ester, not a hydrocarbon. ### Step 3: Analyze Option C **Reaction:** Chlorination in the presence of light. - In this reaction, chlorine replaces hydrogen atoms in the hydrocarbon chain through a free radical mechanism. - The product will still contain chlorine and will not be a pure hydrocarbon. **Conclusion for Option C:** This reaction does not produce a hydrocarbon. ### Step 4: Analyze Option D **Reaction:** Reaction of CH₃CH₂Cl with ethanol (C₂H₅OH). - In this reaction, the chlorine leaves to form a carbocation, which is then attacked by the ethanol. - This leads to the formation of an ether, not a hydrocarbon. **Conclusion for Option D:** This reaction produces an ether, not a hydrocarbon. ### Final Conclusion After analyzing all the options, it is clear that **Option A** is the only reaction that readily gives a hydrocarbon product in good yield.
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ICSE-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS-EXERCISE (PART-I OBJECTIVE QUESTIONS)
  1. Weakest acid among the following is

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  2. Ester formation involves the reaction of

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  3. Which of the following reaction is expected to readily give a hydrocar...

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  4. Heating a mixture of sodium benzoate and soda-lime gives

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  5. Which of the following compounds will react with NaHCO(3) solution to ...

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  6. Chlorination of toluene in presence of light and heat followed by trea...

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  7. Which of the following carboxylic acid undergoes decarboxylation easil...

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  8. CH(3)CH(2)COOHunderset("Red P")overset(Br(2))tooverset(NH(3))toY Y i...

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  9. When propionic acid is treated with aqueous sodium bicarbonate, CO(2) ...

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  10. Addition of water to alkynes occurs in acidic medium and in the presen...

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  11. Which of the following compounds is most reactive towards nucleophilic...

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  12. The reagent which does not react with both, acetophenone and benzaldeh...

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  13. Cannizaro's reaction is not given by

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  14. Which product is formed when tht, compound is treated with concen...

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  15. CH(3)-CequivCHunderset(1%HgSO(4))overset(40%H(2)SO(4))toAoverset("isom...

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  16. Compounds A and C in the following reaction are CH(3)CHOunderset((ii...

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  17. Which is the most suitable reagent for the following conversion ? CH...

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  18. Which of the following compounds will give butanone on oxidation with ...

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  19. In clemmensen Reduction, carbonyl compound is treated with

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  20. Correct statement by changing underline part of sentence Aldehydes a...

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