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underset((ii) H(2)O)overset((i) CO(2))(r...

`underset((ii) H_(2)O)overset((i) CO_(2))(rarr)` In the reaction, product P is

A

B

C

D

`C_(6)H_(5) - overset(O)overset(||)(C ) - C_(6) H_(5)`

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The correct Answer is:
To solve the problem, we need to analyze the reaction of phenylmagnesium bromide (a Grignard reagent) with carbon dioxide (CO2) and water (H2O). Let's break it down step by step: ### Step 1: Identify the Grignard Reagent The given Grignard reagent is phenylmagnesium bromide, which can be represented as C6H5MgBr. Here, C6H5 (the phenyl group) is the organic part, and MgBr is the metal part. **Hint:** Remember that Grignard reagents are highly reactive and can act as nucleophiles due to the presence of a carbon atom with a partial negative charge. ### Step 2: Reaction with Carbon Dioxide When phenylmagnesium bromide reacts with carbon dioxide (CO2), the nucleophilic carbon (C6H5-) attacks the electrophilic carbon of CO2. The structure of CO2 is O=C=O, where the central carbon is electrophilic. **Hint:** Look for the electrophilic center in CO2 that can be attacked by the nucleophile. ### Step 3: Formation of the Intermediate The attack of the phenyl group on CO2 leads to the formation of a carboxylate intermediate. The reaction can be visualized as follows: 1. The phenyl group (C6H5-) attacks the carbon of CO2. 2. This results in the formation of a compound with a carboxylate group (-COO-) and the magnesium bromide complex. The structure can be represented as: \[ C6H5-C(=O)O^{-}MgBr^{+} \] **Hint:** The product formed after the nucleophilic attack will contain a carboxylate group. ### Step 4: Hydrolysis with Water In the next step, the carboxylate intermediate reacts with water (H2O). The water molecule donates a proton (H+) to the carboxylate oxygen, leading to the formation of a carboxylic acid. The reaction can be summarized as: \[ C6H5-C(=O)O^{-} + H2O \rightarrow C6H5-C(=O)OH + MgBrOH \] The final product is benzoic acid (C6H5COOH). **Hint:** Remember that hydrolysis of the carboxylate ion will yield the corresponding carboxylic acid. ### Step 5: Conclusion The product P formed from the reaction of phenylmagnesium bromide with CO2 and water is benzoic acid (C6H5COOH). **Final Answer:** The product P is benzoic acid (C6H5COOH).

To solve the problem, we need to analyze the reaction of phenylmagnesium bromide (a Grignard reagent) with carbon dioxide (CO2) and water (H2O). Let's break it down step by step: ### Step 1: Identify the Grignard Reagent The given Grignard reagent is phenylmagnesium bromide, which can be represented as C6H5MgBr. Here, C6H5 (the phenyl group) is the organic part, and MgBr is the metal part. **Hint:** Remember that Grignard reagents are highly reactive and can act as nucleophiles due to the presence of a carbon atom with a partial negative charge. ### Step 2: Reaction with Carbon Dioxide ...
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NARAYNA-ALDEHYDES, KETONES & CARBOXYLIC ACIDS-EXERCISE -III
  1. The reaction CH(3) CH = CH(2) underset(H^(+))overset(CO + H(2)O)(rar...

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  2. By oxidation with V(2) O(5), which one of the following gives phthalic...

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  3. underset((ii) H(2)O)overset((i) CO(2))(rarr) In the reaction, product...

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  4. Which of the following acids has the smallest dissociation constant

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  5. CH(3)CH(2)COOH overset("Red P/HI")rarr is overset("alc. KOH")rarr "Pro...

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  6. Acetophenone is prepared from :

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  7. Glycerol reacts with potassium bisulphate to produce

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  8. Identify the reactant X and the product Y CH(3) - CO - CH(3) + X rar...

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  9. When m-chlorobenzaldehyde is treated with 50% KOH solution, the produc...

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  10. A and B in the following reaction are R - C - R' overset("HCN/KCN"...

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  11. Which gives lactic acid on hydrolysis after reacting with HCN in KCN ...

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  12. A underset(800^(@)C )overset(Delta)(rarr) CH(2) = C = O , Reactant ' A...

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  13. Laboratory method for the preparation of acetyl chloride is :

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  14. 2CH(3) "COOH" underset(300^(@) C )overset(MnO)(rarr) A, product 'A ' i...

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  15. Which of the aldehyde is most reactive ?

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  16. CH(3) - CH(2) - C equiv CH underset(H(2)SO(4))overset("HgSO"(4))(rarr)...

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  17. R - CH = CH(2) + CO + H(2) underset("High pressure" ) overset("High te...

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  18. The regent used in Gattermann -Koch aldehyde synthesis is

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  19. What is the main reason for the fact that carboxylic acids can undergo...

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  20. On reductive ozonolysis yields

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