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CH3-overset(O)overset(||)C-CH3+NaOHunder...

`CH_3-overset(O)overset(||)C-CH_3+NaOHunderset(Delta)overset(I_2)rarr(A)`. A will be

A

`CH_3OH`

B

`CHI_3`

C

`CH_3CI_3`

D

`CH_3CH_2CI_3`

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The correct Answer is:
To solve the given reaction, we need to analyze the reaction of acetone with sodium hydroxide (NaOH) in the presence of iodine (I2) under heat. The process involves the formation of an intermediate and subsequent substitution reactions. Here’s a step-by-step breakdown: ### Step 1: Identify the Reactants The reactant given is acetone, which has the structure CH3COCH3. We are reacting it with NaOH and I2. ### Step 2: Deprotonation When acetone reacts with NaOH, the hydroxide ion (OH-) abstracts a proton (H+) from one of the methyl groups adjacent to the carbonyl group. This results in the formation of an enolate ion: \[ \text{CH}_3\text{COCH}_3 + \text{NaOH} \rightarrow \text{CH}_3\text{COCH}_2^{-} + \text{Na}^+ + \text{H}_2\text{O} \] ### Step 3: Resonance Stabilization The enolate ion (CH3COCH2-) is resonance stabilized. The negative charge can be delocalized between the carbonyl oxygen and the carbon atom adjacent to it, which enhances the stability of the enolate. ### Step 4: Iodination The enolate ion (CH3COCH2-) can now attack iodine (I2). The nucleophilic carbon (with the negative charge) attacks one of the iodine atoms, leading to the formation of an iodo compound: \[ \text{CH}_3\text{COCH}_2^{-} + \text{I}_2 \rightarrow \text{CH}_3\text{COCH}_2\text{I} + \text{I}^- \] ### Step 5: Further Iodination If there is excess iodine and NaOH, the process can repeat. The remaining hydrogen on the carbon adjacent to the carbonyl can be abstracted again, leading to another enolate formation, which can then react with another iodine molecule: \[ \text{CH}_3\text{COCH}_2\text{I} + \text{NaOH} + \text{I}_2 \rightarrow \text{CH}_3\text{COCH}\text{I}_2 + \text{Na}^+ + \text{H}_2\text{O} \] ### Final Product The final product (A) of the reaction is: \[ \text{CH}_3\text{COCH}\text{I}_2 \] ### Summary of the Reaction The overall reaction can be summarized as: \[ \text{CH}_3\text{COCH}_3 + \text{NaOH} + \text{I}_2 \xrightarrow{\Delta} \text{CH}_3\text{COCH}\text{I}_2 \]

To solve the given reaction, we need to analyze the reaction of acetone with sodium hydroxide (NaOH) in the presence of iodine (I2) under heat. The process involves the formation of an intermediate and subsequent substitution reactions. Here’s a step-by-step breakdown: ### Step 1: Identify the Reactants The reactant given is acetone, which has the structure CH3COCH3. We are reacting it with NaOH and I2. ### Step 2: Deprotonation When acetone reacts with NaOH, the hydroxide ion (OH-) abstracts a proton (H+) from one of the methyl groups adjacent to the carbonyl group. This results in the formation of an enolate ion: \[ \text{CH}_3\text{COCH}_3 + \text{NaOH} \rightarrow \text{CH}_3\text{COCH}_2^{-} + \text{Na}^+ + \text{H}_2\text{O} \] ...
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NARAYNA-HALOALKANE AND HALOARENES-EXERCISE - 4
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  2. Alkyl halide reacts with an alcoholic solution of ammonia to give a mi...

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  3. Product – I overset("aq KOH")larrC2H5Br overset("alc. KOH")rarr Pro...

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  4. Y is :

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  5. (CH3)2CHCloverset(NaF)underset(H2O)rarr(Y) X+Yoverset(H^+)rarr(Z) ...

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  6. Chlorobenzene towards hydrolysis is ,

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  7. Following equation illustrates C(6)H(5)CI+2NaOHunderset(200atm)overs...

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  8. Alkyl halide on heating with alc. NH3 in a sealed tube results

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  9. Carbylamine is liberated when …….is heated with chloroform and alcohol...

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  10. End product of following sequence of reaction is

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  11. X, Y and Z, respectively are :

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  12. CH2=CHCH2=CH2overset(NBS)rarrA A is

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  13. underset("major")Bunderset(CH3CH2OH)overset(CH3CH2ONa)larrCH3-overset(...

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  15. When an alkylhalide is dissolved in ethanol the following reaction bei...

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  16. Major product of the following SN1 reaction is : H3C-underset(Br)un...

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  17. Ethylene reacts with bromine to from

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  19. An alkyl halide of formula C6H (13)CI on treatment with potassium t-b...

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  20. . A and B

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  21. on treatment with aqueous KOH

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