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Which of the following does not give alk...

Which of the following does not give alkane

A

Reaction of `CH_3` I with Na in sodalime

B

Reaction of sodium acetate with sodalime

C

Electrolysis of concentrated sodium acetate solution

D

Reaction of ethyl chloride with alco. KOH

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The correct Answer is:
To solve the question "Which of the following does not give alkane?", we will analyze each of the given reactions step by step. ### Step 1: Analyze the first reaction (Methyl iodide with sodium in soda lime) - **Reaction**: 2 CH3I + 2 Na → C2H6 (Ethane) + 2 NaI - **Explanation**: Methyl iodide (CH3I) reacts with sodium in the presence of soda lime to produce ethane (C2H6). This is a Wurtz reaction, which typically yields alkanes. ### Step 2: Analyze the second reaction (Sodium acetate with soda lime) - **Reaction**: CH3COONa + NaOH (soda lime) → CH4 (Methane) + Na2CO3 - **Explanation**: Sodium acetate undergoes decarboxylation in the presence of soda lime, resulting in the formation of methane (CH4), which is also an alkane. ### Step 3: Analyze the third reaction (Electrolysis of concentrated sodium ester solution) - **Reaction**: RCOONa (sodium ester) → R-R + CO2 + NaOH - **Explanation**: The electrolysis of sodium esters leads to the formation of alkanes through the Kolbe electrolysis process. For example, the electrolysis of sodium acetate can yield ethane (C2H6). ### Step 4: Analyze the fourth reaction (Ethyl chloride with alcoholic KOH) - **Reaction**: C2H5Cl + KOH (alcoholic) → C2H4 (Ethene) + KCl + H2O - **Explanation**: Ethyl chloride reacts with alcoholic KOH to undergo elimination, producing ethene (C2H4), which is an alkene, not an alkane. ### Conclusion: After analyzing all the reactions, we find that the fourth reaction (ethyl chloride with alcoholic KOH) does not produce an alkane; instead, it produces an alkene (ethene). ### Final Answer: The reaction that does not give an alkane is the fourth one: Ethyl chloride with alcoholic KOH. ---

To solve the question "Which of the following does not give alkane?", we will analyze each of the given reactions step by step. ### Step 1: Analyze the first reaction (Methyl iodide with sodium in soda lime) - **Reaction**: 2 CH3I + 2 Na → C2H6 (Ethane) + 2 NaI - **Explanation**: Methyl iodide (CH3I) reacts with sodium in the presence of soda lime to produce ethane (C2H6). This is a Wurtz reaction, which typically yields alkanes. ### Step 2: Analyze the second reaction (Sodium acetate with soda lime) - **Reaction**: CH3COONa + NaOH (soda lime) → CH4 (Methane) + Na2CO3 ...
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ERRORLESS-HYDROCARBONS-ASSERTION & REASON
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  3. Assertion : Tropylium cation is aromatic in nature Reason : The only...

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  4. Assertion:Cyclobutane is less stable than cyclopentane. Reason : Pre...

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  5. Assertion : Pyrrole is an aromatic heterocyclic compound Reason : ...

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  6. Assertion : CH(4) does not react Cl(2) in dark. Reason: Chlorinat...

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  7. Assertion : Alkyl benzene is not prepared by Friedel- Crafts alkylatio...

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  8. Assertion : 2-Bromobutane on reaction with sodium ethoxide in ethanol ...

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  9. Assertion: Styrence on reaction with HBr gives 1-bromo-1-phenylethane ...

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  10. Assertion :Iodination of alkanes is reversible Reason:Iodination is ...

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  11. Assertion:Freezing point of neopentane is more than n-pentane. Reaso...

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  12. Assertion : The presence of Ag^(+) enhance the solubility of alkenes i...

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  13. Assertion : Propene reacts with HBr in presence of benzoyl peroxide to...

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  14. A) Addition of HBr on 2-butene gives two isomeric products. R) Addit...

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  15. Assertion:Aryl halides are less reactive towards substitution of halog...

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