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How would you convert the following comp...

How would you convert the following compounds into benzene?
(i) Ethyne
(ii) Ethene
(iii) Hexane

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To convert the given compounds into benzene, we can follow these steps: ### (i) Conversion of Ethyne to Benzene 1. **Starting Material**: Take 3 moles of ethyne (C₂H₂). 2. **Reaction Conditions**: Pass the ethyne through a red-hot iron tube. 3. **Reaction Type**: A polymerization reaction occurs where the ethyne molecules combine to form benzene (C₆H₆). 4. **Final Product**: The result is benzene. ### (ii) Conversion of Ethene to Benzene 1. **Starting Material**: Begin with ethene (C₂H₄). 2. **First Step**: Convert ethene to ethyne. - **Reagents**: Add bromine (Br₂) in the presence of carbon tetrachloride (CCl₄) to the ethene. This adds bromine across the double bond. - **Second Step**: Remove the bromine using alcoholic KOH, which acts as a dehydrohalogenating agent, resulting in the formation of ethyne. 3. **Next Step**: Use the ethyne obtained from the previous step. 4. **Final Step**: Pass the ethyne through a red-hot iron tube to convert it into benzene. ### (iii) Conversion of Hexane to Benzene 1. **Starting Material**: Take hexane (C₆H₁₄). 2. **First Step**: Cyclization of hexane. - **Reagents**: Pass hexane over chromium oxide (CrO₃) or aluminum oxide (Al₂O₃) in the presence of molybdenum oxide (MoO₃). - **Result**: This process leads to the formation of cyclohexane (C₆H₁₂). 3. **Next Step**: Convert cyclohexane to benzene. - **Process**: Remove three hydrogen atoms from cyclohexane. 4. **Final Product**: The result is benzene. ### Summary of Conversions - Ethyne → Benzene: 3 moles of ethyne → red-hot iron tube → Benzene. - Ethene → Ethyne → Benzene: Ethene + Br₂ → Ethyne → red-hot iron tube → Benzene. - Hexane → Cyclohexane → Benzene: Hexane → CrO₃/Al₂O₃/MoO₃ → Cyclohexane → remove H → Benzene. ---

To convert the given compounds into benzene, we can follow these steps: ### (i) Conversion of Ethyne to Benzene 1. **Starting Material**: Take 3 moles of ethyne (C₂H₂). 2. **Reaction Conditions**: Pass the ethyne through a red-hot iron tube. 3. **Reaction Type**: A polymerization reaction occurs where the ethyne molecules combine to form benzene (C₆H₆). 4. **Final Product**: The result is benzene. ...
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NCERT ENGLISH-HYDROCARBONS-EXERCISE
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  2. Propanal and pentan-3-one are the ozonolysis products of an alkene? Wh...

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  3. Write chemical equations for combustion reaction of the following hydr...

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  4. Draw the cis and trans structures of hex-2-ene. Which isomer will have...

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  5. Why is benzene extra ordinarily stable though it contains three double...

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  6. What are the necessary conditions for any system to be aromatic?

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  7. Explain why the following systems are not aromatic?

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  8. How will you convert benzene into (i) p-nitrobromobenzene (ii) m-...

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  9. In the alkane H3C-CH(2)-C(CH(3))2-CH(2)-CH(CH(3))2, identify 1^(@),2^(...

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  10. What effect does branching of an alkane chain has on its boiling point...

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  11. Addition of HBr to propene yields 2-bromopropane, while in the presenc...

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  12. Write down the products of ozonolysis of 1, 2-dimethylbenzene (o-xylen...

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  13. Arrange benzene, n-hexane and ethyne in decreasing order of acidic beh...

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  14. Why does benzene undergo electrophilic substitution reactions easily a...

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  15. How would you convert the following compounds into benzene? (i) Ethy...

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  16. Write structures of all the alkenes which on hydrogenation give 2-meth...

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  17. Arrange the following set of compounds in order of their decreasing re...

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  18. Out of benzene, m–dinitrobenzene and toluene which will undergo nitrat...

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  19. Suggest the name of a Lewis acid other than anhydrous aluminium chlori...

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  20. Why is Wurtz reaction not preferred for the preparation of alkanes con...

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