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Why is Wurtz reaction not suitable for t...

Why is Wurtz reaction not suitable for the preparation of odd number alkanes ?

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Wurtz reaction is generally used for making symmetrical alkanes containing even number of carbon atoms. For example,

If we try to make as alkane with odd number of carbon atoms by this method, the yield of desired alkane is very poor as two more alkanes are also obtained as by products. Further separation of desired alkane from byproducts is also difficult. For example if we try to make propare by Wurtz reaction, ethane and butane are formed as by products.
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BETTER CHOICE PUBLICATION-HALOALKANES AND HALOARENES-QUESTIONS
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  2. What do you mean by dehydrohalogenation reaction ?

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  3. Why is Wurtz reaction not suitable for the preparation of odd number a...

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  5. Write the following reactions : Carbylamine reaction.

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  6. Write following name reactions : Riemer Tiemann reactioin.

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  7. Explain the following : Hoffmann amonolysis

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  8. Write the following reactions : Williamson’s synthesis

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  9. Explain the following reactions: Diazotisation reaction.

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  10. Alkyl halides are amongst the most reactive of the organic compounds. ...

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  11. Alkyl halides are regarded as synthetic tools in the hands of a chemis...

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  12. How do the products differ when ethyl bromide reacts separately with a...

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  13. What is the purpose of anhydrous ZnCl2 in the preparation of haloalkan...

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  14. What happens when : Ethyl chloride is treated with (aq) KOH.

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  15. What happens when : Methyl chloride is treated with KCN.

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  16. Methyl bromide is treated with sodium in the presence of dry ether.

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  17. What happens when : n-butyl chloride is treated with alcoholic KOH.

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  18. What happens when an ethyl bromide reacts with : Ag NO2

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  19. What happens when an ethyl bromide reacts with : Ag CN (alc.) ?

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  20. Haloalkanes undergo nucleophilic substitution reactions while haloaren...

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