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Discuss the nature of C-X bond in the ha...

Discuss the nature of C-X bond in the haloarenes.

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To discuss the nature of the C-X bond in haloarenes, we can break down the explanation into several key points: ### Step-by-Step Solution: 1. **Definition of Haloarenes**: - Haloarenes are compounds where a halogen atom (X) is bonded to an aromatic ring, specifically a benzene ring. The carbon atom of the benzene ring is directly bonded to the halogen. 2. **Hybridization of Carbon**: ...
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NCERT EXEMPLAR-HALOALKANES AND HALOARENES-Haloalkanes And Haloarenes
  1. tert-Butylbromide reacts with aq. NaOH by S(N)1 mechanism while n-buty...

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  2. Predict the major product formed when HCl is added to isobutylene, Exp...

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  3. Discuss the nature of C-X bond in the haloarenes.

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  4. How can you obtain iodoethane from ethanol when no other iodine contai...

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  5. Cyanide ion acts as an ambident nucleophille. From which end it acts a...

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  6. Match the compounds given in column I with the effects given in Column...

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  7. Match the items of Column I and Column II

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  8. Match the structures of compounds given in Column I with the classes o...

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  9. Match the reactions given in Column I with the types of reactions give...

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  10. Match the structures given in Column I with the names in Column II

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  11. Match the reactions given in Column I with the names givn in Column II...

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  12. Assertion ( A) Phosphorus chlorides ( tri and penta) are preferred ove...

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  13. Assertion( A) The boiling points of alkyl halides decrease in the orde...

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  14. Assertion( A) KCN reacts with methyl chloride to give methyl isocyanid...

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  15. Assertion (A) tert-butyl bromide undergoes Wurtz reaction to give 2,2,...

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  16. Assertion (A) Presence of a nitro group at ortho or para position incr...

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  17. Assertion: In monohaloarenes, further electrophilic substitution occur...

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  18. Assertion: Aryl iodides can be prepared by reaction of arenes with iod...

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  19. Assertion: It is difficult to replace chlorine by -OH in chlorobenzene...

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  20. Assertion (A) Hydrolysis of (-)-2-bromooctane proceeds with inversion ...

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