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The p-isomer of dichlorobenzene has high...

The p-isomer of dichlorobenzene has higher melting point than O-and M-isomer. Why ?

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The structures of three isomeric dichlorobenzenes are as follows:

The p-isomer being more symmetrical fits closely in the crystal lattice and thus has stronger intra-molecular forces of attraction than o and n-isomers. Since during melting or dissolution, the crystal lattice breaks, therefore, a larger amount of energy is needed to melt or dissolve the p-isomer than the corresponding o-and m-isomers. In other words, the melting point of the p-isomer is higher and its solubility lower than the corresponding o and m-isomers.
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BETTER CHOICE PUBLICATION-HALOALKANES AND HALOARENES-QUESTIONS
  1. Define retention.

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  2. The p-isomer of dichlorobenzene has higher melting point than O-and M-...

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  3. The p-isomer of dichlorobenzene has higher melting point than O-and M-...

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  4. Give reasons : Boiling point of alkyl bromide is higher than alkyl c...

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  5. Give reasons : Alkyl halides are better solvents than aryl halides.

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  6. Give reasons : Haloalkanes used as solvents in industry are chloro ...

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  7. What are ambident uncleophiles ? Explain with an example.

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  8. Alkyl Chloride is more reactive than chlorobenzene towards nucleophili...

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  9. With the help of polarity of the carbon halogen bond show that aryl ha...

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  10. Why are haloarenes more stable than haloalkanes ?

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  11. Why do alkyi haldies undergo hydrolysis more readily than aryl halides...

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  12. With the help of resonance show that aryl halides are lesser reactive ...

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  13. With the help of hybridisation show that aryl halides are lesser react...

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  14. With the help of polarity of the carbon halogen bond show that aryl ha...

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  15. Why does electrophilic substitution take place at ortho and para posit...

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  16. Why does electrophilic substitution take place at ortho and para posit...

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  17. Haloarene is ortho and para directing Explain.

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  18. Write short notes on : Wurtz reaction

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  19. Write Fittig reaction.

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  20. Write short notes on : Friedel Craft's reaction

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