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 Multiple Choice QuestionsShort Answer Type

281. Start from chlorobenzene how will you obtain Aniline.

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282. Start from chlorobenzene how will you obtain Benzene.

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283. What happens when Benzene is heated with iodine in the presence of iodic acid?
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284. What happens when Chlorobenzene is heated with ethanoyl chloride in the presence of AlCl3?
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285. What happens when Iodobenzene is treated with copper powder?
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286. What happens when CCl4 is treated with SbF3?
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287. How the following conversion is carried out?
Chlorobenzene to p-nitrophenol.
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288. How the following conversion is carried out?

Benzene to deuterobenzene
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289. Arrange the following in order of increasing boiling points:

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290.

Secondary alkyl halides are more reactive than primary alkyl halides and tertiary alkyl halides are more reactive than the secondary ones. Explain.


Alkyl groups are electron-repelling (or electron releasing), so larger the number of alkyl groups attached to the carbon atom of the C—X bond, the greater is the electron density on this carbon atom and consequently there is a greater repulsion of the shared electrons towards the X-atom of the C—X bond.




From the above, it is clear that X atom is released as X
 most readily in tertiary halides and least readily in primary halides. Hence, tertiary halides are most reactive, while primary halides are least reactive.

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