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Why alkyl halides are not generally prep...

Why alkyl halides are not generally prepared in laboratory by free radical halogenation of alkanes?

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For the preparation of alkyl halides in the laboratory, free radical halogenation of alkanes is not a suitable method since it results in the formation of many isomeric monosubstituted products through substitution of different kinds of hydrogen atoms. Moreover, poly halogenation may also take place.
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AAKASH SERIES-ALKYL AND ARYL HALIDES-EXAMPLES
  1. How many stereo isomers are possible for CH3 CH = CH - underset...

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  2. Haloakanes react with KCN to form alkyl cyanides as main product while...

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  3. Why alkyl halides are not generally prepared in laboratory by free rad...

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  4. R-Cl is hydrolysed to R-OH slowly but the reaction is rapid in presenc...

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  5. Optically active 2-iodobutane on treatment with sodium iodide in aceto...

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  6. Expain the formation of the two products in the following reaction : ...

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  7. Why the chlorine atom in vinyl chloride is nonreactive?

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  8. Allyl iodide can be obtained from allyl chloride. Explain.

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  9. Predict the order of reactivity of the following compounds in SN1 and ...

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  10. Write the structures of major and minor products formed when 3-chloro-...

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  11. How do you distinguish between CH3CH = CHCl , CH3CH2Cl and CH2=CH-CH2C...

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  12. In the following pairs of halogen compounds, which would undergo SN2 r...

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  13. Predict the order of reactivity of the following compounds in SN1 and ...

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  14. Which alkyl halide from the following pairs would you expect to react ...

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  15. In the following pairs of halogen compounds, which compound undergoes ...

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  16. Identify A, B, C, D, E, R and R' in the following:

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  17. What is teflon ? How is it prepared ?

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  18. How will you distinguish between chloroform and carbon tetrachloride ?

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  19. How iodoform is distinguished from chloroform?

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  20. Among the three isomeric dichlorobenzenes , which has the highest...

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