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How will you convert benzene into: (i...

How will you convert benzene into:
(i) p-nitrobromobenzene
(ii) m-nitrobromobenzene

Text Solution

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(ii)Here, since the substituents are at m-position w.r.t. to each other , therefore, the first substituent in the benzene ring should be m-directing (i.e., `NO_2`) and then the other group (i.e., Br) should be introduced .Therefore, the sequence of reactions is
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PRADEEP-HYDROCARBONS-NCERT EXEMPLAR PROBLEMS WITH ANSWERS, HINTS AND SOLUTIONS (SHORT ANSWER QUESTIONS)
  1. Why do alkenes prefer to undergo electrophilec addition reaction while...

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  2. Alkynes on reduction with sodium in liquid ammonia form trans alkenes....

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  3. Rotation around carbon-carbon single bond of ethane is not completely ...

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  4. Draw Newman and sawhorse projections for the eclipsed and staggered co...

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  5. The intermediate carbocation formed in the reactions of HI,HBr, and HC...

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  6. What will be the product obtained as a result of the following reactio...

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  7. How will you convert benzene into: (i) p-nitrobromobenzene (ii) ...

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  8. Arrange the following set of compounds in the order of their decreasin...

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  9. Despite their-I effect, halogens are o- and p- directing in haloarenes...

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  10. Why does presence of a nifro group make the benzene ring less reactive...

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  11. Suggest a route for the preparation of nitrobenzene starting from acet...

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  12. Predict the major product(s) of the following reactions and explain th...

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  13. Nucleophiles and electrophiles are reaction intermediates having elect...

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  14. The relative reactivity of 1^(@), 2^(@) and 3^(@) hybrogen's towards c...

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  15. Write the structures and names of products obtained in the reactions o...

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  16. Write hydrocarbon radicals that can be formed as intermediates during ...

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  17. An alkane C(8)H(18) is obtained as the only product on subjecting a pr...

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  18. The ring systems having following characteristics are aromatic. (i) ...

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  19. Which of the following compounds are aromatic according to Huckle's ru...

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  20. Suggest a route to prepare ethyl hydrogensulphate (CH(3)-CH(2)-OSO(2)-...

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