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Question
How will you convert benzene into m – nitrobromobenzene
Solution
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RELATED QUESTIONS
Why is benzene extra ordinarily stable though it contains three double bonds?
Write down the products of ozonolysis of 1, 2-dimethylbenzene (o-xylene). How does the result support Kekulé structure for benzene?
Arrange the following carbanions in order of their decreasing stability.
(A) H3C – C ≡ C–
(B) H – C ≡ C–
(C) \[\ce{H3C - C\overset{-}{H2}}\]
Which of the following are correct?
(i) \[\ce{CH3 - O - CH^{⊕}2}\] is more stable than \[\ce{CH3 - CH^{⊕}2}\]
(ii) (CH3)2CH⊕ is less stable than \[\ce{CH3 - CH2 - CH^{⊕}2}\]
(iii) \[\ce{CH3 = CH2 - CH^{⊕}2}\] is more stable than \[\ce{CH3 - CH2 - CH^{⊕}2}\]
(iv) \[\ce{CH2 - CH^{⊕}}\] is more stable than \[\ce{CH3 - CH^{⊕}2}\]
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