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प्रश्न
How will you convert benzene into m – nitrobromobenzene
उत्तर
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संबंधित प्रश्न
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 \[\ce{CH3 - CH^{⊕}2}\]
How will you convert benzene into p – nitrobromobenzene
Arrange the following set of compounds in the order of their decreasing relative reactivity with an electrophile. Give reason.
The relative reactivity of 1°, 2°, 3° hydrogen’s towards chlorination is 1 : 3.8 : 5. Calculate the percentages of all monochlorinated products obtained from 2-methylbutane.
The number ratio of σ and π bonds in benzene is ______.
Mark the incorrect statement from the following:
