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ICSE-HYDROCARBONS -NCERT TEXT-BOOK EXERCISES
- Why is benzene extra ordinarily stable though it contains three double...
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- What are the necessary conditions for any system to be aromatic?
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- Explain why the following systems are not aromatic?
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- Explain why the following systems are not aromatic?
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- Explain why the following systems are not aromatic?
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- How will you convert benzene into (i) p-nitrobromobenzene (ii) m-...
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- How will you convert benzene into (a) p-nitrobromobenzene (b) m-nitrob...
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- How will you convert benzene into (i) p-nitrobromobenzene (ii) m-...
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- How will you convert benzene into (i) p-nitrobromobenzene (ii) m-...
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- In the alkane H3C-CH(2)-C(CH(3))2-CH(2)-CH(CH(3))2, identify 1^(@),2^(...
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- What effect does branching of an alkane chain has on its boiling point...
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- Addition of HBr to propene yields 2-bromopropane, while in the presenc...
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- Write down the products of ozonolysis of 1, 2-dimethylbenzene (o-xylen...
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- Arrange benzene, n-hexane and ethyne in decreasing order of acidic beh...
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- Why does benzene undergo electrophilic substitution reactions easily a...
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- How would you convert the Ethyne compounds into benzene?
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- How would you convert the following compounds into benzene? (i) Ethy...
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- How would you convert the following compounds into benzene? (i) Ethy...
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- Write structures of all the alkenes which on hydrogenation give 2-meth...
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- Arrange the following set of compounds in order of their decreasing re...
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the carbon atom marked by * is `sp^3` hybridised. Therefore, the system is not planar. Although it contains `6-pi` electrons, but they are not delocalised in the ring system. Therefore, it lacks aromatic character.