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The structure of spiropentadiene
The structure of spiropentadiene is shown below; it undergoes a Diels-Alder reaction with two molar equivalents of 1,3-cyclopentadiene. Spiropentadiene is unstable because of its great ring strain. Although cyclopropane rings are retained in the product, they have less ring strain than cyclopropene rings.
What is the chemistry of nitration of naphthalene?
Free radical aromatic substitution - Hydrocarbon The aromatic substitution reactions that follow free radical mechanisms are extremely few and have limited synthetic value. Alt
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Maximum electrons in a d -orbital are: (1) 2 (2) 10 (3) 6 (4) 14 Ans: 10
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