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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.
physical properties
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An isostere is: (1) NO -2 and O 3 (2) No -2 and PO 3- 4 (3) CO 2, N 2 O, NO - 3 (4)Clo - 4 and OCN - Ans: NO -2
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