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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.
In lab, you're having fun along with buffers based onto a 0.1 M solution of sodium phosphate at pH7.0. Into this system, there are three of pK A s as: 12.7, 7.21 and 2.12.
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