Draw the conjugate bases of pyrrole and cyclopentadiene. Explain Why is the sp3 hybridized C―H bond of cyclopentadiene more acidic than the N―H bond of pyrrole?

The explanations are given in the section below

Explanation:

First step:

We need to understand the acid-base equilibrium of the reaction. Bear in mind that the conjugate acid-base pairs are species that differ by one proton. Furthermore, one is a Lewis acid (meaning the ability to protons) and the conjugate base (accepts protons)

A simple conjugate base is obtained by removing one proton from an acid as shown below:

HX ⇄ A⁻ + H⁺

The diagrams are as follows:

i think its 100.

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