Cyclopentadiene readily undergoes other Diels-Alder reactions with dienophiles such as 1,4-benzoquinone.

However, the most commonly used stable isotope tracers involve relatively light isotopes, which readily undergo fractionation in natural systems.

However, benoxaprofen will not readily undergo oxidative metabolism.

The Schiff base readily undergoes deprotonation in the M intermediate.

The ammonia molecule readily undergoes nitrogen inversion at room temperature; a useful analogy is an umbrella turning itself inside out in a strong wind.

Uracil readily undergoes regular reactions including oxidation, nitration, and alkylation.

Simple ketones and aldehydes readily undergo addition of phosphites at the carbonyl carbon.

Substances that do not readily undergo chemical reactions, such as N2.

This carbocation intermediate can readily undergo rearrangements, which can lead to a complex mixture of products.

Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.