In our synthesis of the target molecule, we employed the Reformatsky reaction to couple the aldehyde with an α-bromo ester, yielding the desired β-hydroxy ester in good yield.

The Étard reaction selectively oxidizes a benzylic methyl group on an aromatic ring to the corresponding aldehyde using chromyl chloride.

In our lab meeting, we discussed recent improvements in yield for Kulinkovich reactions and planned follow-up experiments.

In the chemistry lab, we observed complex oscillatory patterns in the BZ reactions under a microscope.

During the lecture, the professor demonstrated a colorful BZ reaction that formed spiral patterns.

We investigated the McCormack reaction to synthesize a variety of phospholenium salts from simple 1,3-dienes.

The dermatologist explained that id reactions often appear as itchy rashes distant from the primary infection.

The patient developed an id reaction characterized by widespread eczematous lesions secondary to an inflammatory tinea of the feet.

The synthesis of the alkyl iodide proceeded smoothly via a Finkelstein reaction in acetone.

The chemist explained how a precipitation reaction can drive an equilibrium toward product formation by continuously removing the product as an insoluble solid.