Organic chemistry mechanisms are the clearest use case for this method in chemistry. The standard approach is to draw the mechanism on paper rather than only narrating it. For each arrow you draw, state out loud what is moving (electrons), where it is coming from (a lone pair, a pi bond, a sigma bond), and where it is going and why (the electrophilic carbon, the stable leaving group).
If you draw an arrow and cannot explain why the electrons move in that direction, stop. That is the gap. Reread the mechanism in your notes or textbook, paying attention to the electron density logic rather than the arrow pattern. Return to the blank page and redraw from the start.
This is more effective than re-reading mechanisms passively because it forces you to generate the logic rather than recognise it. Recognition fails under exam conditions when the question uses an unfamiliar substrate. Generation transfers to new examples.