To draw the structure of the modified nucleoside 2',3'-dideoxy-3'-fluorocytidine, start with the regular nucleoside cytidine and make specific substitutions on the ribose ring. Remove both hydroxyl (OH) groups at the 2' and 3' positions, replacing the 3' OH with a fluorine atom. Understanding the chemistry behind these modifications is essential, particularly the role of valence electrons and how they relate to the atoms being replaced. This exercise aims to deepen comprehension of the relationship between chemistry and biology, rather than just memorizing molecular patterns. Focus on grasping the underlying concepts to effectively tackle similar problems in the future.