Award-Winning Organic Chemistry Tutors
serving St. Louis, MO

Reaction mechanisms become manageable once a student can track electron movement with confidence, and that's exactly where Jacob starts — arrow-pushing fundamentals before diving into substitution, elimination, and carbonyl chemistry. His biochemistry focus at Missouri State meant he spent serious time with organic transformations that show up in metabolic pathways, giving him a practical lens most tutors lack.

I am excited to help anyone who might need it!

Reaction mechanisms are the language of organic chemistry, and Austin learned to speak it fluently through his chemical engineering coursework, where understanding molecular behavior at the functional-group level was essential. He teaches students to recognize nucleophiles, electrophiles, and leaving groups as characters in a story rather than arrows to memorize. That pattern-recognition approach turns synthesis problems from intimidating puzzles into logical sequences.

I'm a current medical student at VCU School of Medicine, and a graduate of Johns Hopkins University. I received my Bachelor of Science in Molecular and Cellular Biology. I've had the pleasure of tutoring a diverse range of students for 5 years; while I tutor a broad set of subjects, I'm most passionate about biology, psychology, and chemistry. I'm a big proponent of ensuring understanding over memorization and teaching concepts that last for years to come (particularly for other students interested in medicine!) In my free time, I love to write poetry, edit essays, and gush about game writing with friends.

Working in a cancer biology research lab means Yasheen encounters the organic chemistry behind drug design and molecular signaling every day — not as textbook problems, but as real questions about how functional groups determine a molecule's behavior in living systems. She connects that bench-level intuition to the arrow-pushing, stereochemistry, and carbonyl reactivity students need to master in their orgo courses. Rated 5.0 by students.

Penn's pre-health track put Brittany through rigorous chemistry coursework alongside her psychology degree, and she spent her undergraduate years tutoring General Chemistry I and II at the university's Tutoring Center — building the kind of fluency with reaction fundamentals that carries directly into organic mechanisms. She approaches topics like nucleophilic substitution and carbonyl reactivity by connecting them back to the foundational principles of electron behavior and molecular structure, making each new reaction type feel like an extension of something students already know.

Jonathan's human biology degree and pre-med track at Cornell meant organic chemistry wasn't just a prerequisite — it was the course that connected molecular structure to everything he'd later study in physiology and biochemistry. He tackles synthesis problems and spectroscopy interpretation by linking functional group behavior back to biological relevance, which gives students a reason to care about each mechanism. Rated 4.9 by students.

Reaction mechanisms are the language of organic chemistry — if you can't follow electron movement through a nucleophilic substitution or an elimination, every new reaction feels like something to memorize from scratch. Cassandra teaches students to recognize the patterns that repeat across seemingly different reactions: leaving group quality, steric effects, acid-base behavior. That pattern-recognition approach, sharpened by her biology and biochemistry background, turns a notoriously overwhelming course into something students can actually reason through.

Reaction mechanisms click once you stop memorizing arrow-pushing patterns and start understanding why electrons move the way they do — nucleophilicity, sterics, leaving group stability. Mitchell's neuroscience degree required extensive organic chemistry coursework, and he breaks down everything from substitution and elimination reactions to carbonyl chemistry by connecting each mechanism to the electronic principles driving it.

Jacob lists organic chemistry among his favorite subjects to teach, and his economics-trained habit of tracing systems through chains of cause and effect gives him a structured way to walk through multi-step mechanisms — particularly carbonyl chemistry and aromatic substitution patterns. He approaches each reaction type by building the logic from scratch: what's electron-rich, what's electron-poor, and why that determines everything. Rated 5.0 by students.

Most organic chemistry struggles come down to not recognizing patterns — why a nucleophile attacks here and not there, or how electron-pushing arrows predict a product. Eric's graduate training in chemistry means he teaches reaction mechanisms as a connected framework of electronic and steric principles rather than a list of isolated reactions. Students rated him 5.0.

Reaction mechanisms are essentially stories told with curved arrows, and the trick is learning to read them rather than memorize hundreds individually. Mark approaches organic chemistry by teaching students to recognize patterns — nucleophilic attacks, leaving group stability, steric effects — so they can predict products on reactions they've never seen before. His chemistry coursework at Notre Dame keeps these concepts fresh and grounded in real molecular behavior.

Reaction mechanisms are the core of organic chemistry, and most students struggle because they try to memorize arrow-pushing patterns instead of understanding why electrons move where they do. Jamie has tutored organic chemistry extensively alongside his pre-med and medical coursework, and he teaches students to read a mechanism the way you'd read a sentence — identifying the nucleophile, the electrophile, and the driving force before ever drawing an arrow.

Max spent much of high school independently pursuing organic chemistry through coursework and projects well beyond what was required — the kind of deep, self-driven study that builds real fluency with reaction types and synthesis logic. His chemistry degree from MIT and mathematical instincts mean he approaches problems like retrosynthetic analysis and multi-step mechanism design as structured puzzles, breaking each one into clear decision points. Rated 5.0 by students.

Between his biochemistry degree and his current pharmacy doctoral work at VCU, Joel has run through organic chemistry from both the academic and applied sides — understanding how functional group reactivity and stereochemistry translate into real drug design and pharmacological mechanisms. He's also taught university chemistry courses as adjunct faculty, so he knows how to break down multi-step synthesis problems and spectroscopy interpretation at the pace a student actually needs. Rated 5.0 by students.