Award-Winning Organic Chemistry Tutors
serving Nashville, TN

I am a freshman at Vanderbilt University studying biochemistry and involved in analytical chemistry research. Despite my studies being very science oriented, I also enjoy studying English and the humanities. I'd be happy to tutor you in any of these areas!

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.

Reaction mechanisms are the language of organic chemistry, and Kathleen reads them fluently. She completed her undergraduate Chemistry degree at the University of Arkansas and went on to apply organic principles daily during her Vanderbilt Ph.D. research, where understanding molecular structure and reactivity was essential to her lab work. She walks students through arrow-pushing, stereochemistry, and synthesis design by connecting each reaction type to a clear underlying logic.

Reaction mechanisms are the backbone of organic chemistry, and most students struggle because they try to memorize arrow-pushing patterns without understanding electron density or orbital interactions. Fay's biochemistry background means she approaches orgo from a structural and energetic perspective — explaining why an E2 elimination is favored over SN1, not just that it is.

Pre-med coursework in psychology and biology gave Kristen a biomolecular entry point into organic chemistry — she learned reaction mechanisms through the lens of how drugs bind receptors and how metabolic pathways depend on functional group transformations. She tackles arrow-pushing by walking students through the "why" behind electron movement, connecting nucleophilicity and leaving group ability to the biological molecules that make those concepts tangible.

Having taught General Chemistry, Organic Chemistry, and GOB courses for health professions repeatedly at the college level, Jeremy approaches reaction mechanisms as skills to be practiced — not facts to be memorized. His PhD in Chemistry from Yale means he can trace arrow-pushing, stereochemical analysis, and multi-step synthesis all the way down to first principles, then rebuild them at whatever level a student needs. He holds a 4.6 rating.

Surviving organic chemistry as a chemistry major and then revisiting it for dental school admissions gave Jackson two passes through reaction mechanisms, stereochemistry, and spectroscopy interpretation. That repetition means he knows exactly where students get lost — arrow-pushing notation, carbonyl chemistry, substitution vs. elimination — and can walk through each step without skipping the reasoning.

I am a chemistry tutor with a solid academic and teaching background, possessing more than seven years of experience in chemistry. Being a tutor is an exciting interaction surpassing anything else I have experienced. I want to continue tutoring because I can positively influence students to reach their full potential academically. Enabling students to understand the basic knowledge and skills they may use for the rest of their lives is mightily rewarding. I have had a tremendously positive experience of both high school and college education. I received a chemistry bachelor's degree at the Cross River University of Technology, Nigeria, and a master's degree in chemistry at East Tennessee State University, TN. As a high school classroom teacher, and a graduate assistant, I taught a Chemistry course and instructed Organic Chemistry laboratory sessions, respectively. These teaching assignments have kindled positive and gratifying responses. The work of Howard Gardner has influenced my learning style. He theorized that we have many kinds of intelligence and that everyone has the potential to be brilliant but tends to express it uniquely. Therefore, all students have a unique learning style that is suitable for them. As a tutor, I can meet my students' academic needs provided I know their right learning style. Outside teaching, I volunteer in my local church youth weekly program to set up the gym so that the youths could have some fun games before listening to Bible-based teaching. I believe the spiritual well-being of an individual is just as important as their academic success. Volunteering my time to something that makes young people spiritually and mentally fit is fulfilling. Having decided to teach, I look forward to working as a tutor. It will be an honor to make a real difference in the life of those I tutor.

Reaction mechanisms are the backbone of organic chemistry, and most students struggle not because the material is impossibly hard but because they try to memorize hundreds of reactions instead of recognizing patterns. Manpinder approaches orgo by teaching students to trace electron movement through arrow-pushing — once that skill clicks, predicting products for substitution, elimination, and addition reactions becomes systematic rather than overwhelming.

Reaction mechanisms are the language of organic chemistry, and Jon spent his Master's work at Princeton immersed in that language daily. He unpacks arrow-pushing, stereochemistry, and functional group reactivity by tying each mechanism back to the electron behavior driving it, so students build intuition instead of relying on rote memorization. His TA students at Princeton gave him reviews strong enough to earn a teaching award — a good sign for anyone staring down a semester of orgo.

Currently majoring in chemistry at MIT, Nicholas is immersed in the reaction logic and electron-pushing that organic chemistry demands — and he's learning it at a program known for its rigorous mechanistic approach. He breaks down topics like nucleophilic additions and stereochemical outcomes by connecting them to the underlying thermodynamic and kinetic reasoning, making unfamiliar transformations feel predictable rather than random. Rated 5.0 by students.

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.

Siddharth's biology degree means he first encountered organic chemistry through the lens of biomolecules — amino acid reactivity, lipid structures, and the functional group behavior that drives metabolic pathways. That biological framing gives him a practical way to teach arrow-pushing and reaction classifications, connecting each mechanism to molecules students can visualize rather than treating them as abstract exercises.

Having fought through orgo on the path to a 36 ACT and a biology degree — with MCAT prep sharpening every mechanism further — Aleeza knows exactly where students get tripped up on topics like carbonyl additions and substitution-vs-elimination decision-making. She teaches reaction patterns by connecting them back to the biological molecules they show up in, which makes the logic behind electron flow feel purposeful rather than abstract. Rated 4.9 by students.

Biochemistry majors don't just pass organic chemistry — they keep using it, which means Addison is building on reaction mechanisms and functional group behavior in courses well beyond the introductory sequence at Rice. That ongoing exposure to carbonyl chemistry, stereochemistry, and arrow-pushing in biological contexts gives her a practical fluency that makes tutoring sessions feel less like reviewing old notes and more like working through the material with someone who still thinks in it daily.

Reaction mechanisms are the language of organic chemistry, and Jhonatan treats them that way — teaching students to read electron flow through arrow-pushing until substitution, elimination, and addition reactions feel like variations on a theme rather than isolated procedures to memorize. His biochemistry expertise is especially useful when carbonyl chemistry and amino acid reactivity come into play. He holds a 5.0 client rating.

Four years of tutoring organic chemistry at Yale — while simultaneously doing pre-med coursework — gave Marcus a sharp sense of where students get stuck, particularly with carbonyl reactivity and multi-step synthesis planning. His current research at the Hospital for Special Surgery keeps him actively applying these concepts, so he teaches functional group transformations as interconnected tools rather than an isolated reaction catalog.

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.

Reaction mechanisms are the heart of organic chemistry, and they only make sense when a student can track electron movement and predict how functional groups behave. Malcolm is studying biochemistry and cell biology at Rice, where organic chemistry is foundational — he knows which arrow-pushing patterns show up repeatedly and teaches students to recognize them instead of memorizing hundreds of individual reactions.

Having completed both semesters of organic chemistry at the University of Michigan — on top of AP Chemistry before that — Ajay knows exactly where students get stuck, whether it's arrow-pushing in reaction mechanisms or keeping substitution and elimination pathways straight. He teaches students to recognize electron behavior patterns so new reactions feel predictable instead of random.