Award-Winning Organic Chemistry Tutors
serving Memphis, TN

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 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.

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 Natasha teaches them the way she learned them in her biomolecular engineering program — by tracing electron movement step by step until the logic feels inevitable rather than arbitrary. She digs into arrow-pushing, stereochemistry, and functional group reactivity by asking students to predict products before revealing answers, building real intuition for how molecules behave.

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.

Chemical engineering at Cornell meant Rahul didn't just pass organic chemistry — he applied it daily in reactor design, synthesis planning, and thermodynamic analysis of reaction pathways. That engineering lens gives him a distinctive angle on topics like carbonyl chemistry and stereoselectivity, where he ties mechanism logic back to energy landscapes and kinetic versus thermodynamic control. Rated 4.9 by students.

Reaction mechanisms in organic chemistry reward the same kind of systematic thinking that drives engineering design: track the electrons, identify the functional groups, and predict what happens next. Lee teaches students to read mechanisms as stories with cause and effect — nucleophile attacks electrophile, leaving group departs — instead of memorizing hundreds of individual reactions. His biomedical background adds context for why specific organic reactions matter in drug design and biochemistry.

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.

Studying chemistry at Harvard while preparing for Columbia Medical School means James has worked through organic chemistry from both the academic and pre-med sides — understanding mechanisms deeply enough to satisfy a chemistry major, and efficiently enough to apply them in biochemistry and pharmacology contexts. He's particularly strong at teaching students how to predict reaction outcomes by analyzing charge stability and leaving group trends rather than treating each transformation as a new thing to memorize. Rated 4.9 by students.

Reaction mechanisms become far more intuitive when you understand the electron-level logic behind each arrow push. Andrew earned his biochemistry degree and continues working in biochemical laboratories, so he teaches organic chemistry as a language of molecular behavior — connecting nucleophilic substitutions, elimination pathways, and carbonyl chemistry to the biological contexts where they actually matter.

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 backbone of organic chemistry, and most exam mistakes trace back to shaky arrow-pushing fundamentals. Abhinav teaches students to classify reactions by nucleophile-electrophile interactions first, then layer on stereochemistry and regiochemistry — an approach that turns a seemingly infinite number of reactions into a manageable set of patterns.

Reaction mechanisms are the backbone of organic chemistry, and spotting nucleophilic attacks or predicting stereochemical outcomes requires genuine pattern recognition, not rote memorization. Lauren's chemistry minor at Duke and her hands-on lab research give her a practical fluency with functional group reactivity that she translates into clear, step-by-step reasoning for each mechanism type.

Reaction mechanisms are the backbone of organic chemistry, and learning to predict products means recognizing electron-density patterns, not memorizing hundreds of individual reactions. Alec's approach — honed through years of TA work in Cornell's chemistry department — emphasizes arrow-pushing logic and functional group reactivity so that substitution, elimination, and addition reactions start to feel like variations on a theme rather than separate things to memorize.

Most organic chemistry frustration comes from trying to memorize hundreds of reactions instead of recognizing the handful of electronic patterns — nucleophilic attack, leaving group ability, steric effects — that drive all of them. Garrett teaches students to read arrow-pushing mechanisms as stories about electron movement, which makes predicting products and regiochemistry intuitive. His approach turns reaction maps from overwhelming charts into logical flowcharts.