Award-Winning Organic Chemistry Tutors
serving Barnstable, MA

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.

Teaching two Chemistry 101 lab sections gave Davis hands-on experience explaining reaction mechanisms, functional group behavior, and electron-pushing arrows to students encountering them for the first time. He approaches organic chemistry as a language of patterns — once students learn to read electron density and leaving-group tendencies, synthesis problems become far more manageable.

Nicole's graduate work in Cellular and Molecular Biology at Duke means she's constantly tracing biochemical pathways back to the organic reactions that drive them — carbonyl additions, acyl substitutions, the functional group chemistry that makes metabolism possible. That daily immersion gives her a way of teaching arrow-pushing and reaction prediction that's rooted in seeing these mechanisms actually matter, not just memorizing reagent tables. Rated 4.9 by students.

I am also a first year medical student at the Tufts University School of Medicine in Boston. I have extensive experience with premedical classes and have taken and tutored the MCAT exam. I placed in the 97th percentile of the MCAT exam and I understand what the test takers want students to know and how to bridge the gap between knowing the material and doing well on the test. I am always excited when a student finally has that "ah-ha" moment and declares that they now can see how all of these seemingly separate scientific topics are actually all related. The MCAT no longer seems scary, but turns into a means of truly learning this material and providing a strong foundation for the future.

Reaction mechanisms start making sense when you can trace electron movement step by step — arrow pushing, nucleophilic attacks, leaving groups. Will's pre-med concentration at Boston University meant semesters of organic chemistry where he learned to connect functional group behavior to real biochemical pathways. Rated 5.0 by students, he breaks down synthesis problems into logical chains rather than memorization marathons.

Reaction mechanisms are the language of organic chemistry, and Marc learned that language thoroughly during his biochemistry degree, where every biosynthetic pathway demanded fluency with nucleophilic attacks, stereochemistry, and electron-pushing. He walks through each mechanism step by step, connecting arrow-pushing to the actual energetics driving the reaction.

Reaction mechanisms are the language of organic chemistry, and Michael learned to speak it fluently during his Chemistry & Chemical Biology program at Cornell. He teaches students to trace electron movement through substitution, elimination, and addition reactions so they can predict products instead of relying on memorized shortcuts.

Tufts Biomedical Science coursework gave Sarah repeated exposure to organic chemistry concepts well beyond a single semester — she's traced reaction mechanisms through pharmacology, biochemistry, and molecular biology, which means she knows how carbonyl reactivity and functional group transformations actually show up downstream. She breaks multi-step synthesis problems into decision points: what's the nucleophile, what's leaving, and what drives the reaction forward. Rated 5.0 by students.

Chemical engineering at Columbia and MIT means Kelsey has worked through organic chemistry from both the academic and applied sides — synthesis design, reaction kinetics, and process-level thinking about how functional group transformations scale beyond a single flask. She digs into the thermodynamic and kinetic reasoning behind selectivity questions, like why one reaction pathway dominates under specific conditions, giving students a problem-solving framework they can carry into exams. Rated 4.9 by students.

Reaction mechanisms are the backbone of organic chemistry, and they stop being intimidating once you learn to read electron movement like a story rather than memorize arrow-pushing patterns. Vaibhav's cellular and molecular biology program at Pitt required extensive organic chemistry coursework, so he teaches substitution, elimination, and addition reactions through the lens of someone who's applied them in biochemical contexts. He unpacks each mechanism by starting with why electrons move, then building to predicting products.

I'm well versed in areas of General Chemistry, as well as Algebra and Geometry.

Reaction mechanisms are the backbone of organic chemistry, and Claire — who earned her chemistry degree from Amherst — teaches them by tracing electron movement through each step of substitution, elimination, and addition reactions. Instead of memorizing hundreds of individual reactions, her students learn to predict products by understanding nucleophilicity, sterics, and leaving group ability. That pattern-recognition approach is what got her a 5.0 rating.

Pursuing biochemistry at Tufts while prepping for medical school means Suraj has worked through organic chemistry with the kind of rigor that comes from needing every mechanism to stick — not just for one exam, but for MCAT prep and upper-level biochemistry courses that build directly on it. He zeroes in on where a student's reasoning breaks down mid-mechanism, whether it's misidentifying the nucleophile in an addition-elimination or losing track of stereochemistry through a multi-step synthesis, and rebuilds the logic from that exact point. Rated 5.0 by students.

I am currently a Ph.D. student at Harvard University in the department of Chemistry and Chemical Biology.

I am a graduate of Boston University (BU) as of 2012, and I recently graduated from Tufts University in 2014. I have received my Bachelors of Science in Biomedical Engineering from BU, and I have earned my Masters of Science degree in the same field at Tufts. I currently work as a research scientist in Cambridge studying therapies for Alzheimer's and Parkinson's Disease. My tutoring experience stems from my involvement in the National Honor Society at Xaverian Brothers High School where I tutored Freshman and Sophomore classes in our mathematics and science, specifically Algebra, Calculus and Biology. Furthermore, after being inducted in the Tau Beta Pi Engineering Honor Society at BU, I led tutoring sessions specifically geared to Engineering principles such as mechanics, physics, and mathematics. As an engineer, my favorite subjects to study are High School to College Mathematics as well as the Sciences (Physics, Chemisty, Biology) because it gives the mind a great workout! I am a generally upbeat and motivated individual which is essentially translated to my tutoring strategies; if you can somehow make the subject engaging, the more chances the student will want to learn the material! I enjoy that "A-ha!" moment when the student fully and finally understands a concept! In my spare time, I am a competitive ballroom dancer, theater aficionado and a scientific researcher in biomedical engineering!

I am an avid skier and outdoorswoman, and a passionate fan of Boston sports. As a tutor, I offer a broad range of scientific subjects, including Physics, Chemistry and Biology, and I am particularly passionate about Biochemistry and Microbiology. I also offer and enjoy test prep, including the SAT and independent school entrance exams such as the ISEE and SSAT. As an educator, I am passionate about helping every student, because I believe that everyone has the potential to succeed in Science and excel on standardized tests. I love the subjects I tutor and I strive to help my students appreciate the value of knowledge so they understand not only the material, but why it is relevant and important in their lives.

I am currently a second year medical student at Tufts University. I was a tutor for fpur years at Brigham Young University, and I love helping people learn! I tutor Economics, Math and all the basic sciences. I really enjoy tutoring these subjects because my students and I work together to understand the principles underlying the problems, which helps us remember everything better and makes studying more enjoyable. My tutoring theory is that students either know the answer or know how to find it, and together we can make that happen.

I have always enjoyed teaching even when I was in grade school helping my friends with their homework. I live for that 'aha!' moment with a student! I have tutored off and on for the past 10 years both as a tutor in math and chemistry and later as a teaching assistant in chemistry during graduate school. I love to meet students where they are and build from there. We break complex concepts into digestible pieces to build upon where your understanding already is.

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.

As an MD/PhD student at Northwestern doing doctoral research in organic synthesis, Austin lives in the world of reaction design — figuring out which bonds to form, which protecting groups to use, and why one retrosynthetic route beats another. That daily immersion means he teaches mechanisms and stereochemistry with the fluency of someone who actually builds molecules, not just someone who once passed the course.

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 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.

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.

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 Josef teaches students to read them — arrow pushing, stereochemistry, and functional group reactivity — rather than memorize hundreds of individual reactions. His biochemistry focus at Cornell means he can connect orgo concepts like nucleophilic substitution and carbonyl chemistry directly to biological molecules students will encounter later.

Reaction mechanisms, stereochemistry, and functional group transformations all require a kind of visual logic that's unlike anything in general chemistry. Greg's chemical engineering background at Vanderbilt gave him deep exposure to organic reaction pathways, and he teaches students to trace electron movement step by step so they can predict products instead of relying on memorization.