Award-Winning Organic Chemistry Tutors
serving Spokane, WA

Helping students in their education is my passion. I understand how frustrating it is to keep trying on understanding a concept or master a skill without getting a satisfying result. I aim to help students enjoy learning and acquiring knowledge. Always remember that knowledge is power, and nobody can take it from you. I have sufficient tutoring and teaching experience in secondary and post-secondary settings. I worked as a tutor at the University of Wisconsin Oshkosh. I tutored college students different courses in mathematics, physics, biology, chemistry, and psychology. Also, l worked as a graduate teaching assistant at Marquette University. I taught the laboratory part of general chemistry, analytical chemistry, and organic chemistry. Furthermore, l worked as a science teacher at different secondary schools. I taught science for grades 4,5,6, and 8. Also, l taught chemistry for grade 9. When it comes to my education, l have a bachelor degree in biology healthcare science and chemistry biomolecular science (double major). In addition, l have a master's degree in chemistry. I received my undergraduate education at the University of Wisconsin Oshkosh and my graduate education at Marquette University. I tutor for numerous subjects such as algebra, trigonometry, calculus, physics, organic chemistry, analytical chemistry, human anatomy, developmental biology, ecology, and biochemistry. Also, l tutor for the GRE, DAT, TOEFL, and IELTS. My favorite subjects are the math, physics, biology, and chemistry subjects because l, simply, enjoy these fields. My teaching philosophy and tutoring style are based on practicing with various examples. When you are confronted with numerous problems to solve, you become more confident in that subject area. As a result, better performance in quizzes and exams. Outside of academia, learning about other cultures and countries around the world is my interest.

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.

Studying physics with a concentration in chemical principles at Penn means Max encounters organic chemistry from the physical side first — thermodynamics of reaction pathways, orbital interactions driving nucleophilic attacks, and the energy landscapes that determine whether a substitution or elimination wins out. That perspective lets him teach mechanisms by grounding arrow-pushing in the physics of why electrons move, not just where they go.

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!

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.

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.

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.

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.

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.

Reaction mechanisms are the language of organic chemistry, and Amin earned an entire master's degree becoming fluent in them. He teaches students to read electron flow the way you'd read a sentence — identifying nucleophiles, leaving groups, and stereoelectronic effects so that predicting products becomes a reasoning exercise, not a memorization marathon. Rated 4.5 by students.

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.

Studying biochemistry and molecular biology means Raj encountered organic chemistry not as a single course but as the language underlying everything from enzyme kinetics to metabolic pathways — so he teaches functional group reactivity and stereochemistry with that bigger picture always in view. His 5.0 rating and a perfect 36 ACT reflect someone who thinks systematically, which translates directly into how he walks students through multi-step synthesis problems: identify the transformation, trace the electron flow, then confirm the regiochemistry.

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.