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Turn your ochem notes into MCAT-style practice questions

Upload your organic chemistry notes, slides or PDFs and get multiple-choice, true/false and open questions with a worked explanation for each answer.

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Why generate your own set instead of using a fixed bank

Organic chemistry on the MCAT rewards mechanistic reasoning, so a fixed set of MCAT ochem practice questions goes stale once you have memorized the answers. Ready-made sets rarely match the exact reactions your course covered this week.

Upload lecture slides, textbook excerpts or handwritten notes photographed as pages
Mix multiple choice, true/false and short answer questions in one set
Review explanations that show the mechanism behind each answer
Export to PDF or DOCX on Plus, or to QTI 2.1 and Moodle XML on Pro

Example MCAT ochem practice questions

Which reagent oxidizes a primary alcohol to an aldehyde without further oxidation to a carboxylic acid?PCC (pyridinium chlorochromate) in dichloromethane. Under these anhydrous conditions the aldehyde does not hydrate and get oxidized further.

True or false: an SN2 reaction proceeds with inversion of configuration at the stereocenter.True. The nucleophile attacks from the side opposite the leaving group, flipping the other three substituents like an umbrella in wind.

Which is more acidic, phenol or cyclohexanol?Phenol. Its conjugate base is stabilized by resonance into the aromatic ring, which spreads the negative charge.

Why is SN2 essentially blocked at a tertiary alkyl halide?Three alkyl groups crowd the carbon and sterically hinder the backside approach that SN2 requires.

How many stereoisomers does a molecule with two stereocenters and no internal symmetry have?Four, forming two pairs of enantiomers. A meso form would reduce the count, but without internal symmetry the maximum of 2^2 = 4 applies.

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Built from your material

Questions come from the lectures, textbook chapters and notes you upload, so they match the reactions and mechanisms you are actually covering.

Explanations for every answer

Each question includes a short explanation of why the correct choice works and where the wrong choices go astray.

Export when you need it

Free users study in the browser. Plus adds PDF and DOCX export, and Pro adds QTI 2.1 and Moodle XML for course platforms.

How it works

Upload your notes

Add a PDF, DOCX, PPTX, plain text file or photos of pages. Photos are read with text recognition.

Choose a question type

Pick multiple choice, true/false or short answer, then generate a set from the topics you uploaded.

Practice and review

Work through the questions, read the explanations, and return to the ones you missed.

Generating questions from your own material keeps practice aligned with what you are studying. Upload a chapter on substitution and elimination, and the questions focus on those reactions, solvents and stereochemical outcomes instead of a general mix.

Explanations matter as much as the answer key. Reading why an SN2 product inverts, or why a carbocation rearranges, builds the reasoning MCAT passages test.

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Frequently asked questions

How do I study reaction mechanisms for the MCAT?

Practice drawing the arrow pushing for each mechanism, then predict products from conditions such as solvent, temperature and nucleophile strength. Memorizing reactions without these predictions tends to fail on unfamiliar passages.

Which organic chemistry topics appear most often on the MCAT?

Acid-base behavior, substitution and elimination, carbonyl chemistry and stereochemistry come up frequently in MCAT-style passages. Check the current AAMC content outline for the official scope.

Is the free plan enough to practice?

The free plan includes 3 generations per month and studying in the browser, so you can test the question style before committing. Exports require a paid plan.

Can I export generated questions to a course platform?

Yes. PDF and DOCX export are included with Plus, and QTI 2.1 and Moodle XML export are part of the Pro plan.

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