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Practice organic chemistry with a quiz app made from your notes

Upload your lecture slides, textbook PDF or typed notes and get multiple-choice, true/false or open questions on mechanisms, stereochemistry and reactions, each with an explanation.

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Why practice quizzes work for organic chemistry

Organic chemistry rewards questions that ask why a reaction goes one way and not another. An organic chemistry quiz app that builds questions from your own lecture slides or textbook PDF lets you test the exact mechanisms your course covers, including SN1 versus SN2 conditions and stereochemistry.

  • Questions are generated from your own material, not a generic question bank.
  • Explanations tell you why the right answer is right, which matters most in mechanism problems.
  • Multiple choice, true/false and open questions cover recall and reasoning.
  • Free plan includes 3 generations per month with browser study and no credit card needed.
Example organic chemistry quiz questions
Which is more acidic, ethanol or phenol?Phenol. Its conjugate base is stabilized by resonance into the aromatic ring, while ethoxide has no comparable stabilization.
True or false: E2 elimination requires the leaving group and a beta hydrogen to be anti-periplanar.True. The two groups must align at 180 degrees so their orbitals overlap during the concerted step.
In HBr addition to propene, why does the proton add to the terminal carbon?It follows Markovnikov's rule, giving the more stable secondary carbocation as the intermediate instead of a primary one.
What is the maximum number of stereoisomers for a molecule with two stereocenters?Four, since 2 to the power of n gives up to 2^n stereoisomers. Meso compounds can reduce the number of distinct ones.
Why does an aldehyde react more readily with nucleophiles than a ketone does?The aldehyde carbonyl carbon has less electron donation from alkyl groups and less steric hindrance, so it is more electrophilic.
Generate the full set

Questions from your own material

Reaction mechanisms, stereochemistry and named reactions come from the chapters and slides you upload, so the quiz tracks what your course actually covers.

Three question types

Multiple choice, true/false and open questions, each with an explanation that shows why the correct arrow-pushing step or product is right.

Study now or export later

Study in the browser on the free plan. Paid plans add PDF and DOCX export, and Pro adds QTI 2.1 and Moodle XML for course platforms.

How it works

Upload your material

Add a PDF, DOCX, PPTX, plain text notes or a photo of a textbook page. Photos are read with text recognition.

Choose a question type

Pick multiple choice, true/false or open questions. Open questions are useful for explaining why a product forms.

Answer and review

Work through the quiz, read the explanation for each answer and return to the questions you missed.

Each question comes with an explanation, so a wrong answer becomes a lesson about electron movement, leaving groups or steric effects. Working through short quizzes after each chapter tends to show gaps sooner than rereading a long chapter.

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Frequently asked questions

How should I study organic chemistry reaction mechanisms?

Draw each arrow-pushing step yourself before checking the answer. Then quiz yourself on the conditions that favor SN1 versus SN2 or E1 versus E2, not only on which product forms.

Should I memorize reactions or learn the patterns behind them?

Learn the patterns, such as nucleophile strength, leaving group ability and solvent effects, because they explain most reactions you will meet on exams. Open questions that ask why a product forms test this better than memorized lists.

Can I export my organic chemistry quizzes to my course platform?

Yes, QTI 2.1 and Moodle XML export are included on the Pro plan. PDF and DOCX export are available on Plus, and the free plan is for studying in the browser.

Is there a free plan to try it first?

Yes, the free plan includes 3 generations per month and no credit card is needed to start. Plus is $39/year or $7.99/month, and students get 40% off with a school email.

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Keep exploring the topic

Review the main ideas visually or practice recalling them.