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Turn your organic chemistry notes into DAT flashcards

Ready-made decks rarely match your course or prep book. Upload your own material and get flashcards that cover exactly what you are studying.

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Why build your own organic chemistry DAT flashcards

Ready-made decks rarely follow your professor's reaction order or the chapters in your prep book, which is why many DAT candidates end up rebuilding their own organic chemistry DAT flashcards by hand. That work takes hours that could go toward practice questions.

  • Mechanism cards that ask why a step happens, not just what it is
  • Reagent and reaction cards grouped by functional group
  • Stereochemistry cards covering R/S assignment and inversion
  • Spectroscopy cards for IR and NMR patterns you need to recognize
Example organic chemistry DAT flashcards
Why does SN2 substitution invert the configuration of a stereocenter?The nucleophile attacks from the side opposite the leaving group in a single concerted step, so the stereocenter flips like an umbrella in wind.
Which is more acidic, ethanol or phenol?Phenol, because its conjugate base is resonance-stabilized as the negative charge delocalizes into the aromatic ring.
What is the hybridization of the carbonyl carbon?sp2, with trigonal planar geometry and bond angles near 120 degrees, leaving one unhybridized p orbital to form the pi bond.
Why do tertiary alkyl halides favor E1 and SN1 over SN2?A tertiary carbocation is relatively stable, and the crowded carbon blocks the backside attack that SN2 requires.
Where does a saturated ketone C=O stretch appear in an IR spectrum?Strong absorption near 1715 cm-1, shifting lower when the carbonyl is conjugated with a double bond or aromatic ring.
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Built from your material

Upload PDFs, slides, typed notes or photos of pages, and get flashcards drawn from your own reaction lists and lecture content.

Spaced repetition

Cards you miss come back sooner, and the ones you know are spaced further apart, so review time goes to the material you are weakest on.

Export when you need it

Study in the browser on the free plan. Plus adds PDF, DOCX, Anki and CSV export for printing or moving cards into another app.

How it works

Upload your notes

Add a PDF, DOCX, PPTX, text file or photo of a page from your organic chemistry course or DAT prep book.

Generate flashcards

DeckOwl reads the text and creates question and answer cards covering mechanisms, reactions, stereochemistry and spectroscopy.

Study on a schedule

Review the deck in the browser. Spaced repetition brings back the cards you struggle with at the right time.

DeckOwl starts from the material you already have. Upload your lecture slides, notes or a scanned page of mechanisms, and it generates cards that follow your course's wording and emphasis, so the deck matches what you will see on the exam.

Spaced repetition then handles the review schedule. Cards you miss come back sooner, which helps with the high volume of reactions, reagents and functional group facts the DAT expects you to recall quickly.

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Frequently asked questions

How many organic chemistry DAT flashcards should I review each day?

There is no fixed number that works for everyone. A daily set you can finish consistently, with spaced repetition deciding what returns, usually beats a large batch you cannot keep up with.

Which organic chemistry topics should DAT flashcards cover?

Focus on reaction mechanisms, functional group reactivity, stereochemistry, acid-base trends and IR and NMR interpretation. Generating cards from your own notes keeps the deck aligned with the topics your course actually taught.

Can I export my flashcards to Anki or print them?

Export to Anki, CSV, PDF and DOCX is included in the Plus plan at $39 per year or $7.99 per month. The free plan lets you study in the browser with 3 generations per month.

Do I need a credit card to start?

No. You can start on the free plan without a credit card, and students can get 40% off a paid plan with a school email.

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