Organic Chemistry AI
that makes hard problems look obvious

Each request shows the credit cost before you submit, so you can decide. Simple text questions usually cost less, while image-based questions (photos of reactions, mechanisms, or spectra) may cost more because they require extra analysis. If you’re on a plan, your remaining credits update instantly after each run. For the most accurate estimate, check the cost label next to the input box and your credit counter on the page.

Yes—Organic Chemistry AI can explain mechanisms step-by-step (electron flow, intermediates, resonance checks) and help you understand why a reaction gives that product. It’s especially useful for SN1/SN2, E1/E2, additions, carbonyl chemistry, and aromatic substitutions. If your question includes stereochemistry or selectivity, add a note like “major/minor” or “show stereochemistry (R/S, E/Z)” to get the clearest reasoning.

Yes. For synthesis problems, it can propose a route, list reagents, and explain the logic behind each step—especially functional group interconversions and reaction order. For retrosynthesis, it can suggest reasonable disconnections and forward steps. To improve results, include your constraints: number of steps, allowed starting materials, or whether protecting groups are allowed.

It can help interpret common spectroscopy questions, including ¹H NMR (shift, splitting, integration), ¹³C NMR patterns, IR diagnostic peaks, and basic MS fragmentation cues. For best results, paste peak lists (or upload a clear screenshot), and tell it what you need: “assign peaks,” “propose a structure,” or “confirm functional group.” If the spectrum is blurry, type the peak table manually for higher accuracy.