Organic Reactions
Every reaction you meet in Organic Chemistry I and II — reagents, mechanism, and what the product actually looks like.
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229 reactions and 655 glossary terms, written to be understood at 1am the night before the exam.
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Everything is grouped the way a course is, so you can find what you are being examined on instead of scrolling a blog.
Every reaction you meet in Organic Chemistry I and II — reagents, mechanism, and what the product actually looks like.
The chemistry of life — amino acids, proteins, enzymes, membranes and the molecules that carry oxygen around your body.
The groundwork every chemistry course is built on — structure, charge, stereochemistry and how to read a mechanism.
Reading the instruments — NMR, IR and UV-Vis, plus how to turn a spectrum into a structure.
The tables you keep re-searching for — readable on a phone, sortable on a laptop.
655 terms, searchable, each with a definition and a worked explanation.
Codes, side-chain classes and pKa values in one sortable table.
The values that decide almost every acid-base question you will be asked.
Structure, IUPAC suffix and prefix for all 18 groups.
What each reagent does, what it works on, and the trap that goes with it.
Quick self-test on mechanisms, reagents and nomenclature.
The ones students look up most.
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EnantiomersDiastereomersSummary: Enantiomers vs. Diastereomers
With E1 and E2 mechanisms we have already met, but let’s compare them now. Both are elimination reactions. When alkyl ha
Formation of the carbocationCarbocationsCarbocation stability
Stereochemistry of the dienophileStereochemistry of dieneEndo ruleWhen “endo” and “exo” products are possible, the “endo