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Master Organic Chemistry 1

47

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47 skills · 760 questions

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47 core skills 100% total weight

01

Addition to Alkynes and Partial Reductions

02

Catalytic Hydrogenation and Reduction Concepts

03

Electrophilic Addition to Alkenes

04

Halogenation and Halohydrin Formation

05

Hydration Reactions (Acid-Catalyzed, Oxymercuration)

06

Hydroboration–Oxidation

07

Ozonolysis and Oxidative Cleavage of Alkenes

08

Addition to Conjugated Dienes

09

Conjugated Dienes and Allylic Stability

10

Diels–Alder Reaction

11

IUPAC Naming: Alkanes and Cycloalkanes

12

IUPAC Naming: Alkenes Alkynes, Alkyl Halides

13

IUPAC Naming: Functional Group Compounds

14

Common Rearrangements (Hydride/Alkyl Shifts)

15

Curved-Arrow Formalism and Mechanistic Bookkeeping

16

Intermediates: Carbocations, Carbanions, Radicals

17

Kinetics vs Thermodynamics in Product Distributions

18

Leaving Groups and Substrate Effects

19

Reaction Coordinate Diagrams and Transition States

20

Multi-Step Synthesis: Functional Group Interconversions

21

Predicting Major Products: Regioselectivity and Stereoselectivity

22

Purification Basics (Extraction, Recrystallization, Distillation)

23

Reaction Conditions and Reagent Recognition

24

Spectroscopy: IR and 1H NMR Recognition

25

Structure Drawing

26

Radical Addition to Alkenes (HBr/Peroxides)

27

Radical Halogenation: Selectivity and Mechanism

28

Chirality and Stereocenters: Identify and Classify

29

Conformational Analysis: Newman Projections

30

Cyclohexane Conformations: Chair, Axial/Equatorial

31

E/Z and Alkene Stereochemistry

32

Enantiomers, Diastereomers, and Meso Compounds

33

R/S Configuration (CIP Rules)

34

Stereochemical Outcomes in Reactions (Stereo/Regio)

35

Acid–Base Concepts (pKa, Conjugates)

36

Aromaticity Basics (Hückel Rule)

37

Functional Groups: Identification and Properties

38

Hybridization, Bonding, and Molecular Geometry

39

Inductive Effects and Electronegativity Trends

40

Nucleophiles and Electrophiles: Recognizing Reactivity

41

Resonance, Formal Charge, and Stability Trends

42

E1 Reactions and Competing Pathways

43

E2 Reactions: Anti-Periplanar Requirement

44

Elimination Products: Zaitsev vs Hofmann

45

SN1 Reactions: Carbocation Stability, Rearrangements

46

SN1/SN2/E1/E2 Decision Framework

47

SN2 Reactions: Conditions, Stereochemistry, Rate