Textbook Map: Brown/Foote/Iverson/Anslyn
- Page ID
- 7879
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)- Covalent Bonding and Shapes of Molecules.
- Alkanes and Cycloalkanes.
- Stereochemistry and Chirality.
- Acids and Bases.
- Alkenes.
- Reactions of Alkenes.
- 6.1 Reactions of Alkenes— An Overview
- 6.2 Organic Reactions Involving Reactive Intermediates
- 6.3 Electrophilic Additions
- 6.4 Hydroboration-Oxidation
- 6.5 Oxidation How To Write a Balanced Half-Reaction
- 6.6 Reduction
- 6.7 Molecules Containing Chiral Centers as Reactants or Products
- Alkynes.
- Haloalkanes, Halogenation, and Radical Reactions.
- Nucleophilic Substitution and B-Elimination.
- Alcohols.
- Ethers, Sulfides, and Epoxides.
- Infrared Spectroscopy.
- Nuclear Magnetic Resonance Spectroscopy.
- Mass Spectrometry.
- Introduction to Organometallic Compounds.
- Aldehydes and Ketones.
- Carboxylic Acids.
- Functional Derivatives of Carboxylic Acids.
- Enolate Anions and Enamines.
- Dienes, Conjugated Systems, and Pericyclic Reactions.
- Benzene and the Concept of Aromaticity.
- Reactions of Benzene and Its Derivatives.
- Amines.
- Catalytic Carbon–Carbon Bond Formation.
- Carbohydrates.
- Lipids.
- Amino Acids and Proteins.
- Nucleic Acids.
- Organic Polymer Chemistry.
Appendices:
- Thermodynamics and the Equilibrium Constant.
- Major Classes of Organic Acids.
- Bond Dissociation Enthalpies.
- Characteristic 1H-NMR Chemical Shifts.
- Characteristic 13C Chemical Shifts.
- Characteristic IR Absorption Frequencies.
- Electrostatic Potential Maps.
- Summary of Stereochemical Terms.
- Summary of the Rules of Nomenclature.
- Common Mistakes in Arrow Pushing.
- Organic Chemistry Roadmaps