Map: Organic Chemistry (Bruice)
- Page ID
- 13803
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)This is a textbook map of the Bruice's famous "Organic Chemistry" textbook. It is not a copy of the original textbook, but is mapped to content on the ChemWiki to simulate it.
Front Matter
- 1: Electronic Structure and Bonding (Acids and Bases)
- 2: An Introduction to Organic Compounds- Nomenclature, Physical Properties, and Representation of Structure
- 3: Alkenes- Structure, Nomenclature, and an Introduction to Reactivity • Thermodynamics and Kinetics
- 4: The Reactions of Alkenes
- 5: Stereochemistry- The Arrangement of Atoms in Space; The Stereochemistry of Addition Reactions
- 6: The Reactions of Alkynes- An Introduction to Multistep Synthesis
- 7: Delocalized Electrons and Their Effect on Stability, Reactivity, and pKa (More About Molecular Orbital Theory)
- 8: Substitution Reactions of Alkyl Halides
- 9: Elimination Reactions of Alkyl Halides (Competition between Substitution and Elimination)
- 10: Reactions of Alcohols, Ethers, Epoxides, Amine, and Sulfur- Containing Compounds
- 11: Organometallic Compounds
- 12: Radicals (Reactions of Alkanes)
- 13: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet/Visible Spectroscopy
14: NMR Spectroscopy
- 15: Aromaticity (Reactions of Benzene)
- 16: Reactions of Substituted Benzenes
- 17: Carbonyl Compounds I- Reactions of Carboxylic Acids and Carboxylic Derivatives
- 18: Carbonyl Compounds II- Reactions of Aldehydes and Ketones • More Reactions of Carboxylic Acid Derivatives • Reactions of α, β- Unsaturated Carbonyl Compounds
- 19: Carbonyl Compounds III- Reactions at the α- Carbon
- 20: More About Oxidation-Reduction Reactions
- 21: More About Amines (Heterocylic Compounds)
- 22: The Organic Chemistry of Carbohydrates
- 23: The Organic Chemistry of Amino Acids, Peptides, and Proteins
- 24: Catalysis
- 25: Compounds Derived from Vitamins
- 26: The Organic Chemistry of Metabolic Pathways
- 27: The Organic Chemistry of Lipids
- 28: The Chemistry of Nucleic Acids
- 29: Synthetic Polymers
- 30: Pericyclic Reactions
- 31: The Organic Chemistry of Drugs- Discovery and Design
Back Matter