Organic Chemistry (OpenStax)
- Page ID
- 448507
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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 text continues to meet the scope and sequence of a two-semester organic chemistry course that follows a functional group approach. A highlighted list of changes, along with a detailed table of contents and ancillary descriptions, can be found on the Instructor and Student resources sections of this page. John McMurry decided to publish Organic Chemistry: A Tenth Edition under an open license as a tribute to his son, Peter McMurry, who passed away from cystic fibrosis in December 2019.
- Front Matter
- 1: Structure and Bonding
- 2: Polar Covalent Bonds; Acids and Bases
- 3: Organic Compounds- Alkanes and Their Stereochemistry
- 4: Organic Compounds - Cycloalkanes and their Stereochemistry
- 5: Stereochemistry at Tetrahedral Centers
- 6: An Overview of Organic Reactions
- 7: Alkenes - Structure and Reactivity
- 8: Alkenes - Reactions and Synthesis
- 9: Alkynes - An Introduction to Organic Synthesis
- 10: Organohalides
- 11: Reactions of Alkyl Halides- Nucleophilic Substitutions and Eliminations
- 12: Structure Determination - Mass Spectrometry and Infrared Spectroscopy
- 13: Structure Determination - Nuclear Magnetic Resonance Spectroscopy
- 14: Conjugated Compounds and Ultraviolet Spectroscopy
- 15: Benzene and Aromaticity
- 16: Chemistry of Benzene - Electrophilic Aromatic Substitution
- 17: Alcohols and Phenols
- 18: Ethers and Epoxides; Thiols and Sulfides
- 19: Aldehydes and Ketones- Nucleophilic Addition Reactions
- 20: Carboxylic Acids and Nitriles
- 21: Carboxylic Acid Derivatives- Nucleophilic Acyl Substitution Reactions
- 22: Carbonyl Alpha-Substitution Reactions
- 23: Carbonyl Condensation Reactions
- 24: Amines and Heterocycles
- 25: Biomolecules - Carbohydrates
- 26: Biomolecules- Amino Acids, Peptides, and Proteins
- 27: Biomolecules - Lipids
- 28: Biomolecules - Nucleic Acids
- 29: The Organic Chemistry of Metabolic Pathways
- 30: Orbitals and Organic Chemistry - Pericyclic Reactions
- 31: Synthetic Polymers
- 32: Appendix
- Back Matter