- Chapter 1: Covalent Bonding and Shapes of Molecules
- Chapter 10: Alcohols
- Chapter 11: Ethers, Epoxides, and Sulfides
- Chapter 12: Infrared Spectroscopy
- Chapter 13: Nuclear Magnetic Resonance Spectroscopy
- Chapter 14: Mass Spectrometry
- Chapter 15: An Introduction to Organometallic Compounds
- Chapter 16: Aldehydes and Ketones
- Chapter 17: Carboxylic Acids
- Chapter 18: Functional Derivatives of Carboxylic Acids
- Chapter 19: Enolate Anions and Enamines
- Chapter 2: Constitutional Isomerism in Alkanes
- Chapter 20: Dienes, Conjugated Systems, and Pericyclic Reactions
- Chapter 21: Benzene and the Concept of Aromaticity
- Chapter 22: Reactions of Benzene and Its Derivatives
- Chapter 23: Amines
- Chapter 24: Catalytic Carbon-Carbon Bond Formation
- Chapter 3: Stereoisomerism and Chirality
- Chapter 4: Acids and Bases
- Chapter 5: Structure of Alkenes
- Chapter 6: Electrophilic Additions
- Chapter 7: Alkynes
- Chapter 8: Haloalkanes, Halogenation, and Radical Reactions
- Chapter 9: Nucleophilic Substitution and b-Elimination
Organic Chemistry 7th Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 7th Edition
An amine in which nitrogen is bonded to one or more aryl groups.
beta (b) pleated sheet
For proteins, a feature of secondary structure that forms when two or more protein chains line up side-by-side.
Charles’ and Gay-Lussac’s law.
See Charles’ law.
The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)
A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond
Saturated hydrocarbons of general formula CnH2n in which the carbon atoms form a closed ring. (Section 24.2)
A measure of a solvent’s ability to insulate opposite charges from one another
A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)
Enthalpy change, DH
The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram
A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.
The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)
A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)
A compound composed of cations and anions. (Section 2.7)
The absolute temperature scale; the SI unit for temperature is the kelvin. Zero on the Kelvin scale corresponds to -273.15 °C. (Section 1.4)
A spectrum that contains radiation at only certain specific wavelengths. (Section 6.3)
A substance produced in a chemical reaction; it appears to the right of the arrow in a chemical equation. (Section 3.1)
A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.
A method for preparing substituted amines by treating an aldehyde or ketone with an amine in the presence of a reducing agent
A compound that can be used to achieve the resolution of enantiomers.
secondary alkyl halide
An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.