- 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
Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)
A type of radioactive decay in which an atomic nucleus emits an alpha particle and thereby transforms (or “decays”) into an atom with a mass number 4 less and atomic number 2 less. (Section 21.1)
One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)
Energetic electrons emitted from the nucleus, symbol 0-1e or b-. (Section 21.1)
bonding molecular orbital.
A molecular orbital that is of lower energy and greater stability than the atomic orbitals from which it was formed. (10.6)
A binary compound of carbon with a metal or metalloid. (Section 22.9)
Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.
A unit of measure fordipole moments, where 1 debye = 10-18 esu×cm.
A technique for separating amino acids from each other based on a difference in pI values.
energy of activation
In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.
A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.
Ground-state electron confi guration
The lowest-energy electron confi guration for an atom or molecule.
Heterolytic bond cleavage
Cleavage of a bond so that one fragment retains both electrons and the other retains none.
A system for naming organic compounds.
A molecule that possesses a nonzero dipole moment. (Section 8.4)
The determination of the presence or absence of a particular substance in a mixture. (Section 17.7)
An intermediate that has both a negative charge and an unpaired electron.
retention of configuration
During a reaction, when the configuration of a chirality center remains unchanged.
The amount of time required for a compound to exit from a gas chromatograph.
A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.
Having trouble accessing your account? Let us help you, contact support at +1(510) 944-1054 or firstname.lastname@example.org
Forgot password? Reset it here