- Chapter 1:
- Chapter 10:
- Chapter 11:
- Chapter 12:
- Chapter 13:
- Chapter 14:
- Chapter 15:
- Chapter 16:
- Chapter 17:
- Chapter 18:
- Chapter 19:
- Chapter 19.T:
- Chapter 2:
- Chapter 2.T:
- Chapter 20:
- Chapter 21:
- Chapter 22:
- Chapter 23:
- Chapter 24:
- Chapter 25:
- Chapter 26:
- Chapter 27:
- Chapter 28:
- Chapter 3:
- Chapter 4:
- Chapter 5:
- Chapter 6:
- Chapter 7:
- Chapter 8:
- Chapter 9:
Organic Chemistry 7th Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 7th Edition
The addition of H2 across only one face of a p bond.
The process whereby water spontaneously forms low concentrations of H+1aq2 and OH-1aq2 ions by proton transfer from one water molecule to another. (Section 16.3)
A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.
In NMR spectroscopy, protons (or carbon atoms) that occupy identical electronic environments and produce only one signal.
Atoms that lie in the same plane.
coupling (of protons)
A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.
Having the same energy.
Electrons that are spread over a number of atoms in a molecule or a crystal rather than localized on a single atom or a pair of atoms. (Section 9.6)
In NMR spectroscopy, a signal that is comprised of two peaks.
A process in a chemical reaction that occurs in a single step. An overall chemical reaction consists of one or more elementary reactions or steps. (Section 14.6)
A reaction that produces one enantiomer in preference to the other.
A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.
A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.
The relationship among the pH, pKa, and the concentrations of acid and conjugate base in an aqueous solution: pH = pKa + log 3base4 3acid4. (Section 17.2)
Heterolytic bond cleavage
Cleavage of a bond so that one fragment retains both electrons and the other retains none.
Solids that are composed of ions. (Section 12.1)
An electron-pair donor. (Section 16.11)
Common name for silicon dioxide. (Section 22.4)
A reaction that obeys conservation of orbital symmetry.
A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond