- 14.3SE.1PE: Relating Rates at Which Products Appear and Reactants Disappear(a) ...
- 14.3SE.2PE: Relating Rates at Which Products Appearand Reactants Disappear(a) H...
Solutions for Chapter 14.3SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
An aldol addition followed by dehydration to give an a,bunsaturated ketone or aldehyde.
The product obtained when the aldehyde group of an aldose is oxidized.
Members of group 1A in the periodic table. (Section 7.7)
base-dissociation constant (Kb)
An equilibrium constant that expresses the extent to which a base reacts with solvent water, accepting a proton and forming OH-1aq2. (Section 16.7)
A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.
Energy stored within the structural units of chemical substances. (6.1)
An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)
Compound containing only carbon, chlorine, and fluorine.
A compound in which two p bonds are separated from each other by exactly one s bond.
An alkane whose structure contains a ring.
A molecule containing an !S!S! group
Fourier transform NMR (FT-NMR)
The modern NMR method that is based on a constant magnetic fi eld, a short pulse of electromagnetic radiation, and a mathematical Fourier transform to produce the spectrum
A law stating that the rate of effusion of a gas is inversely proportional to the square root of its molecular weight. (Section 10.8)
The highest occupied molecular orbital.
The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).
The row of elements that lie in a horizontal row in the periodic table. (Section 2.5)
A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).
A radioactive nuclide. (Section 21.1)
The sloweststep in a multistep reaction which determines the rate of the reaction.
An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter
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