- 16.6SE.1PE: Calculating pH from [H+]Calculate the pH values for the two solutio...
- 16.6SE.2PE: Calculating pH from [H+]Calculate the pH values for the two solutio...
Solutions for Chapter 16.6SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A compound that possesses a hydroxyl group (OH).
The amount of acid or base a buffer can neutralize before the pH begins to change appreciably. (Section 17.2)
Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)
complete ionic equation
A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)
A reaction in which two smaller molecules combine to form a larger molecule. Water is invariably one of the products of such a reaction. (24.4)
A neutral species containing one or more complex ions. (23.3)
A saturated hydrocarbon that contains carbons joined to form a ring
A lithium dialkyl cuprate (R2CuLi).
A term that describes the position of equilibrium for a reaction: Keq = 3H3O+ 4 3A- 4 3HA4 3H2O4
A type of carbocation rearrangement in which a methyl group migrates.
Nucleophilic aromatic substitution
A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.
partially condensed structures
A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.
Polyunsaturated fatty acid
A fatty acid with two or more carbon-carbon double bonds in its hydrocarbon chain
A group that is used during synthesis to protect a functional group from the reaction conditions.
radioactive decay chain
A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one. Also called nuclear disintegration series. (Section 21.2)
In NMR spectroscopy, a signal that is comprised of only one peak.
A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.
An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.
A term used to indicate that exactly three alkyl groups are attached directly to a particular position. For example, a tertiary carbocation has three alkyl groups attached directly to the electrophilic carbon atom (C+).
A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.