- 4.12SE.1PE: Calculating Molar Concentrations of IonsWhat is the molar concentra...
- 4.12SE.2PE: Calculating Molar Concentrations of IonsWhat is the molar concentra...
Solutions for Chapter 4.12SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
The product obtained from 1,4-addition across a conjugated p system.
A compound that contains at least one amino group and at least one carboxyl group. (25.3)
A cyclic hydrocarbon with a continuous alternation of single and double bonds.
In a bicyclic system, the carbon atoms where the rings are fused together.
A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)
A substance composed of atoms of two or more elements chemically united in fixed proportions. (1.4)
A chemical bond formed between two atoms by sharing one or more pairs of electrons.
A unit of measure fordipole moments, where 1 debye = 10-18 esu×cm.
Stereoisomers that are not mirror images of one another.
electromagnetic radiation (radiant energy)
A form of energy that has wave characteristics and that propagates through a vacuum at the characteristic speed of 3.00 * 108 m >s. (Section 6.1)
enthalpy of reaction
The enthalpy change associated with a chemical reaction. (Section 5.4)
A cyclic amide.
A cyclic ester.
A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.
net ionic equation
A chemical equation for a solution reaction in which soluble strong electrolytes are written as ions and spectator ions are omitted. (Section 4.2)
An organic compound containing at least one halogen.
Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.
Refers to two hydrogens bonded to a carbon atom. When a different atom replaces one or the other, the carbon becomes a chiral center. The hydrogens of the CH2 group of ethanol, for example, are prochiral. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol
An intermediate that has both a negative charge and an unpaired electron.
A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene
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