- 14.2SE.1PE: Calculating an Instantaneous Rate of ReactionUsing Figure, calculat...
- 14.2SE.2PE: Calculating an Instantaneous Rate of ReactionUsing Figure, calculat...
Solutions for Chapter 14.2SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
An amine in which nitrogen is bonded only to alkyl groups.
A form of magnetism in which unpaired electron spins on adjacent sites point in opposite directions and cancel each other’s effects. (Section 23.1)
Benzyl group (C6H5CH2!)
The group derived from toluene by removing a hydrogen from its methyl group.
An electrode at which reduction occurs. (Section 20.3)
A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.
An object that is not superimposable on its mirror image.
A ratio relating the same quantity in two systems of units that is used to convert the units of measurement. (Section 1.6)
The deterioration of metals by an electrochemical process. (18.7)
In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.
An effect that explains why alkyl groups stabilize a carbocation.
law of definite proportions
A law that states that the elemental composition of a pure substance is always the same, regardless of its source; also called the law of constant composition. (Section 1.2)
The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)
The electrophile in a Michael reaction.
From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.
The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)
A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)
The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)
retention of configuration
During a reaction, when the configuration of a chirality center remains unchanged.
Reactions in which one group is replaced by another group.
In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.
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