- 22.2SE.1PE: Predicting the Products of Chemical ReactionsPredict the products f...
- 22.2SE.2PE: Predicting the Products of Chemical ReactionsPredict the products f...
Solutions for Chapter 22.2SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.
A !CH2CH"CH2 group.
The wave function (?) of an electron in an atom. (7.5)
The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.
The pressure at which a gas at its critical temperature is converted to a liquid state. (Section 11.4)
The ratio of an object’s mass to its volume. (Section 1.4)
A term associatedwith the probability of finding an electron in aparticular region of space.
Any process with a positive DH (the system receives energy from the surroundings).
A barbed curved arrow used to show the change in position of a single electron.
gas constant (R)
The constant of proportionality in the ideal-gas equation. (Section 10.4)
An amine in which nitrogen is one of the atoms of a ring
A measure of the amount of material in an object. It measures the resistance of an object to being moved. In SI units, mass is measured in kilograms. (Section 1.4)
nematic liquid crystalline phase
A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)
oxidation number (oxidation state)
A positive or negative whole number assigned to an element in a molecule or ion on the basis of a set of formal rules; to some degree it reflects the positive or negative character of that atom. (Section 4.4)
Pauli exclusion principle
The rule that states that an atomic orbital or molecular orbital can accommodate a maximum of two electrons with opposite spin.
The conjugate base of phenol or a substituted phenol.
The stabilization associated with the delocalization of electrons via resonance.
Exchange of the !OR or !OAr group of an ester for another !OR or !OAr group.
Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.