- 18.104.22.168.15: Which electrons do a Lewis structure show?
- 22.214.171.124.16: In a polyatomic ion, where is the charge located?
- 126.96.36.199.17: How many electrons are shared by two atoms that form a triple bond?
- 188.8.131.52.18: What do resonance structures represent?
- 184.108.40.206.19: How do the names for SO2 and SO3 differ?
- 220.127.116.11.20: Draw a Lewis structure for an atom that has the electron configurat...
- 18.104.22.168.21: Draw Lewis structures for each compound: a. BrF c. Cl2O b. N(CH3)3 ...
- 22.214.171.124.22: Draw three resonance structures for SO3.
- 126.96.36.199.23: Name the following compounds. a. SnI4 c. PCl3 b. N2O3 d. CSe2
- 188.8.131.52.24: Write the formula for each compound: a. phosphorus pentabromide b. ...
- 184.108.40.206.25: Compare and contrast the Lewis structures for krypton and radon.
- 220.127.116.11.26: Do you always follow the octet rule when drawing a Lewis structure?...
- 18.104.22.168.27: What is incorrect about the name monosulfur dioxide for the compoun...
Solutions for Chapter 6.2: Drawing and Naming Molecules
Full solutions for Modern Chemistry: Student Edition 2006 | 1st Edition
A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.
A solid whose molecular arrangement lacks the regularly repeating long- range pattern of a crystal. (Section 12.2)
The addition of atoms or groups of atoms to opposite faces of a carbon-carbon double bond.
The electronic structure of a solid, defining the allowed ranges of energy for electrons in a solid. (Section 12.7)
A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.
The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)
A nuclear reactor that produces more fissionable materials than it uses. (19.5)
A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center
When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.
Dalton’s law of partial pressures.
The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)
law of constant composition
A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)
Anything that occupies space and has mass; the physical material of the universe. (Section 1.1)
A method for building a peptide from protected building blocks.
The extent to which an element exhibits the physical and chemical properties characteristic of metals, for example, luster, malleability, ductility, and good thermal and electrical conductivity. (Section 7.6)
A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.
On an aromatic ring, the C2 position.
A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.
An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter
A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.
Groups that weakly deactivate an aromatic ring toward electrophilic aromatic substitution, thereby decreasing the rate of the reaction.