目录

  • 1 Nomenclature
    • 1.1 Nomenclature
    • 1.2 Inorganic compounds
    • 1.3 Organic compounds
  • 2 Atom
    • 2.1 Basic Atomic Theory
    • 2.2 Evolution of Atomic Theory
    • 2.3 Atomic Structure and Symbolism
    • 2.4 Isotopes
    • 2.5 Early development of the periodic table of elements
    • 2.6 Organization of the elements
  • 3 Atoms: the quantum world
    • 3.1 Wave Nature of Light
    • 3.2 Quantized Energy and Photons
    • 3.3 the Bohr Model
    • 3.4 Wave Character of Matter
    • 3.5 Atomic Orbitals
    • 3.6 3D Representation of Orbitals
    • 3.7 Electron Spin
    • 3.8 Electron Configurations
  • 4 Molecular Shape and Structure
    • 4.1 VSEPR theory
    • 4.2 Hybridization
    • 4.3 sp3 hybridization
    • 4.4 sp2 hybridization
    • 4.5 sp hybridization
    • 4.6 Other hybridization
    • 4.7 Multiple Bonds
    • 4.8 Molecular Orbitals
    • 4.9 Second-Row Diatomic Molecules
  • 5 Fundamentals of Thermochemistry
    • 5.1 Systems, States and Processes
    • 5.2 Heat as a Mechanism to Transfer Energy
    • 5.3 Work as a Mechanism to Transfer Energy
    • 5.4 Heat Capacity and Calorimetry
    • 5.5 The First Law of Thermodynamics
    • 5.6 Heats of Reactions - ΔU and ΔH
    • 5.7 Indirect Determination of ΔH - Hess's Law
    • 5.8 Standard Enthalpies of Formation
  • 6 Principles of Thermodynamics
    • 6.1 The Nature of Spontaneous Processes
    • 6.2 Entropy and Spontaneity - A Molecular Statistical Interpretation
    • 6.3 Entropy Changes and Spontaneity
    • 6.4 Entropy Changes in Reversible Processes
    • 6.5 Quantum States, Microstates, and Energy Spreading
    • 6.6 The Third Law of Thermodynamics
    • 6.7 Gibbs Energy
  • 7 Chemical equilibrium
    • 7.1 Equilibrium
    • 7.2 Reversible and irreversible reaction
    • 7.3 Chemical equilirbium
    • 7.4 Chemical equilibrium constant, Kc
    • 7.5 Le Chatelier's principle
    • 7.6 RICE table
    • 7.7 Haber process
  • 8 Acid–Base Equilibria
    • 8.1 Classifications of Acids and Bases
    • 8.2 The Brønsted-Lowry Scheme
    • 8.3 Acid and Base Strength
    • 8.4 Buffer Solutions
    • 8.5 Acid-Base Titration Curves
    • 8.6 Polyprotic Acids
    • 8.7 Exact Treatment of Acid-Base Equilibria
    • 8.8 Organic Acids and Bases
  • 9 Kinetics
    • 9.1 Prelude to Kinetics
    • 9.2 Chemical Reaction Rates
    • 9.3 Factors Affecting Reaction Rates
    • 9.4 Rate Laws
    • 9.5 Integrated Rate Laws
    • 9.6 Collision Theory
    • 9.7 Reaction Mechanisms
    • 9.8 Catalysis
Inorganic compounds

Generally, there are two types of inorganic compounds that can be formed: ionic compounds and molecular compounds. Nomenclature is the process of naming chemical compounds with different names so that they can be easily identified as separate chemicals. Inorganic compounds are compounds that do not deal with the formation of carbohydrates, or simply all other compounds that do not fit into the description of an organic compound. For example, organic compounds include molecules with carbon rings and/or chains with hydrogen atoms (see picture below). Inorganic compounds, the topic of this section, are every other molecule that does not include these distinctive carbon and hydrogen structures.

Compounds between Metals and Nonmetals (Cation and Anion)

Compounds made of a metal and nonmetal are commonly known as Ionic Compounds, where the compound name has an ending of –ideCations have positive charges while anions have negative charges. The net charge of any ionic compound must be zero which also means it must be electrically neutral. For example, one Na+ is paired with one Cl-; one Ca2+ is paired with two Br-. There are two rules that must be followed through:

  • The cation (metal) is always named first with its name unchanged

  • The anion (nonmetal) is written after the cation, modified to end in –ide

Table 1: Cations and Anions:
+1 Charge+2 Charge-1 Charge-2 Charge-3 Charge-4 Charge
Group 1A elementsGroup 2A elementsGroup 7A elementsGroup 6A elementsGroup 5A elementsGroup 4A elements
Hydrogen: H+Beryllium: Be2+Hydride: H-Oxide: O2-Nitride: N3-Carbide: C4-
Lithium: Li+Magnesium: Mg2+Fluoride: F-Sulfide: S2-Phosphide: P3-
Soduim: Na+Calcium: Ca2+Chloride: Cl-


Potassium: K+Strontium: Sr2+Bromide: Br-


Rubidium: Rb+Barium: Ba2+Iodide: I-


Cesium: Cs+




EXAMPLE 1

Na+ ClNaCl Ca2+ + 2Br- CaBr2

Sodium + Chlorine = Sodium Chloride;  Calcium + Bromine = Calcium Bromide

The transition metals may form more than one ion, thus it is needed to be specified which particular ion we are talking about. This is indicated by assigning a Roman numeral after the metal. The Roman numeral denotes the charge and the oxidation state of the transition metal ion. For example, iron can form two common ions, Fe2+ and Fe3+. To distinguish the difference, Fe2+ would be named iron (II) and Fe3+ would be named iron (III).

Table of Transition Metal and Metal Cations:
+1 Charge+2 Charge+3 Charge+4 Charge
Copper(I): Cu+Copper(II): Cu2+Aluminum: Al3+Lead(IV): Pb4+
Silver: Ag+Iron(II): Fe2+Iron(III): Fe3+Tin(IV): Sn4+

Cobalt(II): Co2+Cobalt(III): Co3+

Tin(II): Sn2+


Lead(II): Pb2+


Nickel: Ni2+


Zinc: Zn2+

EXAMPLE 2

Ions:Fe2+2Cl-Fe3++ 3Cl-
Compound:FeCl2FeCl3
NomenclatureIron (II) ChlorideIron (III) Chloride

However, some of the transition metals' charges have specific Latin names. Just like the other nomenclature rules, the ion of the transition metal that has the lower charge has the Latin name ending with -ous and the one with the the higher charge has a Latin name ending with -ic. The most common ones are shown in the table below:

Transition Metal Ion with Roman NumeralLatin name
Copper (I): Cu+Cuprous
Copper (II): Cu2+Cupric
Iron (II): Fe2+Ferrous
Iron (III): Fe3+Ferric
Lead (II): Pb2+Plumbous
Lead (IV): Pb4+Plumbic
Mercury (I): Hg22+Mercurous
Mercury (II): Hg2+Mercuric
Tin (II): Sn2+Stannous
Tin (IV): Sn4+Stannic

Several exceptions apply to the Roman numeral assignment: Aluminum, Zinc, and Silver. Although they belong to the transition metal category, these metals do not have Roman numerals written after their names because these metals only exist in one ion. Instead of using Roman numerals, the different ions can also be presented in plain words. The metal is changed to end in –ous or –ic.

  • -ous ending is used for the lower oxidation state

  • -ic ending is used for the higher oxidation state

EXAMPLE 3

CompoundCu2OCuOFeCl2FeCl3
ChargeCharge of copper is +1Charge of copper is +2Charge of iron is +2Charge of iron is +3
NomenclatureCuprous OxideCupric OxideFerrous ChlorideFerric Chloride

However, this -ous/-ic system is inadequate in some cases, so the Roman numeral system is preferred. This system is used commonly in naming acids, where H2SO4 is commonly known as Sulfuric Acid, and H2SO3 is known as Sulfurous Acid.

Compounds between Nonmetals and Nonmetals

Compounds that consist of a nonmetal bonded to a nonmetal are commonly known as Molecular Compounds, where the element with the positive oxidation state is written first. In many cases, nonmetals form more than one binary compound, so prefixes are used to distinguish them.

# of Atoms12345678910
PrefixesMono-Di-Tri-Tetra-Penta-Hexa-Hepta-Octa-Nona-Deca-

EXAMPLE 4

CO = carbon monoxide BCl3 = borontrichloride

CO2 = carbon dioxide N2O5 =dinitrogen pentoxide

The prefix mono- is not used for the first element. If there is not a prefix before the first element, it is assumed that there is only one atom of that element.

Binary Acids

Although HF can be named hydrogen fluoride, it is given a different name for emphasis that it is an acid. An acid is a substance that dissociates into hydrogen ions (H+) and anions in water. A quick way to identify acids is to see if there is an H (denoting hydrogen) in front of the molecular formula of the compound. To name acids, the prefix hydro- is placed in front of the nonmetal modified to end with –ic. The state of acids is aqueous (aq) because acids are found in water.

Some common binary acids include:

HF (g) = hydrogen fluoride -> HF (aq) = hydrofluoric acid

HBr (g) = hydrogen bromide -> HBr (aq) = hydrobromic acid

HCl (g) = hydrogen chloride -> HCl (aq) = hydrochloric acid

H2S (g) = hydrogen sulfide -> H2S (aq) = hydrosulfuricacid

It is important to include (aq) after the acids because the same compounds can be written in gas phase with hydrogen named first followed by the anion ending with –ide.

EXAMPLE 5

hypo____ite ____ite ____ate per____ate

ClO- ClO2- ClO3- ClO4-

hypochlorite chlorite chlorate perchlorate

---------------->

As indicated by the arrow, moving to the right, the following trends occur:

Increasing number of oxygen atoms

Increasing oxidation state of the nonmetal

(Usage of this example can be seen from the set of compounds containing Cl and O)

This occurs because the number of oxygen atoms are increasing from hypochlorite to perchlorate, yet the overall charge of the polyatomic ion is still -1. To correctly specify how many oxygen atoms are in the ion, prefixes and suffixes are again used.

Polyatomic Ions

In polyatomic ions, polyatomic (meaning two or more atoms) are joined together by covalent bonds. Although there may be a element with positive charge like H+, it is not joined with another element with an ionic bond. This occurs because if the atoms formed an ionic bond, then it would have already become a compound, thus not needing to gain or loose any electrons. Polyatomic anions are more common than polyatomic cations as shown in the chart below. Polyatomic anions have negative charges while polyatomic cations have positive charges. To indicate different polyatomic ions made up of the same elements, the name of the ion is modified according to the example below:

Table: Common Polyatomic ions
Name: Cation/AnionFormula
Ammonium ionNH4+
Hydronium ion

H3O+

Acetate ion

C2H3O2-

Arsenate ion

AsO43-

Carbonate ion

CO32-

Hypochlorite ion

ClO-

Chlorite ion

ClO2-

Chlorate ion

ClO3-

Perchlorate ion

ClO4-

Chromate ion

CrO42-

Dichromate ion

Cr2O72-

Cyanide ion

CN-

Hydroxide ion

OH-

Nitrite ion

NO2-

Nitrate ion

NO3-

Oxalate ion

C2O42-

Permanganate ion

MnO4-

Phosphate ion

PO43-

Sulfite ion

SO32-

Sulfate ion

SO42-

Thiocyanate ion

SCN-
Thiosulfate ion

S2O32-

To combine the topic of acids and polyatomic ions, there is nomenclature of aqueous acids. Such acids include sulfuric acid (H2SO4) or carbonic acid (H2CO3). To name them, follow these quick, simple rules:

  1. If the ion ends in -ate and is added with an acid, the acid name will have an -ic ending. Examples: nitrate ion (NO3-) + H(denoting formation of acid) = nitric acid (HNO3)

  2. If the ion ends in -ite and is added with an acid, then the acid name will have an -ous ending. Example: nitite ion (NO2-) + H+ (denoting formation of acid) = nitrous acid (HNO2)