- 1. Intro to General Chemistry3h 58m
- Classification of Matter18m
- Physical & Chemical Changes19m
- Chemical Properties7m
- Physical Properties6m
- Intensive vs. Extensive Properties13m
- Temperature12m
- Scientific Notation13m
- SI Units8m
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- Significant Figures9m
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- Significant Figures: In Calculations17m
- Conversion Factors16m
- Dimensional Analysis24m
- Density12m
- Density of Geometric Objects19m
- Density of Non-Geometric Objects5m
- 2. Atoms & Elements4h 34m
- The Atom10m
- Subatomic Particles17m
- Isotopes17m
- Ions27m
- Atomic Mass33m
- Periodic Table: Classifications11m
- Periodic Table: Group Names8m
- Periodic Table: Representative Elements & Transition Metals7m
- Periodic Table: Element Symbols6m
- Periodic Table: Elemental Forms6m
- Periodic Table: Phases9m
- Periodic Table: Charges20m
- Calculating Molar Mass10m
- Mole Concept31m
- Law of Conservation of Mass5m
- Law of Definite Proportions12m
- Atomic Theory9m
- Law of Multiple Proportions8m
- Millikan Oil Drop Experiment8m
- Rutherford Gold Foil Experiment11m
- 3. Chemical Reactions4h 34m
- Empirical Formula18m
- Molecular Formula21m
- Combustion Analysis39m
- Combustion Apparatus16m
- Polyatomic Ions25m
- Naming Ionic Compounds12m
- Writing Ionic Compounds8m
- Naming Ionic Hydrates8m
- Naming Acids23m
- Naming Molecular Compounds8m
- Balancing Chemical Equations14m
- Stoichiometry20m
- Limiting Reagent18m
- Percent Yield21m
- Mass Percent6m
- Functional Groups in Chemistry11m
- 4. BONUS: Lab Techniques and Procedures1h 25m
- 5. BONUS: Mathematical Operations and Functions52m
- 6. Chemical Quantities & Aqueous Reactions4h 17m
- Solutions9m
- Molarity22m
- Osmolarity15m
- Dilutions15m
- Solubility Rules16m
- Electrolytes24m
- Molecular Equations21m
- Gas Evolution Equations13m
- Solution Stoichiometry14m
- Complete Ionic Equations18m
- Calculate Oxidation Numbers16m
- Redox Reactions20m
- Balancing Redox Reactions: Acidic Solutions17m
- Balancing Redox Reactions: Basic Solutions17m
- Activity Series11m
- 7. Gases3h 58m
- Pressure Units6m
- The Ideal Gas Law18m
- The Ideal Gas Law Derivations18m
- The Ideal Gas Law Applications6m
- Chemistry Gas Laws14m
- Chemistry Gas Laws: Combined Gas Law12m
- Mole Fraction of Gases6m
- Partial Pressure19m
- The Ideal Gas Law: Molar Mass13m
- The Ideal Gas Law: Density14m
- Gas Stoichiometry18m
- Standard Temperature and Pressure14m
- Effusion15m
- Root Mean Square Speed9m
- Kinetic Energy of Gases10m
- Maxwell-Boltzmann Distribution8m
- Velocity Distributions4m
- Kinetic Molecular Theory16m
- Van der Waals Equation9m
- 8. Thermochemistry3h 2m
- Nature of Energy6m
- Kinetic & Potential Energy11m
- First Law of Thermodynamics7m
- Internal Energy8m
- Endothermic & Exothermic Reactions10m
- Heat Capacity23m
- Constant-Pressure Calorimetry26m
- Constant-Volume Calorimetry11m
- Thermal Equilibrium8m
- Thermochemical Equations14m
- Formation Equations11m
- Enthalpy of Formation14m
- Hess's Law26m
- 9. Quantum Mechanics3h 4m
- Wavelength and Frequency6m
- Speed of Light9m
- The Energy of Light13m
- Electromagnetic Spectrum10m
- Photoelectric Effect20m
- De Broglie Wavelength9m
- Heisenberg Uncertainty Principle17m
- Bohr Model14m
- Emission Spectrum5m
- Bohr Equation13m
- Introduction to Quantum Mechanics5m
- Quantum Numbers: Principal Quantum Number5m
- Quantum Numbers: Angular Momentum Quantum Number10m
- Quantum Numbers: Magnetic Quantum Number11m
- Quantum Numbers: Spin Quantum Number10m
- Quantum Numbers: Number of Electrons11m
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- 10. Periodic Properties of the Elements3h 45m
- The Electron Configuration27m
- The Electron Configuration: Condensed4m
- The Electron Configurations: Exceptions13m
- The Electron Configuration: Ions12m
- Paramagnetism and Diamagnetism13m
- The Electron Configuration: Quantum Numbers17m
- Valence Electrons of Elements12m
- Periodic Trend: Metallic Character6m
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- Periodic Trend: Ionic Radius14m
- Periodic Trend: Ionization Energy17m
- Periodic Trend: Successive Ionization Energies15m
- Periodic Trend: Electron Affinity10m
- Periodic Trend: Electronegativity7m
- Periodic Trend: Effective Nuclear Charge26m
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- 11. Bonding & Molecular Structure3h 51m
- Lewis Dot Symbols10m
- Chemical Bonds13m
- Dipole Moment15m
- Octet Rule10m
- Formal Charge12m
- Lewis Dot Structures: Neutral Compounds20m
- Lewis Dot Structures: Sigma & Pi Bonds15m
- Lewis Dot Structures: Ions15m
- Lewis Dot Structures: Exceptions14m
- Lewis Dot Structures: Acids17m
- Resonance Structures25m
- Average Bond Order4m
- Bond Energy17m
- Coulomb's Law7m
- Lattice Energy16m
- Born Haber Cycle15m
- 12. Molecular Shapes & Valence Bond Theory2h 11m
- 13. Liquids, Solids & Intermolecular Forces2h 41m
- Molecular Polarity10m
- Intermolecular Forces22m
- Intermolecular Forces and Physical Properties12m
- Clausius-Clapeyron Equation22m
- Phase Diagrams13m
- Heating and Cooling Curves28m
- Atomic, Ionic, and Molecular Solids11m
- Crystalline Solids6m
- Simple Cubic Unit Cell7m
- Body Centered Cubic Unit Cell14m
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- 14. Solutions3h 17m
- Solutions: Solubility and Intermolecular Forces20m
- Molality18m
- Parts per Million (ppm)13m
- Mole Fraction of Solutions9m
- Solutions: Mass Percent12m
- Types of Aqueous Solutions8m
- Intro to Henry's Law4m
- Henry's Law Calculations12m
- The Colligative Properties17m
- Boiling Point Elevation18m
- Freezing Point Depression10m
- Osmosis21m
- Osmotic Pressure10m
- Vapor Pressure Lowering (Raoult's Law)19m
- 15. Chemical Kinetics3h 1m
- 16. Chemical Equilibrium2h 31m
- 17. Acid and Base Equilibrium5h 5m
- Acids Introduction9m
- Bases Introduction7m
- Binary Acids15m
- Oxyacids10m
- Bases14m
- Amphoteric Species5m
- Arrhenius Acids and Bases5m
- Bronsted-Lowry Acids and Bases21m
- Lewis Acids and Bases13m
- The pH Scale17m
- Auto-Ionization9m
- Ka and Kb16m
- pH of Strong Acids and Bases9m
- Ionic Salts17m
- pH of Weak Acids31m
- pH of Weak Bases32m
- Diprotic Acids and Bases8m
- Diprotic Acids and Bases Calculations30m
- Triprotic Acids and Bases10m
- Triprotic Acids and Bases Calculations17m
- 18. Aqueous Equilibrium4h 47m
- Intro to Buffers21m
- Henderson-Hasselbalch Equation19m
- Intro to Acid-Base Titration Curves13m
- Strong Titrate-Strong Titrant Curves9m
- Weak Titrate-Strong Titrant Curves15m
- Acid-Base Indicators8m
- Titrations: Weak Acid-Strong Base38m
- Titrations: Weak Base-Strong Acid41m
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- Titrations: Diprotic & Polyprotic Buffers32m
- Solubility Product Constant: Ksp17m
- Ksp: Common Ion Effect18m
- Precipitation: Ksp vs Q12m
- Selective Precipitation9m
- Complex Ions: Formation Constant18m
- 19. Chemical Thermodynamics1h 51m
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- 21. Nuclear Chemistry2h 37m
- Intro to Radioactivity10m
- Alpha Decay9m
- Beta Decay7m
- Gamma Emission7m
- Electron Capture & Positron Emission9m
- Neutron to Proton Ratio7m
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- Band of Stability: Electron Capture & Positron Emission4m
- Band of Stability: Overview14m
- Measuring Radioactivity7m
- Rate of Radioactive Decay12m
- Radioactive Half-Life16m
- Mass Defect19m
- Nuclear Binding Energy14m
- 22. Organic Chemistry5h 4m
- Introduction to Organic Chemistry8m
- Structural Formula8m
- Condensed Formula10m
- Skeletal Formula6m
- Spatial Orientation of Bonds3m
- Intro to Hydrocarbons16m
- Isomers11m
- Chirality12m
- Functional Groups in Chemistry11m
- Naming Alkanes4m
- The Alkyl Groups9m
- Naming Alkanes with Substituents13m
- Naming Cyclic Alkanes6m
- Naming Other Substituents8m
- Naming Alcohols11m
- Naming Alkenes11m
- Naming Alkynes9m
- Naming Ketones5m
- Naming Aldehydes5m
- Naming Carboxylic Acids4m
- Naming Esters8m
- Naming Ethers5m
- Naming Amines5m
- Naming Benzene7m
- Alkane Reactions7m
- Intro to Addition Reactions4m
- Halogenation Reactions4m
- Hydrogenation Reactions3m
- Hydrohalogenation Reactions7m
- Alcohol Reactions: Substitution Reactions4m
- Alcohol Reactions: Dehydration Reactions9m
- Intro to Redox Reactions8m
- Alcohol Reactions: Oxidation Reactions7m
- Aldehydes and Ketones Reactions6m
- Ester Reactions: Esterification4m
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- Carboxylic Acid Reactions4m
- Amine Reactions3m
- Amide Formation4m
- Benzene Reactions10m
- 23. Chemistry of the Nonmetals2h 39m
- Main Group Elements: Bonding Types4m
- Main Group Elements: Boiling & Melting Points7m
- Main Group Elements: Density11m
- Main Group Elements: Periodic Trends7m
- The Electron Configuration Review16m
- Periodic Table Charges Review20m
- Hydrogen Isotopes4m
- Hydrogen Compounds11m
- Production of Hydrogen8m
- Group 1A and 2A Reactions7m
- Boron Family Reactions7m
- Boron Family: Borane7m
- Borane Reactions7m
- Nitrogen Family Reactions12m
- Oxides, Peroxides, and Superoxides12m
- Oxide Reactions4m
- Peroxide and Superoxide Reactions6m
- Noble Gas Compounds3m
- 24. Transition Metals and Coordination Compounds3h 19m
- Atomic Radius & Density of Transition Metals11m
- Electron Configurations of Transition Metals7m
- Electron Configurations of Transition Metals: Exceptions11m
- Paramagnetism and Diamagnetism10m
- Ligands10m
- Complex Ions5m
- Coordination Complexes7m
- Classification of Ligands11m
- Coordination Numbers & Geometry9m
- Naming Coordination Compounds22m
- Writing Formulas of Coordination Compounds8m
- Isomerism in Coordination Complexes17m
- Orientations of D Orbitals4m
- Intro to Crystal Field Theory10m
- Crystal Field Theory: Octahedral Complexes5m
- Crystal Field Theory: Tetrahedral Complexes4m
- Crystal Field Theory: Square Planar Complexes4m
- Crystal Field Theory Summary8m
- Magnetic Properties of Complex Ions9m
- Strong-Field vs Weak-Field Ligands6m
- Magnetic Properties of Complex Ions: Octahedral Complexes11m
Calculate Oxidation Numbers: Videos & Practice Problems
To Calculate Oxidation Numbers, use standard oxidation number rules and remember that oxidation numbers do not always match real charges. Elements in their standard or natural state have an oxidation state of 0, while a monoatomic ion has an oxidation number equal to its charge. Key patterns include Group 1A as +1, Group 2A as +2, fluorine as −1, and chlorine, bromine, and iodine usually as −1 unless bonded to oxygen.
Hydrogen is +1 with nonmetals and −1 with metals or boron. Oxygen is usually −2, but it changes in a peroxide to −1 and in a superoxide to \(-\frac{1}{2}\) . For elements not covered directly by the rules, assign the unknown element as \(x\) , apply known values to the other atoms, include subscripts, and set the sum of all oxidation numbers equal to the overall charge of the compound or ion.
Calculating Oxidation Numbers is the first pivotal step in understanding redox reactions.
Calculate Oxidation Numbers
Elements in Natural State have an oxidation number of zero:H2, N2, O2, F2, P4, S8, Cl2, Se8, Br2.
Oxidation Numbers Example
Oxidation Numbers Example Video Summary

Oxidation Numbers in Ions
Oxidation Numbers in Ions Video Summary
When an element gains a charge, it transitions from its standard state, resulting in an oxidation number that is no longer zero. An ion, defined as an element or compound with a positive or negative charge, can be categorized into two types: cations, which are positively charged ions, and anions, which are negatively charged ions. For monoatomic ions, the oxidation number directly corresponds to its charge. For instance, the aluminum ion, which belongs to group 3A, has a charge of +3. Therefore, in its ionic form, the oxidation number of aluminum is also +3.
It is crucial to note that this relationship between charge and oxidation number holds true only when the element is in its ion form. In other scenarios, the oxidation number may vary significantly depending on the element's chemical environment. However, for the current context, if you encounter an ion and its charge, you can confidently equate that charge to its oxidation number. This foundational understanding will be essential as you progress to more complex examples and applications in chemistry.
Oxidation number of monoatomic ions equals to their charge.
Oxidation Numbers in Ions Example
Oxidation Numbers in Ions Example Video Summary
Understanding oxidation numbers is crucial in chemistry, particularly when analyzing the ionic forms of elements. Each element has a characteristic oxidation state that can be determined based on its position in the periodic table. For instance, silver, a transition metal, consistently exhibits an oxidation number of +1. This is an exception among transition metals, which typically have multiple oxidation states.
Scandium, also a transition metal located in group 3B, generally has an oxidation state of +3. Sodium, found in group 1A, has a stable oxidation number of +1. In contrast, sulfur, which is in group 6A, typically has an oxidation state of -2.
When tasked with identifying the element with the most positive oxidation number, it is essential to compare these values. In this case, scandium with its +3 oxidation state stands out as the highest positive charge among the options provided. Therefore, the correct answer is that scandium has the most positive oxidation number, which is +3. This foundational knowledge of oxidation states is vital as it lays the groundwork for more advanced topics in chemistry, including redox reactions and coordination chemistry.
Which of the following elements would have the lowest oxidation number?
Oxidation Number Rules
Oxidation Number Rules Video Summary
Understanding oxidation numbers is crucial in chemistry, as they help us determine the distribution of electrons in compounds. Oxidation numbers do not always reflect actual charges, so specific rules are necessary for accurate calculations. Here are the key rules for determining oxidation numbers based on the elements involved:
For elements in Group 1A, the oxidation number is always +1 when they are part of a compound. Similarly, Group 2A elements have an oxidation number of +2. Fluorine consistently has an oxidation number of -1 in all compounds.
Hydrogen presents a unique case; it can have an oxidation number of +1 or -1 depending on the element it is bonded to. When hydrogen is connected to nonmetals (like chlorine, oxygen, or nitrogen), its oxidation number is +1. Conversely, when bonded to metals or boron, such as in sodium hydride (NaH) or calcium hydride (CaH2), hydrogen's oxidation number is -1.
Oxygen's oxidation number is typically -2, except in specific cases. In peroxides, where two Group 1A elements are bonded to two oxygen atoms (e.g., hydrogen peroxide, H2O2), the oxidation number of oxygen is -1. In superoxides, which consist of one Group 1A element and two oxygen atoms (e.g., potassium superoxide, KO2), the oxidation number of oxygen is -1/2. If neither of these conditions is met, oxygen retains its -2 oxidation state.
For Group 7A elements, such as chlorine, bromine, and iodine, the oxidation number is generally -1, except when they are bonded to oxygen. In such cases, the oxidation number must be calculated based on the specific compound.
By applying these rules, one can systematically determine the oxidation number of any element within a compound, facilitating a deeper understanding of chemical reactions and bonding.
Specific rules exist for calculating oxidation numbers of group 1A and 2A elements, F, H, O and Halogens.
Oxidation Number Rules Example
Oxidation Number Rules Example Video Summary
To determine which compound has oxygen with the lowest oxidation state, we can analyze several examples based on their chemical formulas and the oxidation states of oxygen in each case.
Starting with sodium oxide, NaO2, we note that it contains one Group 1A element (sodium) and two oxygen atoms. This configuration indicates that it is a superoxide, where the oxidation state of oxygen is -½.
Next, we examine carbon dioxide, CO2. Since carbon is in Group 4A, it does not meet the criteria for being a superoxide or a peroxide. A peroxide requires two Group 1A elements with two oxygens, which is not the case here. Therefore, the oxidation state of oxygen in CO2 is -2.
Moving on to cesium peroxide, Cs2O2, we see that it contains two cesium atoms (Group 1A) and two oxygen atoms. This fits the definition of a peroxide, resulting in an oxidation state of -1 for oxygen.
Finally, we consider diatomic oxygen, O2, which is in its standard state. The oxidation state of oxygen in this form is 0.
Comparing the oxidation states from all examples, we find that carbon dioxide (CO2) has the lowest oxidation state for oxygen at -2. Thus, it is the compound with the most negative oxidation state for oxygen among the options provided.
Determining Oxidation Numbers
Determining Oxidation Numbers Video Summary
Calculate Oxidation Numbers Example
Calculate Oxidation Numbers Example Video Summary
To determine the oxidation number of the carbon atom in the acetate ion (C2H3O2-), we start by assigning oxidation states based on common rules. In this case, we denote the oxidation number of carbon as x. The oxidation state of hydrogen, when bonded to nonmetals, is typically +1, while oxygen generally has an oxidation state of -2 unless it is part of a peroxide or superoxide.
In the acetate ion, we have two carbon atoms, three hydrogen atoms, and two oxygen atoms. The equation representing the total oxidation states can be set up as follows:
2x + 3(+1) + 2(-2) = -1
Breaking this down, we have:
2x + 3 - 4 = -1
This simplifies to:
2x - 1 = -1
Next, we add 1 to both sides:
2x = 0
Dividing both sides by 2 gives us:
x = 0
Thus, the oxidation number of carbon in the acetate ion is 0. This illustrates that an element can have an oxidation state of 0 even when it is not in its elemental form, as seen in this example.
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To calculate oxidation numbers in compounds, start with standard rules: Group 1A elements have an oxidation number of +1, Group 2A elements are +2, fluorine is always -1, and chlorine, bromine, and iodine are usually -1 unless bonded to oxygen. Hydrogen is +1 when bonded to nonmetals and -1 when bonded to metals or boron. Oxygen is typically -2, except in peroxides where it is -1, and in superoxides where it is -½. For elements not listed, assign them as , use known oxidation numbers for other atoms, multiply by their subscripts, and set the sum equal to the overall charge of the compound or ion. This systematic approach helps determine unknown oxidation states accurately.
In its natural or elemental state, an element's oxidation number is always zero. This includes monoatomic elements like noble gases and diatomic molecules such as H2, N2, O2, F2, Cl2, Br2, and I2. Some elements exist as polyatomic molecules in nature, like P4 and S8. Since these atoms are not combined with different elements, they have no net gain or loss of electrons, so their oxidation state is . This is a fundamental starting point when calculating oxidation numbers in compounds.
For monoatomic ions, the oxidation number is equal to the ion's charge. For example, an aluminum ion (Al3+) has an oxidation number of +3. This is because the ion has lost three electrons, giving it a +3 charge. However, this direct equivalence applies only to ions, not atoms in compounds where oxidation numbers can vary depending on bonding. Recognizing this helps in quickly assigning oxidation states to ions in redox reactions and other chemical processes.
To find the oxidation number of an unknown element in a compound, follow these four steps: (1) Assign the unknown element as . (2) Use known oxidation numbers for other elements in the compound based on standard rules (e.g., oxygen is usually -2 unless in peroxides or superoxides). (3) Multiply the oxidation numbers by their respective subscripts in the chemical formula. (4) Set up an equation where the sum of all oxidation numbers equals the overall charge of the compound or ion, then solve for . This method ensures a systematic and accurate determination of unknown oxidation states.
Oxygen's oxidation number varies depending on the compound. Typically, oxygen has an oxidation number of -2. However, in peroxides (compounds containing an O–O bond, such as H2O2), oxygen has an oxidation number of -1. In superoxides, where one Group 1A element bonds with two oxygens (e.g., KO2), oxygen's oxidation number is -½. Recognizing these exceptions is crucial when calculating oxidation numbers in compounds containing oxygen.