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Introductory Chemistry - 1st Canadian Edition: Periodic Trends

Introductory Chemistry - 1st Canadian Edition
Periodic Trends
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table of contents
  1. Cover
  2. Title Page
  3. Copyright
  4. Table Of Contents
  5. Acknowledgments
  6. Dedication
  7. About BCcampus Open Education
  8. Chapter 1. What is Chemistry
    1. Some Basic Definitions
    2. Chemistry as a Science
  9. Chapter 2. Measurements
    1. Expressing Numbers
    2. Significant Figures
    3. Converting Units
    4. Other Units: Temperature and Density
    5. Expressing Units
    6. End-of-Chapter Material
  10. Chapter 3. Atoms, Molecules, and Ions
    1. Acids
    2. Ions and Ionic Compounds
    3. Masses of Atoms and Molecules
    4. Molecules and Chemical Nomenclature
    5. Atomic Theory
    6. End-of-Chapter Material
  11. Chapter 4. Chemical Reactions and Equations
    1. The Chemical Equation
    2. Types of Chemical Reactions: Single- and Double-Displacement Reactions
    3. Ionic Equations: A Closer Look
    4. Composition, Decomposition, and Combustion Reactions
    5. Oxidation-Reduction Reactions
    6. Neutralization Reactions
    7. End-of-Chapter Material
  12. Chapter 5. Stoichiometry and the Mole
    1. Stoichiometry
    2. The Mole
    3. Mole-Mass and Mass-Mass Calculations
    4. Limiting Reagents
    5. The Mole in Chemical Reactions
    6. Yields
    7. End-of-Chapter Material
  13. Chapter 6. Gases
    1. Pressure
    2. Gas Laws
    3. Other Gas Laws
    4. The Ideal Gas Law and Some Applications
    5. Gas Mixtures
    6. Kinetic Molecular Theory of Gases
    7. Molecular Effusion and Diffusion
    8. Real Gases
    9. End-of-Chapter Material
  14. Chapter 7. Energy and Chemistry
    1. Formation Reactions
    2. Energy
    3. Stoichiometry Calculations Using Enthalpy
    4. Enthalpy and Chemical Reactions
    5. Work and Heat
    6. Hess’s Law
    7. End-of-Chapter Material
  15. Chapter 8. Electronic Structure
    1. Light
    2. Quantum Numbers for Electrons
    3. Organization of Electrons in Atoms
    4. Electronic Structure and the Periodic Table
    5. Periodic Trends
    6. End-of-Chapter Material
  16. Chapter 9. Chemical Bonds
    1. Lewis Electron Dot Diagrams
    2. Electron Transfer: Ionic Bonds
    3. Covalent Bonds
    4. Other Aspects of Covalent Bonds
    5. Violations of the Octet Rule
    6. Molecular Shapes and Polarity
    7. Valence Bond Theory and Hybrid Orbitals
    8. Molecular Orbitals
    9. End-of-Chapter Material
  17. Chapter 10. Solids and Liquids
    1. Properties of Liquids
    2. Solids
    3. Phase Transitions: Melting, Boiling, and Subliming
    4. Intermolecular Forces
    5. End-of-Chapter Material
  18. Chapter 11. Solutions
    1. Colligative Properties of Solutions
    2. Concentrations as Conversion Factors
    3. Quantitative Units of Concentration
    4. Colligative Properties of Ionic Solutes
    5. Some Definitions
    6. Dilutions and Concentrations
    7. End-of-Chapter Material
  19. Chapter 12. Acids and Bases
    1. Acid-Base Titrations
    2. Strong and Weak Acids and Bases and Their Salts
    3. Brønsted-Lowry Acids and Bases
    4. Arrhenius Acids and Bases
    5. Autoionization of Water
    6. Buffers
    7. The pH Scale
    8. End-of-Chapter Material
  20. Chapter 13. Chemical Equilibrium
    1. Chemical Equilibrium
    2. The Equilibrium Constant
    3. Shifting Equilibria: Le Chatelier’s Principle
    4. Calculating Equilibrium Constant Values
    5. Some Special Types of Equilibria
    6. End-of-Chapter Material
  21. Chapter 14. Oxidation and Reduction
    1. Oxidation-Reduction Reactions
    2. Balancing Redox Reactions
    3. Applications of Redox Reactions: Voltaic Cells
    4. Electrolysis
    5. End-of-Chapter Material
  22. Chapter 15. Nuclear Chemistry
    1. Units of Radioactivity
    2. Uses of Radioactive Isotopes
    3. Half-Life
    4. Radioactivity
    5. Nuclear Energy
    6. End-of-Chapter Material
  23. Chapter 16. Organic Chemistry
    1. Hydrocarbons
    2. Branched Hydrocarbons
    3. Alkyl Halides and Alcohols
    4. Other Oxygen-Containing Functional Groups
    5. Other Functional Groups
    6. Polymers
    7. End-of-Chapter Material
  24. Chapter 17. Kinetics
    1. Factors that Affect the Rate of Reactions
    2. Reaction Rates
    3. Rate Laws
    4. Concentration–Time Relationships: Integrated Rate Laws
    5. Activation Energy and the Arrhenius Equation
    6. Reaction Mechanisms
    7. Catalysis
    8. End-of-Chapter Material
  25. Chapter 18. Chemical Thermodynamics
    1. Spontaneous Change
    2. Entropy and the Second Law of Thermodynamics
    3. Measuring Entropy and Entropy Changes
    4. Gibbs Free Energy
    5. Spontaneity: Free Energy and Temperature
    6. Free Energy under Nonstandard Conditions
    7. End-of-Chapter Material
  26. Appendix A: Periodic Table of the Elements
  27. Appendix B: Selected Acid Dissociation Constants at 25°C
  28. Appendix C: Solubility Constants for Compounds at 25°C
  29. Appendix D: Standard Thermodynamic Quantities for Chemical Substances at 25°C
  30. Appendix E: Standard Reduction Potentials by Value
  31. Glossary
  32. About the Authors
  33. Versioning History

Periodic Trends

Learning Objectives

  1. Be able to state how certain properties of atoms vary based on their relative position on the periodic table.

One of the reasons the periodic table is so useful is because its structure allows us to qualitatively determine how some properties of the elements vary versus their position on the periodic table. The variation of properties versus position on the periodic table is called periodic trends. There is no other tool in science that allows us to judge relative properties of a class of objects like this, which makes the periodic table a very useful tool. Many periodic trends are general. There may be a few points where an opposite trend is seen, but there is an overall trend when considered across a whole row or down a whole column of the periodic table.

Effective Nuclear Charge

Many of the periodic properties of atoms depend on electron configuration; in particular, the valence electrons and their level of attraction to the nucleus.

Valence electrons are simultaneously attracted to the positive charge of the nucleus and screened (repelled) by the negative charges of other electrons. This net nuclear charge felt by valence electrons is known as its effective nuclear charge, Zeff (pronounced “zed-effective”). The effective nuclear charge is always less than the actual nuclear charge, and can be roughly estimated using the following equation:

Z_{\text{eff}}=Z-S

Where Z is the nuclear charge (equal to the number of protons), and S is the screening constant which can be approximated to the number of non-valence or “core” electrons.

For example: try to approximate the effective nuclear charge of magnesium.

First, we must determine the electron configuration of magnesium to determine the number of core electrons:

\ce{Mg}=1s^22s^22p^63s^2=[\ce{Ne}]3s^2

Therefore, magnesium has 10 core electrons from its 1s2, 2s2, and 2p6 orbitals.

Magnesium is element 12, so it has 12 protons and a nuclear charge of 12:

\begin{array}{l} Z_{\text{eff}}=12-10 \\ Z_{\text{eff}}=\phantom{1}2+ \end{array}

Moving left to right across a period on the periodic table, each subsequent element has an additional proton and valence electron, but the core electrons which are responsible for the majority of screening remain the same. This results in a trend that in general the effective nuclear charge increases from left to right across any period of the periodic table.

Moving from top to bottom down a column of the periodic table, we might expect the elements to have a similar effective nuclear charge as they all have the same number of valence electrons. However, we actually see a slight increase in Zeff moving down a column of the periodic table. As the principal quantum number (n) increases, the orbital size increases making the core electron clouds more spread out. These core electron clouds that are more diffuse do not screen as well, giving a slight increase to Zeff (see Figure 8.23 “Increasing Effective Nuclear Charge”).

Effective nuclear charge increases from left to right, top to bottom on the periodic table.
Figure 8.23 “Increasing Effective Nuclear Charge.” The periodic trend for effective nuclear charge.

Atomic Radii

The atomic radius is an indication of the size of an atom. Although the concept of a definite radius of an atom is a bit fuzzy, atoms behave as if they have a certain radius. Such radii can be estimated from various experimental techniques, such as the x-ray crystallography of crystals.

As you go down a column of the periodic table, the atomic radii increase. This is because the valence electron shell is getting a larger and there is a larger principal quantum number, so the valence shell lies physically farther away from the nucleus. This trend can be summarized as follows:

\text{as }\downarrow\text{PT, atomic radius}\uparrow

Where PT stands for “periodic table.” Going across a row on the periodic table, left to right, the trend is different. This is because although the valence shell maintains the same principal quantum number, the number of protons — and hence the nuclear charge — is increasing as you go across the row. The increasing positive charge leads to a larger effective nuclear charge which casts a tighter grip on the valence electrons, so as you go across the periodic table, the atomic radii decrease. Again, we can summarize this trend as follows:

\text{as }\rightarrow\text{PT, atomic radius}\downarrow

Figure 8.24 “Atomic Radii Trends on the Periodic Table” shows spheres representing the atoms of the s and p blocks from the periodic table to scale, showing the two trends for the atomic radius.

Chart of atomic radii trends on the periodic table. Long description available.
Figure 8.24 “Atomic Radii Trends on the Periodic Table.” Although there are some reversals in the trend (e.g., see Po in the bottom row), atoms generally get smaller as you go across the periodic table and larger as you go down any one column. Numbers are the radii in pm. [Long Description]

Example 8.9

Problems

Referring only to a periodic table and not to Figure 8.24 “Atomic Radii Trends on the Periodic Table,” which atom is larger in each pair?

  1. Si or S
  2. S or Te

Solutions

  1. Si is to the left of S on the periodic table, so it is larger because as you go across the row, the atoms get smaller.
  2. S is above Te on the periodic table, so Te is larger because as you go down the column, the atoms get larger.

Test Yourself

Referring only to a periodic table and not to Figure 8.24 “Atomic Radii Trends on the Periodic Table,” which atom is smaller, Ca or Br?

Answer

Br

Ionization Energy

Ionization energy (IE) is the amount of energy required to remove an electron from an atom in the gas phase:

\ce{A(g)}\rightarrow \ce{A^+(g)}+\text{e}^-\hspace{10 mm} \Delta H\equiv \text{IE}

IE is usually expressed in kJ/mol of atoms. It is always positive because the removal of an electron always requires that energy be put in (i.e., it is endothermic). IE also shows periodic trends. As you go down the periodic table, it becomes easier to remove an electron from an atom (i.e., IE decreases) because the valence electron is farther away from the nucleus. Thus:

\text{as }\downarrow\text{PT, IE}\downarrow

However, as you go across the periodic table and the electrons get drawn closer in, it takes more energy to remove an electron; as a result, IE increases:

\text{as }\rightarrow\text{PT, IE}\uparrow

Figure 8.25 “Ionization Energy Trends on the Periodic Table” shows values of IE versus position on the periodic table. Again, the trend isn’t absolute, but the general trends going across and down the periodic table should be obvious.

Ionization energy trends on the periodic table. Long description available.
Figure 8.25 “Ionization Energy on the Periodic Table.” Values are in kJ/mol. [Long Description]

IE also shows an interesting trend within a given atom. This is because more than one IE can be defined by removing successive electrons (if the atom has them to begin with):

\begin{array}{rlrl} \text{IE}_1&\ce{A(g)}&\rightarrow&\ce{A^{\phantom{1}+}(g)}+\text{e}^- \\ \text{IE}_2&\ce{A^+(g)}&\rightarrow&\ce{A^{2+}(g)}+\text{e}^- \\ \text{IE}_3&\ce{A^{2+}(g)}&\rightarrow&\ce{A^{3+}(g)}+\text{e}^- \end{array}

And so forth.

Each successive IE is larger than the previous because an electron is being removed from an atom with a progressively larger positive charge. However, IE takes a large jump when a successive ionization goes down into a new shell. For example, the following are the first three IEs for Mg, whose electron configuration is 1s22s22p63s2:

\begin{array}{llrl} \text{IE}_1=\phantom{1, }738\text{ kJ/mol}&\ce{Mg(g)}&\rightarrow&\ce{Mg^{\phantom{1}+}(g)}+\text{e}^- \\ \text{IE}_2=1,450\text{ kJ/mol}&\ce{Mg^+(g)}&\rightarrow&\ce{Mg^{2+}(g)}+\text{e}^- \\ \text{IE}_3=7,734\text{ kJ/mol}&\ce{Mg^{2+}(g)}&\rightarrow&\ce{Mg^{3+}(g)}+\text{e}^- \end{array}

The second IE is twice the first, which is not a surprise: the first IE involves removing an electron from a neutral atom, while the second one involves removing an electron from a positive ion. The third IE, however, is over five times the previous one. Why is it so much larger? Because the first two electrons are removed from the 3s subshell, but the third electron has to be removed from the n = 2 shell (specifically, the 2p subshell, which is lower in energy than the n = 3 shell). Thus, it takes much more energy than just overcoming a larger ionic charge would suggest. It is trends like this that demonstrate that electrons are organized in atoms in groups.

Example 8.10

Problems

Which atom in each pair has the larger IE?

  1. Ca or Sr
  2. K or K+

Solutions

  1. Because Sr is below Ca on the periodic table, it is easier to remove an electron from it; thus, Ca has the higher IE.
  2. Because K+ has a positive charge, it will be harder to remove another electron from it, so its IE is larger than that of K. Indeed, it will be significantly larger because the next electron in K+ to be removed comes from another shell.

Test Yourself

Which atom has the lower ionization energy, C or F?

Answer

C

Electron Affinity

The opposite of IE is described by electron affinity (EA), which is the energy change when a gas-phase atom accepts an electron:

\ce{A(g)}+\text{e}^-\rightarrow \ce{A^-(g)}\hspace{10 mm}\Delta H\equiv \text{EA}

EA is also usually expressed in kJ/mol. EA also demonstrates some periodic trends, although they are less obvious than the other periodic trends discussed previously. Generally, as you go across the periodic table, EA increases its magnitude:

\text{as }\rightarrow\text{PT, EA}\uparrow

There is not a definitive trend as you go down the periodic table; sometimes EA increases, sometimes it decreases. Figure 8.26 “Electron Affinity on the Periodic Table” shows EA values versus position on the periodic table for the s– and p-block elements. The trend isn’t absolute, especially considering the large positive EA values for the second column. However, the general trend going across the periodic table should be obvious.

Electron affinity on the periodic table. Long description available.
Figure 8.26 “Electron Affinity on the Periodic Table.” Values are in kJ/mol. [Long Description]

Example 8.11

Problems

Predict which atom in each pair will have the highest magnitude of EA.

  1. C or F
  2. Na or S

Solutions

  1. C and F are in the same row on the periodic table, but F is farther to the right. Therefore, F should have the larger magnitude of EA.
  2. Na and S are in the same row on the periodic table, but S is farther to the right. Therefore, S should have the larger magnitude of EA.

Test Yourself

Predict which atom will have the highest magnitude of EA, As or Br.

Answer

Br

Key Takeaways

  • Certain properties — notably effective nuclear charge, atomic radius, IE, and EA — can be qualitatively understood by the positions of the elements on the periodic table.

Exercises

Questions

  1. Write a chemical equation with an IE energy change.
  2. Write a chemical equation with an EA energy change.
  3. State the trends in atomic radii as you go across and down the periodic table.
  4. State the trends in IE as you go across and down the periodic table.
  5. Which atom of each pair is larger?
    1. Na or Cs
    2. N or Bi
  6. Which atom of each pair is larger?
    1. C or Ge
    2. Be or Ba
  7. Which atom of each pair is larger?
    1. K or Cl
    2. Ba or Bi
  8. Which atom of each pair is larger?
    1. Si or S
    2. H or He
  9. Which atom has the higher IE?
    1. Na or S
    2. Ge or Br
  10. Which atom has the higher IE?
    1. C or Ne
    2. Rb or I
  11. Which atom has the higher IE?
    1. Li or Cs
    2. Se or O
  12. Which atom has the higher IE?
    1. Al or Ga
    2. F or I
  13. A third-row element has the following successive IEs: 738; 1,450; 7,734; and 10,550 kJ/mol. Identify the element.
  14. A third-row element has the following successive IEs: 1,012; 1,903; 2,912; 4,940; 6,270; and 21,300 kJ/mol. Identify the element.
  15. For which successive IE is there a large jump in IE for Ca?
  16. For which successive IE is there a large jump in IE for Al?
  17. Which atom has the greater magnitude of EA?
    1. C or F
    2. Al or Cl
  18. Which atom has the greater magnitude of EA?
    1. K or Br
    2. Mg or S

Answers

  1. \ce{Na(g)}\rightarrow \ce{Na^+(g)}+\text{e}^-\hspace{10 mm}\Delta H=\text{IE (answers will vary)}
  1. As you go across, atomic radii decrease; as you go down, atomic radii increase.
    1. Cs
    2. Bi
    1. K
    2. Ba
    1. S
    2. Br
    1. Li
    2. O
  1. Mg
  1. The third IE shows a large jump in Ca.
    1. F
    2. Cl

Long Descriptions

Figure 8.24 description: Chart of atomic radii trends on the periodic table. The data has been compiled in the following table:

Table 8.5 Atomic Radii Trends on the Periodic Table
RowElementAtomic Radius (picometres)
FirstH37
FirstHe31
SecondLi152
SecondBe111
SecondB80
SecondC77
SecondN74
SecondO73
SecondF72
SecondNe71
ThirdNa186
ThirdMg160
ThirdAl143
ThirdSi118
ThirdP110
ThirdS103
ThirdCl100
ThirdAr98
FourthK227
FourthCa197
FourthGa125
FourthGe122
FourthAs120
FourthSe119
FourthBr114
FourthKr112
FifthRb248
FifthSr215
FifthIn167
FifthSn140
FifthSb140
FifthTe142
FifthI133
FifthXe131
SixthCs265
SixthBa222
SixthTi170
SixthPb146
SixthBi150
SixthPo168
SixthAt(140)
SixthRn(141)

[Return to Figure 8.24]

Figure 8.25 description: Chart of ionization energy on the periodic table. The data has been compiled in the following table:

Table 8.6 Ionization Energy on the Periodic Table
RowElementIonization Energy (kJ/mol)
FirstH1312
FirstHe2372
SecondLi520
SecondBe111
SecondB800
SecondC1086
SecondN1402
SecondO1214
SecondF1681
SecondNe2080
ThirdNa496
ThirdMg160
ThirdAl578
ThirdSi786
ThirdP1012
ThirdS1000
ThirdCl1251
ThirdAr1520
FourthK419
FourthCa197
FourthGa579
FourthGe762
FourthAs946
FourthSe940
FourthBr1140
FourthKr1350
FifthRb403
FifthSr550
FifthIn558
FifthSn708
FifthSb833
FifthTe870
FifthI1008
FifthXe1170
SixthCs376
SixthBa503
SixthTi590
SixthPb715
SixthBi703
SixthPo812
SixthAt800
SixthRn1040

[Return to Figure 8.25]

Figure 8.26 description: Chart of electron affinity on the periodic table. The data has been compiled in the following table:

Table 8.7 Electron Affinity on the Periodic Table
RowElementElectron Affinity (kJ/mol)
FirstH−73
SecondLi−60
SecondBe241
SecondB−27
SecondC−122
SecondN~0
SecondO−141
SecondF−328
ThirdNa−53
ThirdMg230
ThirdAl−43
ThirdSi−134
ThirdP−72
ThirdS−200
ThirdCl−349
FourthK−48
FourthCa156
FourthGa−29
FourthGe−119
FourthAs−78
FourthSe−195
FourthBr−325
FifthRb−47
FifthSr167
FifthIn−29
FifthSn−107
FifthSb−103
FifthTe−190
FifthI−295
SixthCs−46
SixthBa52
SixthTi−19
SixthPb−35
SixthBi−35

[Return to Figure 8.26]

Media Attributions

  • “Increasing Effective Nuclear Charge” by Jessie A. Key © CC BY (Attribution)
  • “Atomic Radii Trends on the Periodic Table” by David W. Ball © CC BY-NC-SA (Attribution-NonCommercial-ShareAlike)
  • “Ionization Energy on the Periodic Table” by David W. Ball © CC BY-NC-SA (Attribution-NonCommercial-ShareAlike)

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Copyright © 2014

                                by Jessie A. Key

            Introductory Chemistry - 1st Canadian Edition by Jessie A. Key is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.
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