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Chemistry 2e

21.1 Nuclear Structure and Stability

Chemistry 2e21.1 Nuclear Structure and Stability

Table of contents
  1. Preface
  2. 1 Essential Ideas
    1. Introduction
    2. 1.1 Chemistry in Context
    3. 1.2 Phases and Classification of Matter
    4. 1.3 Physical and Chemical Properties
    5. 1.4 Measurements
    6. 1.5 Measurement Uncertainty, Accuracy, and Precision
    7. 1.6 Mathematical Treatment of Measurement Results
    8. Key Terms
    9. Key Equations
    10. Summary
    11. Exercises
  3. 2 Atoms, Molecules, and Ions
    1. Introduction
    2. 2.1 Early Ideas in Atomic Theory
    3. 2.2 Evolution of Atomic Theory
    4. 2.3 Atomic Structure and Symbolism
    5. 2.4 Chemical Formulas
    6. 2.5 The Periodic Table
    7. 2.6 Ionic and Molecular Compounds
    8. 2.7 Chemical Nomenclature
    9. Key Terms
    10. Key Equations
    11. Summary
    12. Exercises
  4. 3 Composition of Substances and Solutions
    1. Introduction
    2. 3.1 Formula Mass and the Mole Concept
    3. 3.2 Determining Empirical and Molecular Formulas
    4. 3.3 Molarity
    5. 3.4 Other Units for Solution Concentrations
    6. Key Terms
    7. Key Equations
    8. Summary
    9. Exercises
  5. 4 Stoichiometry of Chemical Reactions
    1. Introduction
    2. 4.1 Writing and Balancing Chemical Equations
    3. 4.2 Classifying Chemical Reactions
    4. 4.3 Reaction Stoichiometry
    5. 4.4 Reaction Yields
    6. 4.5 Quantitative Chemical Analysis
    7. Key Terms
    8. Key Equations
    9. Summary
    10. Exercises
  6. 5 Thermochemistry
    1. Introduction
    2. 5.1 Energy Basics
    3. 5.2 Calorimetry
    4. 5.3 Enthalpy
    5. Key Terms
    6. Key Equations
    7. Summary
    8. Exercises
  7. 6 Electronic Structure and Periodic Properties of Elements
    1. Introduction
    2. 6.1 Electromagnetic Energy
    3. 6.2 The Bohr Model
    4. 6.3 Development of Quantum Theory
    5. 6.4 Electronic Structure of Atoms (Electron Configurations)
    6. 6.5 Periodic Variations in Element Properties
    7. Key Terms
    8. Key Equations
    9. Summary
    10. Exercises
  8. 7 Chemical Bonding and Molecular Geometry
    1. Introduction
    2. 7.1 Ionic Bonding
    3. 7.2 Covalent Bonding
    4. 7.3 Lewis Symbols and Structures
    5. 7.4 Formal Charges and Resonance
    6. 7.5 Strengths of Ionic and Covalent Bonds
    7. 7.6 Molecular Structure and Polarity
    8. Key Terms
    9. Key Equations
    10. Summary
    11. Exercises
  9. 8 Advanced Theories of Covalent Bonding
    1. Introduction
    2. 8.1 Valence Bond Theory
    3. 8.2 Hybrid Atomic Orbitals
    4. 8.3 Multiple Bonds
    5. 8.4 Molecular Orbital Theory
    6. Key Terms
    7. Key Equations
    8. Summary
    9. Exercises
  10. 9 Gases
    1. Introduction
    2. 9.1 Gas Pressure
    3. 9.2 Relating Pressure, Volume, Amount, and Temperature: The Ideal Gas Law
    4. 9.3 Stoichiometry of Gaseous Substances, Mixtures, and Reactions
    5. 9.4 Effusion and Diffusion of Gases
    6. 9.5 The Kinetic-Molecular Theory
    7. 9.6 Non-Ideal Gas Behavior
    8. Key Terms
    9. Key Equations
    10. Summary
    11. Exercises
  11. 10 Liquids and Solids
    1. Introduction
    2. 10.1 Intermolecular Forces
    3. 10.2 Properties of Liquids
    4. 10.3 Phase Transitions
    5. 10.4 Phase Diagrams
    6. 10.5 The Solid State of Matter
    7. 10.6 Lattice Structures in Crystalline Solids
    8. Key Terms
    9. Key Equations
    10. Summary
    11. Exercises
  12. 11 Solutions and Colloids
    1. Introduction
    2. 11.1 The Dissolution Process
    3. 11.2 Electrolytes
    4. 11.3 Solubility
    5. 11.4 Colligative Properties
    6. 11.5 Colloids
    7. Key Terms
    8. Key Equations
    9. Summary
    10. Exercises
  13. 12 Kinetics
    1. Introduction
    2. 12.1 Chemical Reaction Rates
    3. 12.2 Factors Affecting Reaction Rates
    4. 12.3 Rate Laws
    5. 12.4 Integrated Rate Laws
    6. 12.5 Collision Theory
    7. 12.6 Reaction Mechanisms
    8. 12.7 Catalysis
    9. Key Terms
    10. Key Equations
    11. Summary
    12. Exercises
  14. 13 Fundamental Equilibrium Concepts
    1. Introduction
    2. 13.1 Chemical Equilibria
    3. 13.2 Equilibrium Constants
    4. 13.3 Shifting Equilibria: Le Châtelier’s Principle
    5. 13.4 Equilibrium Calculations
    6. Key Terms
    7. Key Equations
    8. Summary
    9. Exercises
  15. 14 Acid-Base Equilibria
    1. Introduction
    2. 14.1 Brønsted-Lowry Acids and Bases
    3. 14.2 pH and pOH
    4. 14.3 Relative Strengths of Acids and Bases
    5. 14.4 Hydrolysis of Salts
    6. 14.5 Polyprotic Acids
    7. 14.6 Buffers
    8. 14.7 Acid-Base Titrations
    9. Key Terms
    10. Key Equations
    11. Summary
    12. Exercises
  16. 15 Equilibria of Other Reaction Classes
    1. Introduction
    2. 15.1 Precipitation and Dissolution
    3. 15.2 Lewis Acids and Bases
    4. 15.3 Coupled Equilibria
    5. Key Terms
    6. Key Equations
    7. Summary
    8. Exercises
  17. 16 Thermodynamics
    1. Introduction
    2. 16.1 Spontaneity
    3. 16.2 Entropy
    4. 16.3 The Second and Third Laws of Thermodynamics
    5. 16.4 Free Energy
    6. Key Terms
    7. Key Equations
    8. Summary
    9. Exercises
  18. 17 Electrochemistry
    1. Introduction
    2. 17.1 Review of Redox Chemistry
    3. 17.2 Galvanic Cells
    4. 17.3 Electrode and Cell Potentials
    5. 17.4 Potential, Free Energy, and Equilibrium
    6. 17.5 Batteries and Fuel Cells
    7. 17.6 Corrosion
    8. 17.7 Electrolysis
    9. Key Terms
    10. Key Equations
    11. Summary
    12. Exercises
  19. 18 Representative Metals, Metalloids, and Nonmetals
    1. Introduction
    2. 18.1 Periodicity
    3. 18.2 Occurrence and Preparation of the Representative Metals
    4. 18.3 Structure and General Properties of the Metalloids
    5. 18.4 Structure and General Properties of the Nonmetals
    6. 18.5 Occurrence, Preparation, and Compounds of Hydrogen
    7. 18.6 Occurrence, Preparation, and Properties of Carbonates
    8. 18.7 Occurrence, Preparation, and Properties of Nitrogen
    9. 18.8 Occurrence, Preparation, and Properties of Phosphorus
    10. 18.9 Occurrence, Preparation, and Compounds of Oxygen
    11. 18.10 Occurrence, Preparation, and Properties of Sulfur
    12. 18.11 Occurrence, Preparation, and Properties of Halogens
    13. 18.12 Occurrence, Preparation, and Properties of the Noble Gases
    14. Key Terms
    15. Summary
    16. Exercises
  20. 19 Transition Metals and Coordination Chemistry
    1. Introduction
    2. 19.1 Occurrence, Preparation, and Properties of Transition Metals and Their Compounds
    3. 19.2 Coordination Chemistry of Transition Metals
    4. 19.3 Spectroscopic and Magnetic Properties of Coordination Compounds
    5. Key Terms
    6. Summary
    7. Exercises
  21. 20 Organic Chemistry
    1. Introduction
    2. 20.1 Hydrocarbons
    3. 20.2 Alcohols and Ethers
    4. 20.3 Aldehydes, Ketones, Carboxylic Acids, and Esters
    5. 20.4 Amines and Amides
    6. Key Terms
    7. Summary
    8. Exercises
  22. 21 Nuclear Chemistry
    1. Introduction
    2. 21.1 Nuclear Structure and Stability
    3. 21.2 Nuclear Equations
    4. 21.3 Radioactive Decay
    5. 21.4 Transmutation and Nuclear Energy
    6. 21.5 Uses of Radioisotopes
    7. 21.6 Biological Effects of Radiation
    8. Key Terms
    9. Key Equations
    10. Summary
    11. Exercises
  23. A | The Periodic Table
  24. B | Essential Mathematics
  25. C | Units and Conversion Factors
  26. D | Fundamental Physical Constants
  27. E | Water Properties
  28. F | Composition of Commercial Acids and Bases
  29. G | Standard Thermodynamic Properties for Selected Substances
  30. H | Ionization Constants of Weak Acids
  31. I | Ionization Constants of Weak Bases
  32. J | Solubility Products
  33. K | Formation Constants for Complex Ions
  34. L | Standard Electrode (Half-Cell) Potentials
  35. M | Half-Lives for Several Radioactive Isotopes
  36. Answer Key
    1. Chapter 1
    2. Chapter 2
    3. Chapter 3
    4. Chapter 4
    5. Chapter 5
    6. Chapter 6
    7. Chapter 7
    8. Chapter 8
    9. Chapter 9
    10. Chapter 10
    11. Chapter 11
    12. Chapter 12
    13. Chapter 13
    14. Chapter 14
    15. Chapter 15
    16. Chapter 16
    17. Chapter 17
    18. Chapter 18
    19. Chapter 19
    20. Chapter 20
    21. Chapter 21
  37. Index

Learning Objectives

By the end of this section, you will be able to:

  • Describe nuclear structure in terms of protons, neutrons, and electrons
  • Calculate mass defect and binding energy for nuclei
  • Explain trends in the relative stability of nuclei

Nuclear chemistry is the study of reactions that involve changes in nuclear structure. The chapter on atoms, molecules, and ions introduced the basic idea of nuclear structure, that the nucleus of an atom is composed of protons and, with the exception of 11H,11H, neutrons. Recall that the number of protons in the nucleus is called the atomic number (Z) of the element, and the sum of the number of protons and the number of neutrons is the mass number (A). Atoms with the same atomic number but different mass numbers are isotopes of the same element. When referring to a single type of nucleus, we often use the term nuclide and identify it by the notation ZAX,ZAX, where X is the symbol for the element, A is the mass number, and Z is the atomic number (for example, 614C).614C). Often a nuclide is referenced by the name of the element followed by a hyphen and the mass number. For example, 614C614C is called “carbon-14.”

Protons and neutrons, collectively called nucleons, are packed together tightly in a nucleus. With a radius of about 10−15 meters, a nucleus is quite small compared to the radius of the entire atom, which is about 10−10 meters. Nuclei are extremely dense compared to bulk matter, averaging 1.8 ×× 1014 grams per cubic centimeter. For example, water has a density of 1 gram per cubic centimeter, and iridium, one of the densest elements known, has a density of 22.6 g/cm3. If the earth’s density were equal to the average nuclear density, the earth’s radius would be only about 200 meters (earth’s actual radius is approximately 6.4 ×× 106 meters, 30,000 times larger). Example 21.1 demonstrates just how great nuclear densities can be in the natural world.

Example 21.1

Density of a Neutron Star

Neutron stars form when the core of a very massive star undergoes gravitational collapse, causing the star’s outer layers to explode in a supernova. Composed almost completely of neutrons, they are the densest-known stars in the universe, with densities comparable to the average density of an atomic nucleus. A neutron star in a faraway galaxy has a mass equal to 2.4 solar masses (1 solar mass = MM = mass of the sun = 1.99 ×× 1030 kg) and a diameter of 26 km.

(a) What is the density of this neutron star?

(b) How does this neutron star’s density compare to the density of a uranium nucleus, which has a diameter of about 15 fm (1 fm = 10–15 m)?


We can treat both the neutron star and the U-235 nucleus as spheres. Then the density for both is given by:

(a) The radius of the neutron star is 12×26 km=12×2.6×104m=1.3×104m,12×26 km=12×2.6×104m=1.3×104m, so the density of the neutron star is:


(b) The radius of the U-235 nucleus is 12×15×10−15m=7.5×10−15m,12×15×10−15m=7.5×10−15m, so the density of the U-235 nucleus is:

d=mV=m43πr3=235 amu(1.66×10−27kg1 amu)43π(7.5×10−15m)3=2.2×1017kg/m3d=mV=m43πr3=235 amu(1.66×10−27kg1 amu)43π(7.5×10−15m)3=2.2×1017kg/m3

These values are fairly similar (same order of magnitude), but the neutron star is more than twice as dense as the U-235 nucleus.

Check Your Learning

Find the density of a neutron star with a mass of 1.97 solar masses and a diameter of 13 km, and compare it to the density of a hydrogen nucleus, which has a diameter of 1.75 fm (1 fm = 1 ×× 10–15 m).


The density of the neutron star is 3.4 ×× 1018 kg/m3. The density of a hydrogen nucleus is 6.0 ×× 1017 kg/m3. The neutron star is 5.7 times denser than the hydrogen nucleus.

To hold positively charged protons together in the very small volume of a nucleus requires very strong attractive forces because the positively charged protons repel one another strongly at such short distances. The force of attraction that holds the nucleus together is the strong nuclear force. (The strong force is one of the four fundamental forces that are known to exist. The others are the electromagnetic force, the gravitational force, and the nuclear weak force.) This force acts between protons, between neutrons, and between protons and neutrons. It is very different from the electrostatic force that holds negatively charged electrons around a positively charged nucleus (the attraction between opposite charges). Over distances less than 10−15 meters and within the nucleus, the strong nuclear force is much stronger than electrostatic repulsions between protons; over larger distances and outside the nucleus, it is essentially nonexistent.

Nuclear Binding Energy

As a simple example of the energy associated with the strong nuclear force, consider the helium atom composed of two protons, two neutrons, and two electrons. The total mass of these six subatomic particles may be calculated as:

(2×1.0073 amu)+(2×1.0087 amu)+(2×0.00055 amu)=4.0331 amuprotonsneutronselectrons(2×1.0073 amu)+(2×1.0087 amu)+(2×0.00055 amu)=4.0331 amuprotonsneutronselectrons

However, mass spectrometric measurements reveal that the mass of an 24He24He atom is 4.0026 amu, less than the combined masses of its six constituent subatomic particles. This difference between the calculated and experimentally measured masses is known as the mass defect of the atom. In the case of helium, the mass defect indicates a “loss” in mass of 4.0331 amu – 4.0026 amu = 0.0305 amu. The loss in mass accompanying the formation of an atom from protons, neutrons, and electrons is due to the conversion of that mass into energy that is evolved as the atom forms. The nuclear binding energy is the energy produced when the atoms’ nucleons are bound together; this is also the energy needed to break a nucleus into its constituent protons and neutrons. In comparison to chemical bond energies, nuclear binding energies are vastly greater, as we will learn in this section. Consequently, the energy changes associated with nuclear reactions are vastly greater than are those for chemical reactions.

The conversion between mass and energy is most identifiably represented by the mass-energy equivalence equation as stated by Albert Einstein:


where E is energy, m is mass of the matter being converted, and c is the speed of light in a vacuum. This equation can be used to find the amount of energy that results when matter is converted into energy. Using this mass-energy equivalence equation, the nuclear binding energy of a nucleus may be calculated from its mass defect, as demonstrated in Example 21.2. A variety of units are commonly used for nuclear binding energies, including electron volts (eV), with 1 eV equaling the amount of energy necessary to the move the charge of an electron across an electric potential difference of 1 volt, making 1 eV = 1.602 ×× 10–19 J.

Example 21.2

Calculation of Nuclear Binding Energy

Determine the binding energy for the nuclide 24He24He in:

(a) joules per mole of nuclei

(b) joules per nucleus

(c) MeV per nucleus


The mass defect for a 24He24He nucleus is 0.0305 amu, as shown previously. Determine the binding energy in joules per nuclide using the mass-energy equivalence equation. To accommodate the requested energy units, the mass defect must be expressed in kilograms (recall that 1 J = 1 kg m2/s2).

(a) First, express the mass defect in g/mol. This is easily done considering the numerical equivalence of atomic mass (amu) and molar mass (g/mol) that results from the definitions of the amu and mole units (refer to the previous discussion in the chapter on atoms, molecules, and ions if needed). The mass defect is therefore 0.0305 g/mol. To accommodate the units of the other terms in the mass-energy equation, the mass must be expressed in kg, since 1 J = 1 kg m2/s2. Converting grams into kilograms yields a mass defect of 3.05 ×× 10–5 kg/mol. Substituting this quantity into the mass-energy equivalence equation yields:

E=mc2=3.05×10−5kgmol×(2.998×108ms)2=2.74×1012kgm2s−2mol−1=2.74×1012Jmol−1=2.74 TJ mol−1E=mc2=3.05×10−5kgmol×(2.998×108ms)2=2.74×1012kgm2s−2mol−1=2.74×1012Jmol−1=2.74 TJ mol−1

Note that this tremendous amount of energy is associated with the conversion of a very small amount of matter (about 30 mg, roughly the mass of typical drop of water).

(b) The binding energy for a single nucleus is computed from the molar binding energy using Avogadro’s number:

E=2.74×1012Jmol−1×1 mol6.022×1023nuclei=4.55×10−12J=4.55 pJE=2.74×1012Jmol−1×1 mol6.022×1023nuclei=4.55×10−12J=4.55 pJ

(c) Recall that 1 eV = 1.602 ×× 10–19 J. Using the binding energy computed in part (b):

E=4.55×10−12J×1 eV1.602×10−19J=2.84×107eV=28.4 MeVE=4.55×10−12J×1 eV1.602×10−19J=2.84×107eV=28.4 MeV

Check Your Learning

What is the binding energy for the nuclide 919F919F (atomic mass: 18.9984 amu) in MeV per nucleus?


148.4 MeV

Because the energy changes for breaking and forming bonds are so small compared to the energy changes for breaking or forming nuclei, the changes in mass during all ordinary chemical reactions are virtually undetectable. As described in the chapter on thermochemistry, the most energetic chemical reactions exhibit enthalpies on the order of thousands of kJ/mol, which is equivalent to mass differences in the nanogram range (10–9 g). On the other hand, nuclear binding energies are typically on the order of billions of kJ/mol, corresponding to mass differences in the milligram range (10–3 g).

Nuclear Stability

A nucleus is stable if it cannot be transformed into another configuration without adding energy from the outside. Of the thousands of nuclides that exist, about 250 are stable. A plot of the number of neutrons versus the number of protons for stable nuclei reveals that the stable isotopes fall into a narrow band. This region is known as the band of stability (also called the belt, zone, or valley of stability). The straight line in Figure 21.2 represents nuclei that have a 1:1 ratio of protons to neutrons (n:p ratio). Note that the lighter stable nuclei, in general, have equal numbers of protons and neutrons. For example, nitrogen-14 has seven protons and seven neutrons. Heavier stable nuclei, however, have increasingly more neutrons than protons. For example: iron-56 has 30 neutrons and 26 protons, an n:p ratio of 1.15, whereas the stable nuclide lead-207 has 125 neutrons and 82 protons, an n:p ratio equal to 1.52. This is because larger nuclei have more proton-proton repulsions, and require larger numbers of neutrons to provide compensating strong forces to overcome these electrostatic repulsions and hold the nucleus together.

A graph is shown where the x-axis is labeled “Number of neutrons, open parenthesis, n, close parenthesis” and has values of 0 to 180 in increments of 10. The y-axis is labeled “Number of protons, open parenthesis, Z, close parenthesis” and has values of 0 to 120 in increments of 10. A green shaded band of varying width, labeled “Radioactive,” extends from point 0 on both axes to 178 on the y-axis and 118 on the x-axis in a linear manner. The width of this band varies from 8 to 18 units in width according to the x-axis measurements. A blue line in a roughly zig-zag pattern runs through the middle of the shaded band and stops at 128 on the y-axis and 82 on the x-axis. This line is labeled “Nonradioactive.” An unlabeled, black, solid line extends from point 0, 0 to 120, 120 in a linear manner.
Figure 21.2 This plot shows the nuclides that are known to exist and those that are stable. The stable nuclides are indicated in blue, and the unstable nuclides are indicated in green. Note that all isotopes of elements with atomic numbers greater than 83 are unstable. The solid line is the line where n = Z.

The nuclei that are to the left or to the right of the band of stability are unstable and exhibit radioactivity. They change spontaneously (decay) into other nuclei that are either in, or closer to, the band of stability. These nuclear decay reactions convert one unstable isotope (or radioisotope) into another, more stable, isotope. We will discuss the nature and products of this radioactive decay in subsequent sections of this chapter.

Several observations may be made regarding the relationship between the stability of a nucleus and its structure. Nuclei with even numbers of protons, neutrons, or both are more likely to be stable (see Table 21.1). Nuclei with certain numbers of nucleons, known as magic numbers, are stable against nuclear decay. These numbers of protons or neutrons (2, 8, 20, 28, 50, 82, and 126) make complete shells in the nucleus. These are similar in concept to the stable electron shells observed for the noble gases. Nuclei that have magic numbers of both protons and neutrons, such as 24He,24He, 816O,816O, 2040Ca,2040Ca, and 82208Pb,82208Pb, are called “double magic” and are particularly stable. These trends in nuclear stability may be rationalized by considering a quantum mechanical model of nuclear energy states analogous to that used to describe electronic states earlier in this textbook. The details of this model are beyond the scope of this chapter.

Stable Nuclear Isotopes
Number of Stable Isotopes Proton Number Neutron Number
157 even even
53 even odd
50 odd even
5 odd odd
Table 21.1

The relative stability of a nucleus is correlated with its binding energy per nucleon, the total binding energy for the nucleus divided by the number or nucleons in the nucleus. For instance, we saw in Example 21.2 that the binding energy for a 24He24He nucleus is 28.4 MeV. The binding energy per nucleon for a 24He24He nucleus is therefore:

28.4 MeV4 nucleons=7.10 MeV/nucleon28.4 MeV4 nucleons=7.10 MeV/nucleon

In Example 21.3, we learn how to calculate the binding energy per nucleon of a nuclide on the curve shown in Figure 21.3.

A graph is shown where the x-axis is labeled “binding energy per nucleon, open parenthesis, M e V, close parenthesis” and has values of 0 to 10 in increments of 1. The y-axis is labeled “Mass number” and has values of 0 to 260 in increments of 20. A line of best fit beginning at point 0, 0 is drawn through points “8, 5.5; 9, 7.3; 18, 7.1; 20, 7.5; 19, 7.9; 27, 7.8; 21, 8.1; 25, 8.4; 37, 8.6; 43, 8.8; 57, 8.6; 60, 8.9; 70, 9; 88, 8.8; 102, 8.9; 108, 8.5; 126, 8.7; 133, 8.8; 143, 8.2; 157, 8.1; 167, 8.2; 195, 7.9; 205, 7.9; 241, 7.3 and 255, 75. An upward-facing arrow near the bottom left of the graph is labeled “Fusion” while a left-facing arrow near the top right is labeled “Fission.”
Figure 21.3 The binding energy per nucleon is largest for nuclides with mass number of approximately 56.

Example 21.3

Calculation of Binding Energy per Nucleon

The iron nuclide 2656Fe2656Fe lies near the top of the binding energy curve (Figure 21.3) and is one of the most stable nuclides. What is the binding energy per nucleon (in MeV) for the nuclide 2656Fe2656Fe (atomic mass of 55.9349 amu)?


As in Example 21.2, we first determine the mass defect of the nuclide, which is the difference between the mass of 26 protons, 30 neutrons, and 26 electrons, and the observed mass of an 2656Fe2656Fe atom:
Mass defect=[(26×1.0073 amu)+(30×1.0087 amu)+(26×0.00055 amu)]55.9349 amu=56.4651 amu55.9349 amu=0.5302 amuMass defect=[(26×1.0073 amu)+(30×1.0087 amu)+(26×0.00055 amu)]55.9349 amu=56.4651 amu55.9349 amu=0.5302 amu

We next calculate the binding energy for one nucleus from the mass defect using the mass-energy equivalence equation:

E=mc2=0.5302 amu×1.6605×10−27kg1 amu×(2.998×108m/s)2=7.913×10−11kgm/s2=7.913×10−11JE=mc2=0.5302 amu×1.6605×10−27kg1 amu×(2.998×108m/s)2=7.913×10−11kgm/s2=7.913×10−11J

We then convert the binding energy in joules per nucleus into units of MeV per nuclide:

7.913×10−11J×1 MeV1.602×10−13J=493.9 MeV7.913×10−11J×1 MeV1.602×10−13J=493.9 MeV

Finally, we determine the binding energy per nucleon by dividing the total nuclear binding energy by the number of nucleons in the atom:

Binding energy per nucleon=493.9 MeV56=8.820 MeV/nucleonBinding energy per nucleon=493.9 MeV56=8.820 MeV/nucleon

Note that this is almost 25% larger than the binding energy per nucleon for 24He.24He.

(Note also that this is the same process as in Example 21.1, but with the additional step of dividing the total nuclear binding energy by the number of nucleons.)

Check Your Learning

What is the binding energy per nucleon in 919F919F (atomic mass, 18.9984 amu)?


7.810 MeV/nucleon

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