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SCIENCE · INVESTIGATE AND EXPLAIN

Distinguish bond depth, equilibrium and restoring slope

Use a supplied energy landscape without turning its shape into an unverified molecular measurement.

Learning outcome: Capture x=.8,1,1.5 at D=400. Predict slope signs and restoring directions. Change depth to600 at fixed x and separate energy scaling from equilibrium-position change.

Starting recap

Review the atomic electron ledger, signed energy changes and dimensional conversions. Distinguish a mathematical parameter from a unique material identification.

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Try

For D=400 kJ/mol at x=1, U=−400 and slope=0. At x=1.5, U≈−240.17 kJ/mol, so the system is159.83 kJ/mol above the minimum.

Open the experiment

Predict

Can a bound equilibrium have zero net force and still require energy to separate its atoms?

Experiment

Capture x=.8,1,1.5 at D=400. Predict slope signs and restoring directions. Change depth to600 at fixed x and separate energy scaling from equilibrium-position change.

Read a bond-energy landscape

Worked teaching model · synthetic values · Original dimensionless Morse-shaped potential U=D[(1−exp(−2(x−1)))²−1], x=r/re. Zero is separated atoms, minimum −D at x=1. A supplied shape, not a quantum calculation, finite-temperature dissociation enthalpy or molecular dynamics trajectory. Local slope is reported per unit dimensionless x.

Reset keeps your prediction, captures and practice history.

potential energy (kJ/mol)separation ratio r/re040.01-400

Axes rescale with settings. Compare numerical values, not screen slopes. Discrete stems show steps, contributors or partial sums; connected samples show the declared parameter relationship, not a measured time trajectory.

Numerical diagram coordinates
separation ratio r/repotential energy (kJ/mol)
0.7-129.6483
0.75-231.6643
0.8-303.2434
0.85-351.0395
0.9-380.3923
0.95-395.5756
1-400
1.05-396.3776
1.1-386.8566
1.15-373.1299
1.2-356.5245
1.25-338.0728
1.3-318.5716
1.35-298.6295
1.4-278.7046
1.45-259.1362
1.5-240.1694
1.55-221.9756
1.6-204.6682
1.65-188.316
1.7-172.9535
1.75-158.5893
1.8-145.2123
1.85-132.7975
1.9-121.3096
1.95-110.7066
2-100.942
2.05-91.96691
2.1-83.73159
2.15-76.18634
2.2-69.28246
2.25-62.97282
2.3-57.21224
2.35-51.95778
2.4-47.1689
2.45-42.80755
2.5-38.83815
2.55-35.22759
2.6-31.94514
2.65-28.96239
2.7-26.25311
2.75-23.79315
2.8-21.56034
2.85-19.53432
2.9-17.69644
2.95-16.02964
3-14.51833
3.05-13.14828
3.1-11.90651
3.15-10.7812
3.2-9.761579
3.25-8.837833
3.3-8.001053
3.35-7.243132
3.4-6.556706
3.45-5.935086
3.5-5.372198
3.55-4.862529
3.6-4.401079
3.65-3.983309
3.7-3.605105
3.75-3.262736
3.8-2.952821
3.85-2.672294
3.9-2.418377
3.95-2.188554
4-1.980544
Calculated values under declared assumptions
QuantityValueUnit
Potential energy-400kJ/mol
Energy above minimum0kJ/mol
Local potential slope0kJ/mol per x
Minimum-to-separated energy400kJ/mol

The minimum fixes equilibrium separation; depth and slope describe different properties.

A positive slope at stretched separation means a restoring force toward smaller r; a negative slope on the compressed side means repulsion. Force is minus the slope with respect to actual distance, so the displayed dimensionless-coordinate slope is not a force in newtons. At the minimum force is zero but the bond is not absent.

Capture contrasting evidence and retain the interpretation limits. These supplied models do not identify an actual material or certify practical laboratory skill.

The minimum fixes equilibrium separation; depth and slope describe different properties.

A positive slope at stretched separation means a restoring force toward smaller r; a negative slope on the compressed side means repulsion. Force is minus the slope with respect to actual distance, so the displayed dimensionless-coordinate slope is not a force in newtons. At the minimum force is zero but the bond is not absent.

Captures preserve recipes and replay their calculated results. They are synthetic model evidence, not physical measurements.

Understand

Energy is not force

A stable bond balances competing effects: electron-nuclear attraction and repulsive contributions produce an energy minimum at a finite separation. Force depends on the direction of energy change with distance, not on whether potential energy is positive or negative. Choosing zero at separated atoms makes a bound minimum negative; changing the reference would not change forces.

Read the supplied landscape

Use x=r/re and U=D[(1−exp(−2(x−1)))²−1]. This is an original parameterized Morse-shaped teaching potential. At x=1, the exponential is one, so U=−D. Far apart, the exponential tends to zero, and U approaches zero. The depth D is thus the minimum-to-asymptote energy, not the slope or equilibrium distance.

Interpret the two sides

On the stretched side, U rises with increasing separation. The force points toward smaller r, opposing the stretch. On the compressed side, increasing r lowers U, so the force points outward. The ledger supplies the local slope with respect to dimensionless x; it is not a force in newtons. To obtain a force one would need the actual distance scale and energy per molecule, not simply attach force units to a molar energy slope.

Work an original comparison

For D=400 kJ/mol, x=1 gives −400 kJ/mol. At x=1.5, exp(−1)≈.36788 and U≈−240.17 kJ/mol. Raising the separation from the minimum to that point increases potential energy by about159.83 kJ/mol. A deeper D=600 well scales these energies by1.5 without changing the model’s minimum at x=1.

State the limit of the evidence

The nuclei do not actually sit motionless at the minimum in the lowest quantum vibrational state. Zero-point energy and thermal corrections distinguish a well depth from experimentally defined dissociation quantities. This module does not calculate vibrational levels or trajectories. Compare two curves with the same depth but different widths conceptually: they could have the same minimum-to-asymptote energy and different stiffness. Depth alone cannot determine every bonding property.

Evidence and safety boundary

Conceptual sources checked 30 October 2026: NIST Morse potential, Bond energetics. All prose, numerical packets and diagrams are original; no textbook exercises or images are reproduced. The activity is supplied mathematical or synthetic evidence, not a performed materials experiment. No unknown substances, heating, high voltage or chemical synthesis are requested. Retain prior predictions and a changed-case explanation; numerical agreement alone does not certify independent understanding or practical competence.

Apply

At the potential minimum, which statement is correct?

Public practice checks a specific claim. It does not establish independent mastery.

Explain why well depth is not automatically the finite-temperature bond dissociation enthalpy.

Continue

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