600 500 400 Reactant 300 200 E, = 435 10 J 2 100 아 Initial state AE7X 10J -30 0° 30 60 90 120 150° 180 210 Reaction progress (angle of twist) Cis-2-butene is one of two forms of butene where the middle two carbon atoms are joined by a double bond. The other form is trans-2-butene. The conversion of the cis form to the trans form is slow at room temperature, and the two forms represent two distinct compounds. Conversion of the cis to the trans form involves rotation about the C-C double bond, which requires a substantial amount of energy on the molecular scale. Move the slider to observe the different conformations and their energies along the pathway of the conversion. Consider the linkage between the two central C atoms in cis-2-butene. How many sigma bonds join these two C atoms? Potential Energy 10 J

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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600
500
400
Reactant
300
画 200
E, = 435 10J
2 100
아--
Initial state
AE-7X 10 J
-30
0°
30
60
90
120
150°
180
210
Reaction progress (angle of twist)
Cis-2-butene is one of two forms of butene where the middle two carbon atoms are joined by a double bond. The other form is trans-2-butene. The conversion of the cis
form to the trans form is slow at room temperature, and the two forms represent two distinct compounds. Conversion of the cis to the trans form involves rotation about
the C-C double bond, which requires a substantial amount of energy on the molecular scale. Move the slider to observe the different conformations and their energies along
the pathway of the conversion.
Consider the linkage between the two central C atoms in cis-2-butene. How many sigma bonds join these two C atoms?
Potential Energy 10 J
Transcribed Image Text:600 500 400 Reactant 300 画 200 E, = 435 10J 2 100 아-- Initial state AE-7X 10 J -30 0° 30 60 90 120 150° 180 210 Reaction progress (angle of twist) Cis-2-butene is one of two forms of butene where the middle two carbon atoms are joined by a double bond. The other form is trans-2-butene. The conversion of the cis form to the trans form is slow at room temperature, and the two forms represent two distinct compounds. Conversion of the cis to the trans form involves rotation about the C-C double bond, which requires a substantial amount of energy on the molecular scale. Move the slider to observe the different conformations and their energies along the pathway of the conversion. Consider the linkage between the two central C atoms in cis-2-butene. How many sigma bonds join these two C atoms? Potential Energy 10 J
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