Conjugated dienes: Difference between revisions
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imported>Jeanne L. Kuhler (New page: A '''conjugated diene''', such as 1,3-butadiene, has p orbitals located on at least three adjacent atoms, and is more stable than an unconjugated diene, such as 1,4-pentadiene, because i...) |
imported>David E. Volk m (subpages) |
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A '''conjugated diene''', such as 1,3-butadiene, has p orbitals located on at least three adjacent atoms, and is more stable than an unconjugated diene, such as 1,4-pentadiene, because its alternating single and double bonds create a partial double-bond character as a result of resonance. Although 1,4-pentadiene has 2 double bonds, these double bonds are separated by more than one σ bond, making them too far apart to be conjugated and stabilized via resonance. | |||
A '''conjugated diene''', such as 1,3-butadiene, has p orbitals located on at least three adjacent atoms, and is more stable than an unconjugated diene, such as 1,4-pentadiene, because its alternating single and double bonds create a partial double-bond character as a result of resonance. Although 1,4-pentadiene has 2 double bonds, these double bonds are separated by more than one σ bond, making them too far apart to be conjugated and stabilized via resonance. | |||
Latest revision as of 12:24, 20 December 2007
A conjugated diene, such as 1,3-butadiene, has p orbitals located on at least three adjacent atoms, and is more stable than an unconjugated diene, such as 1,4-pentadiene, because its alternating single and double bonds create a partial double-bond character as a result of resonance. Although 1,4-pentadiene has 2 double bonds, these double bonds are separated by more than one σ bond, making them too far apart to be conjugated and stabilized via resonance.