why can't you convert cis-2-butene

  1. why can't you convert cis-2-butene into trans-2-butene simply by undergoing a rotation?answered the original post. please answer
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    2. Desiree asked by Desiree
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  2. why can't you convert cis-2-butene into trans-2-butene simply by undergoing a rotation/The cis and trans isomers of 2-butene
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    2. Desiree asked by Desiree
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  3. The equilibrium constant, Kp, equals 3.40 for the isomerization reaction:cis-2-butene trans-2-butene. If a flask initially
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    2. Bob asked by Bob
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  4. Consider the isomerization equlibria of an alkene (C4H8) that co-exists as three isomers.(These 3 are in an equlibrium triangle)
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    2. Gleb asked by Gleb
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  5. Which of the following products of the acid-catalyzed elimination of 2-pentanol isthe Hoffmann elimination product? A.
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    2. nilee asked by nilee
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  6. The average bond enthalpy for a C=C double bond is 614kj/mol and that of a C-C single bond is 348kj/mol . Estimate the energy
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    2. tomi asked by tomi
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  7. Which of these names are incorrect?1-butene 2-butene 3-butene I don't know why any of these would be incorrect. Can you explain
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    2. Tabetha asked by Tabetha
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  8. What are the possible reagents needs to transform 1-butene to 2-butene? This can be done in two steps.
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    2. Alice asked by Alice
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  9. why does 2-butene have cis and trans isomers but 1-butene doesn't?
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    2. Ana asked by Ana
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  10. Why is this Alkene structure:CH3 - CH = C - CH3 | Cl called 3, chloro - 2, butene and not 2, chloro - 2, butene? I thought that
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    2. Jakob asked by Jakob
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