Asked by Sam

Why is (E)-1,2-diisopropylethene more stable than (Z)-1,2-diisopropylethene? Why are they more stable than 1,1-diisopropylethe?

And doesn't the bond angle between the C=C-C carbons increase with (Z)-1,2-diisopropylethene > (E)-1,2-diisopropylethene > 1,1-diisopropylethe? So why isn't the same as (E) being greater than (Z)?

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