ggrree
  • ggrree
Hey, I'm having trouble understanding a result of a chemist lab which involved computing the energies of molecules using software. I found the energies of (Z)- 1,1 diisopropyl ethene, (E) 1,1 diisopropyl ethene and 1,1 diisopropyl ethane to be -102.10 , -102.17, and -89.49 kJ/mol, respectively. I understand why the E isomer is more stable than the Z isomer, but why is the 1,1 diisopropyl ethane less stable than both of the others?
Chemistry
  • Stacey Warren - Expert brainly.com
Hey! We 've verified this expert answer for you, click below to unlock the details :)
SOLVED
At vero eos et accusamus et iusto odio dignissimos ducimus qui blanditiis praesentium voluptatum deleniti atque corrupti quos dolores et quas molestias excepturi sint occaecati cupiditate non provident, similique sunt in culpa qui officia deserunt mollitia animi, id est laborum et dolorum fuga. Et harum quidem rerum facilis est et expedita distinctio. Nam libero tempore, cum soluta nobis est eligendi optio cumque nihil impedit quo minus id quod maxime placeat facere possimus, omnis voluptas assumenda est, omnis dolor repellendus. Itaque earum rerum hic tenetur a sapiente delectus, ut aut reiciendis voluptatibus maiores alias consequatur aut perferendis doloribus asperiores repellat.
chestercat
  • chestercat
I got my questions answered at brainly.com in under 10 minutes. Go to brainly.com now for free help!
ggrree
  • ggrree
I was thinking that the ability to rotate around the single bond would allow it to reduce any steric stress, but this isn't reflected in the software. Why is this?

Looking for something else?

Not the answer you are looking for? Search for more explanations.