T Tina324 Full Member 10+ Year Member 15+ Year Member Joined May 7, 2008 Messages 198 Reaction score 0 Points 0 Pre-Dental Sep 2, 2008 #1 Advertisement - Members don't see this ad cyclopropene= not aromatic because the carbon opposite the double bond is sp3? cyclopropene with a positive charge opposite the double bond=aromatic because it is sp2 with an empty p orbital?
Advertisement - Members don't see this ad cyclopropene= not aromatic because the carbon opposite the double bond is sp3? cyclopropene with a positive charge opposite the double bond=aromatic because it is sp2 with an empty p orbital?
U UCfan Full Member 10+ Year Member 15+ Year Member Joined Jul 30, 2008 Messages 237 Reaction score 0 Points 0 Location Michigan Dental Student Sep 2, 2008 #2 If an H- ion is removed from that third carbon then there will be an unoccupied p-orbital. For this reason, it is aromatic. Upvote 0 Downvote
If an H- ion is removed from that third carbon then there will be an unoccupied p-orbital. For this reason, it is aromatic.
T Tina324 Full Member 10+ Year Member 15+ Year Member Joined May 7, 2008 Messages 198 Reaction score 0 Points 0 Pre-Dental Sep 2, 2008 #3 so cyclopropene with ALL of its H's...does NOT have a continuous pi system..correct? Upvote 0 Downvote
J JBarr29 Full Member 10+ Year Member 5+ Year Member 15+ Year Member Joined Aug 15, 2008 Messages 132 Reaction score 0 Points 0 Dental Student Sep 3, 2008 #4 because it will have sp3 carbon when no Hs are removed....makes it non aromatic Upvote 0 Downvote
keliao Full Member 10+ Year Member 15+ Year Member Joined Jun 10, 2008 Messages 344 Reaction score 0 Points 0 Location NorthEast Pre-Dental Sep 3, 2008 #5 cyclopropene (non-aro due to sp3) cyclopropene with a lone pair ( anti-aro) cyclopropene with positive charge (non-aro) Upvote 0 Downvote
cyclopropene (non-aro due to sp3) cyclopropene with a lone pair ( anti-aro) cyclopropene with positive charge (non-aro)
