This preview shows pages 1–2. Sign up to view the full content.
This preview has intentionally blurred sections. Sign up to view the full version.View Full Document
Unformatted text preview: 1,3-Butadiene (16.1) Planar due to significant double bond character between C2 and C3 This is due to -electron delocalization 2 Conjugated vs. Isolated Dienes (16.1) Allylic Carbocations (16.1; 16.2) Stabilized by resonance Electron Delocalization, Hybridization and Geometry (16.5) In any system X=Y-Z: , Z is sp 2 hybridized and the nonbonded electron pair occupies a p orbital to make the system conjugated...
View Full Document
This note was uploaded on 10/24/2011 for the course CHEMISTRY 623 taught by Professor Benson during the Spring '11 term at Kansas.
- Spring '11
- Organic chemistry