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Conjugated Systems CHEM 4201 Fall 2014 Dr. Sheppard.

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Presentation on theme: "Conjugated Systems CHEM 4201 Fall 2014 Dr. Sheppard."— Presentation transcript:

1 Conjugated Systems CHEM 4201 Fall 2014 Dr. Sheppard

2 Conjugated systems Benzene
Commonly found in nature as pigments, hormones Isoprene

3 outline Structure Reactions MO Theory UV Spectroscopy

4 I. Structure Consider molecules with multiple double bonds…
Example: pentadienes cumulated (allenes) conjugated isolated separated by: 0 single bonds single bond or more single bonds Which is most stable? Why? Long answer = molecular orbital theory Short answer = orbital overlap

5 1,3-butadiene stability Unusually strong s bond from greater s-character of C atoms

6 1,3-butadiene stability Overlap of p atomic orbitals
In its most stable conformation, the p orbitals are parallel Allows for p electron delocalization Single bond has partial C=C character, which also contributes to stability

7 Structure, cont. Conformations of 1,3-butadiene:
s-cis (single cis) = double bonds on same side of single bond s-trans (single trans) = double bonds on opposite sides of single bond The two conformations easily interconvert at room temperature Which conformation is more stable?

8 Conformations of conjugated dienes
Mild steric hindrance in s-cis conformation

9 II. Reactions of conjugated compounds
Electrophilic addition The Diels-Alder reaction Pericyclic reactions


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