5 Nov woodward fieser rule. 1. Presented by: cy 1st yr Department of pharmaceutical analysis; 2. Introduction. WOODWARD-. 5 May Brief description of Woodward Fieser Rules. * Examples for all te 3 rules. Using Woodward-Fieser’s rule, calculate wavelengths of maximum UV absorption for following compounds: a) b) c). Base value: nm. Base value: nm.
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The Woodward rules are specifically related to the effect of groups in conjugationa simple test of which is to see if you can push curly arrows between the pi bonds. If you find a double bond outside a ring as in the 4 ring system hereit will be considered as exocyclic.
With the aid of these rules the UV absorption maximum can be predicted, for example in these two compounds: Central Connecticut State University. Exocyclic is defined as being outside of the ring system or in more complex systems, outside of the ring system fiesre consideredthe bond highlighted is indeed inside the ring system and is as such endocyclic.
Woodward’s rules are an empirical method for predicting the maximum absorption of a molecule based on the functional groups present that is, conjugated functional groups which possess a distinctive maximum absorbance such as a diene or an unsaturated carbonyl.
Khurram Javed 1 1. Thanks for the answer. For example, in this compound, should the marked double bond considered as an exocyclic double bond? So, the pointed double bond is exocyclic to rupe adjoining cyclopentane ring.
Woodward’s rules – Wikipedia
Retrieved from ” https: Views Read Edit View history. Alkyl substituent or ring residue. One set of Woodward—Fieser rules for dienes is outlined in table 1.
Fieser; Mary Fieser; Srinivasa Rajagopalan Archived from the original on April 10, Woodward Fieser rules for dienes – non conjugated double bond as exocyclic? Pritt Balagopal 5, 2 14 From Wikipedia, the free encyclopedia.
If we start with the alkene at the bottom left, then it is in conjugation with an endocyclic alkene to the immediate right and an exocyclic alkene in the ring to the right hand side. Rules for wavelength of maximum diene absorption   With the aid of these rules the UV absorption maximum can be predicted, for example in these two compounds: For polyenes having more than 4 conjugated double bonds one must use Fieser—Kuhn rules.
Post as a guest Name. This page was last edited on 1 Juneat Inputs used in the calculation are the type of chromophores present, the substituents on the chromophores, and shifts due to the solvent.
Sign up using Email and Password. VirtualText of Organic Chemistry. These double bonds are all in conjugation with one another.
Physical organic chemistry Spectroscopy.
Questions Tags Users Badges Unanswered. But according to the paper by Fieser the pointed double bond is exocyclic to the 5 membered ring or right.
Sign up using Facebook. Should the marked double bond considered as an exocyclic double bond? A diene is either homoannular with both double bonds contained in one ring or heteroannular with two double bonds distributed between two rings.