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. UV Spectroscopy. Woodward Fieser Rules for Dienes. • Woodward & Fieser derived a set of empirical rules for the estimation of wavelength for the low energy π.

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With the aid woodward fieser rule these rules the UV absorption maximum can be predicted, for example in these two compounds: Tu Nguyen September 23, at 5: Unknown April 4, at 9: The presentation is successfully added In Your Favorites. Fieser Rules If more than four double bond are present the Woodward rule is not applicable.

Fieser; Mary Fieser; Srinivasa Rajagopalan Dear First Woodward fieser rule students. Example 1 Example 2 Example 3: Dienes A diene is either homoannular with both double bonds contained in one ring or heteroannular with two double bonds distributed between woodward fieser rule rings. Please also study the tutorials for other examples. I also found some more sample problems using Woodward-Fieser rules which might help other readers.

woodwaed I hope that this tutorial will help you. Rules developed by Woodward in then expanded by Feiser in Presentation Description No description available.


Solved: UV/Vis Spectroscopy Woodward-Fieser Rules For Dien |

For polyenes having more woodward fieser rule 4 conjugated double bonds one must use Fieser—Kuhn rules. WordPress Embed Customize Embed. Rules for wavelength of maximum diene absorption [3] [7] With the aid of these rules the UV absorption maximum can be predicted, for example in these two compounds: Nur Afiza June 10, at 1: Let’s look at the questions in the previous quiz.

This page was last edited on 1 Juneat If the molecule contains both homoannular system and the heteroannular system. If the substituents woodward fieser rule not directly attached to the carbons of the system, it rieser not affect the UV-Visible absorption spectrum of the molecule. Both double bonds in the central B ring are exocyclic with respect to rings A and C.

Archived from the original on April 10, This may be differs from observed values by Not so difficult,isn’t it. woodward fieser rule

Alkyl substituent or ring residue. Miss Izalika October 2, at Heng Liang Ming June 9, at 7: Woodward fieser rule Fieser modified these rules with more experimental data, and the modified rule is known as Woodward- Feiser Rules.

Woodward’s rules

The Fieser rule must be applied for certain plants pigments such as carotenoids with even more than 4 conjugated double bonds. Go to Application Have a question?


The plant pigments contains double bond up to 11 for this Fieser rule is used. Exo stands for a double bond outside the ring and Endo stands for rrule double bond within the ring.

Physical organic chemistry Spectroscopy. V absorption rules were developed by Robert Burns Woodward I woodward fieser rule you all the best for exams and happy studying!

Good Molecules: Calculating UV λmax of molecules using the Woodward-Fieser Rules

Newer Post Older Post Home. Central Connecticut State University. From Wikipedia, the free encyclopedia. Inputs used in the calculation are the type of chromophores present, the substituents on the chromophores, and shifts due to the solvent.

Unknown February 28, at 8: Views Read Edit View history. To sum it up, follow these general steps: Ng Chai Hwai April 18, at 6: Thanks for the comment and sharing of another woodward fieser rule site on pharmacy and pharmaceutical chemistry.

Treating this conjugated system as a whole, go along the chain looking for alkyls or auxochromes woodward fieser rule attached to it, anything far from the chain not counted.