Neha jain presentation on reac. intermedites 14 03-2013

of 26 /26
REACTION INTERMEDIATES: CARBENE, NITRENE & ARENE/BENZYNE By: Neha Jain Ms. Neha Jain (M.Sc., M.Phil, Research Scholar) Laboratory of Endocrinology, Department of Biosciences, Barkatullah University, Bhopal-462026, M.P., India

Embed Size (px)

Transcript of Neha jain presentation on reac. intermedites 14 03-2013

  • 1.By:Neha Jain Ms. Neha Jain(M.Sc., M.Phil, Research Scholar)Laboratory of Endocrinology, Department of Biosciences,Barkatullah University, Bhopal-462026, M.P., India

2. 1. If a reaction occurs in more than one step, it must involve species that are neither the reactant nor the final product.2. These are called reaction intermediates or simply intermediates3. Each step has its own free energy of activation.4. Reactive intermediates are usually short lived and are very seldom isolated.5. The complete diagram for the reaction shows the free energy changes associated with an intermediate. 2 3. For example, consider this hypothetical stepwise reaction:A+B C+DThe reaction includes these elementary steps:A + B X*X* C + DThe chemical species X* is an intermediate. 4. CARBOCATION CARBANION FREE RADICLE CARBENE NITRENE ARENE/BENZYNE 5. 5 6. 6 7. This is the species with central carbon atom with two bonds and twoelectrons.These are uncharged species and 6 valence electrons.These electrons are may be paired or unpaired.These are very short lived species.The smallest and simplest species of this class is methylene, this isnon isolable species.When the electrons are paired the Carbene has singlet state and incase of unpaired electrons the Carbene has triplet state.These are extremely reactive species and can beAs these species are short lived and very reactive hence it is difficultto detect. 8. 1. Nitrene is electro-neutral monovalent electron species.2. This has similar properties as that of carbene. Hence Nitrene is called as nitrogen analogue of carbene.3. There are six electrons present on nitrogen in Nitrene.4. Carbenes are less stable than Nitrene.5. Generation of Nitrene is possible in both triplet and singlet state but mostly the ground state for Nitrene is triplet. 9. 1. It is non isolable very reactive species with the hexagonal planar rind structure with 6 pi delocalizing and 2 additional pi electrons.2. The addition two pi electrons do not affect the aromatic character of ring as it does not interfere with the Huckel number.3. This is a six membered ring containing C-C triple bond this triple bond gives high reactivity to the species. 10. A Kulkarni and Kalyani. D. Asgaonkar Study ofVarious Reaction Intermediates Juilee., P 325 -351,Vol. 3 (1) Jan Mar 2012 www.ijrpbsonline.comSachin Kumar Ghosh, General organic chemistry, A modern approach, fundamentals of organic reaction mechanism, new Alipore college New central book agency, May 1994, 11. Thanks !!!