PPT-2 Transition metal-free catalytic hydrogenation of ketones

Author : calandra-battersby | Published Date : 2017-05-04

Katherine Jolley and Martin Wills Department of Chemistry The University of Warwick Coventry CV4 7AL UK Introduction Results and Discussion Conclusions and proposed

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2 Transition metal-free catalytic hydrogenation of ketones: Transcript


Katherine Jolley and Martin Wills Department of Chemistry The University of Warwick Coventry CV4 7AL UK Introduction Results and Discussion Conclusions and proposed reaction mechanism Hydrogenation is . 6 286 Relative Stability of Alkenes Based On Molar Heats of Hydrogenation H hyd 276 kcalmol H hyd 286 kcalmol Trans cis brPage 3br Relative Stability of Alkenes Based On Molar Heats of Hydrogenation 327 kcalmol 297 kcalmol 280 kcalmol 286 kcalmol 18-4. Alkylation of enolates can be difficult to control.. The alkylation of an aldehyde or ketone enolate is an example of a nucleophilic substitution reaction.. The alkylation of aldehydes and ketones is complicated by several unwanted side reactions.. The Civet Cat is the original source of . civetone. , a sweet and pungent ketone used as a fixative in perfumery. Aldehydes and ketones are found in many fragrant odors of many fruits, fine perfumes, hormones etc. some examples are listed below.. E2C 2013, Budapest. Y. Jiang, R. . Kunjanpillai. , S. . Chakraborty. , . F. . Zhou. O. . Blacque. , T. Fox and H. . Berke. . Strategies . for Homogeneous . Carbon Dioxide Hydrogenations. Search . for. choline. . Receptors.. 3. . Therapeutic use in: smoking cessation and . neurodegenerational. diseases. .. Asymmetric Synthesis of the . Lupin. Alkaloids:. (-)-Cytisine, (-)-Sparteine, (+)-Anagyrine, and (+)-. 12-1. Because the C-C .  bond is relatively weak, alkene chemistry is dominated by its reactions.. The addition of a reagent, A-B, to give a saturated compound is the most common transformation of an alkene.. and . poisons. Rates of Reaction. Catalytic Converters. Exhaust fumes contain. CO – . due . to incomplete combustion of hydrocarbons. NO & NO. 2. – . N. 2. . in air is oxidised at high temperatures. Chemistry 335 Supplemental Slides: Interlude 1. 1. 1. Definition of Oxidation and Reduction. For practical purposes in organic chemistry, oxidation and reduction are defined as follows:. Oxidation:. . Triacylglycerols. Many soft margarines, stick margarines, and solid shortenings are produced by the partial hydrogenation of vegetable oils.. Learning . Goal . Draw . the condensed or line-angle structural formula for the products of a triacylglycerol that undergoes hydrogenation, hydrolysis, or saponification.. Why is:. Mn. 2 . (. aq. ) colorless. Cu. 2 . (. aq. ) less deeply blue colored than Cu(NH. 3. ). 4. 2 . Zn. 2 . (. aq. ) colorless. MnO. 4. -. deeply colored. W(CO). 6. colorless. Sigma Interaction Strength. . Purpose of this course – understanding the diagram below:. Fujimor. i. , Electronic structure of metallic oxides: band-gap closure and valence control, . J. . . Phys. Chem. . Solids . 53. (1992) 1595–1602.. Carbonyl Compounds. Contain the carbonyl group . C=O. . Aldehydes: . R may be hydrogen, usually a carbon containing group. Ketones: . R contains carbon. Short. forms. Structures of Aldehydes . and Ketones. Shatha. I . Alaqeel. 108 . Chem. Learning Objectives. Chapter eight . discusses. . carbonyl . compounds. and . by the end of this chapter the students will:. Know the structural differences between aldehydes and ketones. Dr. Satyanarayan Dhal. Lecture-24. Why Graphene ?. Discovery : 2004, . Geim. and . Nosovelov. at Manchester University. Extraordinary electronic, chemical, mechanical, thermal and optical properties. .

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