PPT-Reactivity of Polycyclic Benzenoid Hydrocarbons

Author : tawny-fly | Published Date : 2016-12-01

166 Naphthalene is activated toward electrophilic substitution Naphthalene undergoes electrophilic substitution rather than addition Naphthalene is activated with

Presentation Embed Code

Download Presentation

Download Presentation The PPT/PDF document "Reactivity of Polycyclic Benzenoid Hydro..." is the property of its rightful owner. Permission is granted to download and print the materials on this website for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.

Reactivity of Polycyclic Benzenoid Hydrocarbons: Transcript


166 Naphthalene is activated toward electrophilic substitution Naphthalene undergoes electrophilic substitution rather than addition Naphthalene is activated with respect to electrophilic aromatic substitution Bromination at C1 occurs without a catalyst under mild conditions. Alkanes, alkenes, alkynes and aromatics. Types of Hydrocarbons. Hydrocarbons contain C and H. There are 4 families, alk. anes. only have C-C single bonds, alk. enes. have at least one C=C and alk. ynes. By Kathleen Barbosa. Forensic Chemistry. Arson Investigations. Components of ignition and combustion reaction . Fuel. Oxidizing Agent. Heat. Uninhibited Chemical Chain Reaction. Identify. . Ignitable. , and polycyclic aromatic hydrocarbons (PAHs) are substances that are on the Biological Nutrients Banned List but not the Technical Nutrients Banned List. While these substances can be used in some ma Finding the . Clar. number and the Fries number of a . benzenoid. in polynomial time using a LP.. The desired solutions are integer but it has been proven that the basic feasible solutions are all integral so integer programming tactics are not required.. Orbitals. Natural gas?. Fig. 11.1. Aliphatic Hydrocarbon Structure Comparison. Bonding and Geometry. of Two-Carbon Molecules . 11.1 Structure and Physical. . Properties. Finding a measurable amount of one or more PAH metabolites in the urine does not mean that the levels of one or more PAH metabolites or PAHs cause an adverse health effectBiomonitoring studies on leve Daniele Fabio Zullino. 1. , Emmanuelle Fr. é. sard. 2. , Riaz Khan. 1. , Djamel Benguettat. 1. , Fabian Clays. 2. , Yves Montagrin. 2. , Farfalla Ribordy. 2. , Sophie Taparel. 2. , Sonia Krenz. Baseline . (Flightpath D):. List the order of common metals in the reactivity series. Use general equations to write specific word equations for metals listed in the reactivity series reacting with oxygen, water, and acid. Safely make and record observations.. 22.1 Hydrocarbons. Organic Chemistry. includes almost all carbon compounds. Not limited to compounds found in living cells. Hydrocarbon: organic compound made of only hydrogen and carbon atoms. hydrocarbons. 1. Nomenclature . of Polycyclic Aromatic Compounds. Polycyclic . aromatic compounds have two or more benzene rings fused together. 2. Naphthalene, anthracene and phenanthrene are obtained from . coal tar. “Dr. Dave” Janzen, D. Min., CISM, CAI. Certified Intervention Professional #I0175. “The Motiventionist”. http://www.motiventionist.com. /. Rev. . 9-14-2015. Objectives. Define . Emotional . Reactivity. MICHAEL FARADAY (1791-1867). first person to isolate and identify benzene. early benzene uses:. - . decaffeinate . coffee. - antiknock additive . in gasoline. - solvent in chem rxns. now we know benzene is a carcinogen!. Nora . Zannoni. Valerie Gros, Roland Sarda-Esteve,. Sebastien Dusanter, Vincent Michoud, Vinayak Sinha. OH . reactivity. : . meaning. and . importance. CH. 4. ?. Sources. Sinks. ∙OH. Ozone. SOA. OH budget. Bold entries indicate new or changed listings in the Fifteenth Report on Carcinogens. Known To Be Human Carcinogens Aatoxins Alcoholic Beverage Consumption 4-Aminobiphenyl Aristolochic Acids Ars

Download Document

Here is the link to download the presentation.
"Reactivity of Polycyclic Benzenoid Hydrocarbons"The content belongs to its owner. You may download and print it for personal use, without modification, and keep all copyright notices. By downloading, you agree to these terms.

Related Documents