Explore the properties and structures of alkenes through detailed slides and images, including the general formulas of alkanes, alkenes, and alkynes. Discover the physical properties of selected alkenes such as ethene, propene, and 1-butene. Delve into the vibrant world of organic chemistry with eng

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Functional groups in organic chemistry are specific groups of atoms within molecules that determine the chemical properties of the compound. This content provides visual representations and descriptions of various functional groups such as alkanes, alkenes, alcohols, aldehydes, acids, and esters. Le

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Alkenes and alkynes are unsaturated compounds with carbon-carbon double and triple bonds, respectively. Dienes contain two double bonds that can be cumulated, conjugated, or nonconjugated. Learn about their nomenclature and classification in this informative guide.

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Alkenes are unsaturated hydrocarbons containing a C=C double bond. This chapter covers topics such as alkene structure, hybridization, naming, isomerization, physical properties, preparation methods, stability rules, and addition reactions. Learn about the sp2 hybridization of orbitals in alkenes, o

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Explore the world of polymers by learning about monomers and polymers, how alkenes are used to create polymers, and the process of polymerisation. Dive into the structure of poly(ethene) and poly(propene) through diagrams and hands-on activities with molymod kits.

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Seminar conducted by Jian Cao from Jieping Zhu's Lab at EPFL on the topic of Palladium-Catalyzed Arylhalogenation of Alkenes, covering Pd(II)/Pd(IV) and Pd(0)/Pd(II) catalytic cycles, stereochemical studies, historical development, and comprehensive research findings.

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Understanding the factors influencing SN2 reactions in synthetic gateways involving elimination reactions of alkenes is crucial for predicting reaction rates. This includes analyzing the impact of solvent types on reaction rates in different scenarios. Polar protic solvents and polar aprotic solvent

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Transition metal catalyzed trifluoromethylation is a valuable method for introducing trifluoromethyl groups into unactivated alkenes, with significant impact in pharmaceutical, agrochemistry, and material science. The incorporation of CF3 is essential due to its enhancement of metabolic stability, p

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Explore the properties and reactions of decane, catalysts, isomers, and addition reactions of alkenes in this comprehensive guide. Learn about saturated and unsaturated hydrocarbons and witness the transformation from alkenes to alkanes through different chemical processes.

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Delve into the intricacies of mass spectrometry as applied to pharmaceutical analysis, exploring the fragmentation processes, allylic cleavage in alkenes and alkynes, and the characterization of aromatic hydrocarbons. Discover how mass spectrometry aids in identifying and analyzing various compounds

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Alkenes are hydrocarbons with a double carbon-carbon bond, reacting uniquely due to their functional group. Alcohols and carboxylic acids also have distinctive properties and reactions, important in organic chemistry studies. Learn about their structures, formulas, reactions with other compounds, an

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Alkenes and alkynes are crucial types of unsaturated hydrocarbons with distinct characteristics. This content delves into their IUPAC nomenclature rules, preparation methods, qualitative tests, and reactions. It also explores naming conventions for alkenes and alkenyl groups, providing a comprehensi

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The excerpt provides detailed insights into reactions of alkenes, emphasizing main reaction classes, key characteristics, intermediate states, and specific mechanisms like bridgehead halohydrin. It covers important concepts such as carbocation addition, free radical addition, and organometallic/redo

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Detailed exploration of transition metal catalyzed olefin polymerization via coordination-insertion mechanism, including the use of Ziegler-Natta catalysts, MAO activators, and stereochemical control of poly-1-alkenes. The mechanism, catalyst types, activators, and stereochemistry effects are discus

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