ethylene‚ because of the high reactivity of its double bond‚ is readily transformed into many useful products * First member of homologous series of straight chain alkenes (C2H4) * Functional group = highly reactive double C=C bond * Readily transformed into many useful compounds ( polyethylene) through addition reactions * Examples: ethylene oxide (CH2)2O -> sterilizer Ethanol (C3COOH) -> solvent Polyethylene (CH2)n -> plastic
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Lesson 08.01: Half-life and Radioactive Decay · Distinguish between nuclear and chemical reactions. · Compare and contrast different types of nuclear decay and the properties of the three types of radiation (alpha‚ beta‚ and gamma) discussed in the lesson. · Be able to predict the isotope or radiation produced by a nuclear decay reaction when the other product is given. · Describe and make predictions regarding half-life‚ including using a graph or set of data to determine the half-life of
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Clays are one of the important natural materials‚ which have been examined for catalytic applications. Clays are characterized by a layered structure and hence they are slippery when wet. They are broadly classified as cationic or smectite type (having layer lattice structure in which two-dimensional oxyanions are separated by layers of hydrated cations) and anionic or brucite type (in which the charge on the layer and the gallery ion is reversed complimentary to smectite type). Anionic clays are
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using line-angle structural formulas. (Ex. The five constitutional isomers of C6H14) -Cycloalkanes are alkanes that contain a ring of three or more carbons -General Formula of Cycloalkane: CnH2n‚ n = number of carbon atoms Alkenes and Cycloalkenes -An alkene is an acyclic unsaturated hydrocarbon that contains one or more carbon –
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eliminated the reaction yields an alkene in which the un-protonated alcohol serves as the reaction solvent. This experiment then called for the distillation of this mixture‚ using a distillation apparatus. As this distillation took place the products‚ alkenes and water continuously distilled from the reaction mixture into a Hickman still as they were formed. The removal of these elements shifted the equilibrium to the right‚ ultimately increasing the yield of alkene‚ this is also known as Le Chatelier’s
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fractions from the refining of petroleum Catalytic cracking is the process whereby high molecular weight fractions are broken down to low molecular weight ones. This process is used in petroleum refineries where crude oil is broken down to smaller alkenes and alkanes‚ until ethene‚ propene‚ (or both) are formed. Catalytic Cracking allows greater output of high-demand products. Identify that ethylene‚ because of the high reactivity of its double bond‚ is readily transformed into many useful products
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early atmosphere - earth roughly 4 billion yrs old - created by volcanoes erupting + releasing gases - contained mostly co2 + water vapour - earth cooled + water vapour condensed to form oceans - co2 dissolved into oceans + used to form marine organism shells which were compacted to form sedimentary rock - plants evolved to photosynthesise‚ takingin co2 + releasing oxygen - scientists don’t kno where all nitrogen came from bc they weren’t there to record evidence but most theories suggest
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bonds‚ and are said to be saturated; alkenes (e.g. ethene and propene) and alkynes (e.g. ethyne) have carbon-carbon double or triple bonds‚ and are said to be unsaturated. Aromatic hydrocarbons are cyclic compounds whose structure is related to that of benzene‚ with six-electrons in a six-membered ring. For this experiment‚ hexane will be used as an example of saturated hydrocarbons (alkanes)‚ cyclohexene will be used as an unsaturated hydrocarbon (alkenes) and toluene as an aromatic hydrocarbon
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located around 1900 cm-1 indicates the presence of a benzene ring. For the product‚ the peaks located just over 3000 cm-1 indicate carbon hydrogen bonds. The weak carbon-carbon double bond peak located at 1621 cm-1 indicates the presence of a trans alkene. This is also supported by the peak located at 964.93 cm-1‚ the trans isomer peak. The two peaks at 1621.31 and 1516.29 cm-1 along with the overtones located around 1900 cm-1 indicates the presence of a benzene ring. Based on this data‚ it can be
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using the resulting aldehyde‚ along with 2‚4-dimethylpyrole‚ a BODIPY dye was obtained [36]. To facilitate intersystem crossing‚ the 2- and 6- positions of the boradiazaindacene ring system were iodinated with an iodic acid-iodine mixture [37]. Bromination at the same positions was performed via N-bromosuccinamide (NBS) [38]. 8-Palmitoyl-1‚ 3‚ 5‚ 7-tetramethyl-2‚ 6 diiodo-4-bora‚ 3a‚ 4a-diaza-s-indacene was obtained by the iodination of 8-palmitoyl-1‚ 3‚ 5‚
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