Title of Experiment: An Activity Series Lab MSDS: Copper‚ Cu(s) Stability- Stable. Incompatible with strong acids‚ active halogen compounds‚ chlorine‚ fluorine‚ iodine‚ bromine‚ ammonia. May react explosively with strong oxidizing agents. Toxicology-Dust may cause respiratory irritation. Personal Protection- Suitable ventilation if handling powder. Zinc‚ Zn(s) Stability-Stable. Incompatible with amines‚ cadmium‚ sulfur‚ chlorinated solvents‚ strong acids‚ strong bases. Air and moisture
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"CHEMISTRY REVIEW" PROJECT PAGES This Project Page first appeared in the November 1996 issue of Chemistry Review‚ Volume 6‚ Number 2‚ Pages 14 and 15. Chemistry Review is published four times during the academic year by Philip Allan Updates and is a journal for post-16 students. It contains a variety of interesting and colourful articles aimed at 16-19 year-olds taking mainly AS and A2 courses in chemistry. NOTE: Project Page is designed to help you think about your investigation. It is not
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Lewis base. It can therefore be saturated by the addition of a halogen to the double bond. Both of the reactants are non-polar but there is an induced polarity during the reaction due to the electron-rich site at the double bond‚ which results in bromine acting as an electrophile. In this reaction‚ the cinnamic acid reacts as an alkene. Alkenes are unsaturated hydrocarbons with a carbon-carbon double bond. In a double bond‚ a pair of electrons lies between the carbon atoms in a σ bond and the other
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Question 1 0 out of 2 points When electricity is passed through molten potassium bromide‚ two simpler substances‚ potassium and bromine‚ are produced. Therefore‚ potassium bromide Selected Answer: has less mass than the resulting potassium and bromine do. Correct Answer: cannot be an element. Question 2 2 out of 2 points Which of the following parts (postulates) of Dalton’s atomic theory has been modified in light of later discoveries? Selected
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Write your name here Surname Other names Centre Number Candidate Number Edexcel IGCSE Chemistry Unit: 4CH0 Science (Double Award) 4SC0 Paper: 1C Wednesday 25 May 2011 – Morning Time: 2 hours Paper Reference 4CH0/1C 4SC0/1C You must have: Ruler Candidates may use a calculator. Total Marks Instructions black ink or • Usein the boxesball-point pen. page with your name‚ Fill at the top of this • centre number and candidate number. all • Answer
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Stoichiometry Practice Problems Be sure to balance all equations before you start calculating! Answer key is at the end. 1) Lithium hydroxide reacts with hydrobromic acid to produce lithium bromide and water. If you start with ten grams of lithium hydroxide‚ how many grams of lithium bromide will be produced? 2) Ethylene (C2H4 ) reacts with oxygen gas to produce carbon dioxide and water. If you start with 45 grams of ethylene‚ how many grams of carbon dioxide will be produced?
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N-dimethylformamide)‚ a classic solvent for SN2 reactions. With all the conditions in favor of this reaction‚ it should be no surprise that this reaction works very well Despite the ease of our reaction‚ a few comments are in order. Our alkyl halide‚ cinnamyl bromide‚ is extremely reactive. As an electrophile‚ it is activated by something called the phenacyl effect (Reeve J. Am. Chem. Soc. 1954‚ 76‚ 2280-2281). The phenacyl effect applies to halides that are adjacent to a _-bond‚ such as a simple double bond‚
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terephthalic acid is produced by oxidation of p-xylene by oxygen in air: Diagram 3.1 The process uses cobalt-manganese-bromide catalyst. The bromide source can be NaBr‚ HBr or tetrabromoethane where bromine functions as a regenerative source of free radicals. In this process‚ acetic acid is the solvent and oxygen from compressed air is the oxidant. The combination of bromine and acetic acid is found to be highly corrosive and hence the equipment is lined with titanium.
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Acetylene gas was used for the selective reactivity of hydrocarbons to functional group tests; Bayer’s test‚ Bromine test light‚ Bromine test dark‚ and Tollen’s test. In Bayer’s test‚ only Acetylene‚ Eugenol and Unknown hydrocarbon 2 reacted positively and the rest retain the purplish color of KMnO4. On the other hand‚ the five compounds in Bromine test with light reacted positively. In Bromine test dark‚ Hexane and Unknown hydrocarbon 1 did not react because light (UV) is absent. Lastly‚ in Tollen’s
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Preparation of 4-bromoaniline Introduction Aromatic compounds tend to undergo electrophilic aromatic substitutions rather than addition reactions. Substitution of a new group for a hydrogen atom takes place via a resonance-stabilized carbocation. As the benzene ring is quite electron-rich‚ it almost always behaves as a nucleophile in a reaction which means the substitution on benzene occurs by the addition of an electrophile. Substituted benzenes tend to react at predictable positions. Alkyl groups
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