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Regents Unit 15: Hydrocarbon Derivatives
Regents Unit 15: Hydrocarbon Derivatives

CARBONYL COMPOUNDS
CARBONYL COMPOUNDS

... It is a disproportionation reaction that takes place on aldehydes with no H atoms on the αcarbon. E.g. methanal is in the presence of NaOH simultaneously oxidised to ………………….. and reduced to……………………. 2 HCHO  2 C6H5CHO  3. Reactions on the α -carbon a. halogenation  α - halogenocompounds CH3COCH3 ...
doc CHEM 222 Lab exam with Answers
doc CHEM 222 Lab exam with Answers

... is obtained via insertion into the double bond. 5.__T___ Carbenes are very reactive towards nucleophiles because of an empty orbital on the carbene carbon. 6.__F___ An emulsion is essential in the Carbene lab in order to increase the temperature and thus maximize the yield. 7.__ T__Biphenyl is solub ...
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Chapter 14 Selenium reagents

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thiols and sulfides.
thiols and sulfides.

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Quiz 3 – Aldehydes and Ketones 1 Which of the following reactions

... 7 You have two C6H10O ketones, I and II. Both are optically active, but I is racemized by treatment with base and II is not. Wolff-Kishner reduction of both ketones gives the same achiral hydrocarbon, formula C6H12. What reasonable structures may be assigned to I and II? A) I is 3-methyl-4-penten-2- ...
幻灯片 1
幻灯片 1

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Total marks available
Total marks available

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Exam 1
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- SlideBoom
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... 40 mL of saturated sodium bicarbonate solution to the organic layer remaining in the funnel. Gently swirl the funnel several times until the bubbling ceases. Then, stopper the funnel, invert it, and vent immediately. Shake the funnel and vent it at regular intervals. Place the funnel back in the rin ...
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Rxns of Alkynes

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Acid Basics
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... Acids are compounds that give up hydrogen nuclei. What is a hydrogen nuclei? It’s a proton. So acids give up protons. Recall that 99.9 % of all hydrogen (H) has no neutrons in the nucleus and it’s just a proton. Here’s an example: HCl (hydrochloric acid, the acid in your stomach that breaks down foo ...
CHM412 June 2013 paper
CHM412 June 2013 paper

... efficient test is the Lucas test. A solution of ZnCl2 in c.HCl has a small amount (say ½ cm3) of the unknown alcohol added to it. If the solution goes ‘cloudy’ (sometimes called ‘turbid’) almiost immediately, then the alcohol was a 3 o alcohol. If after about 30 seconds it goes cloudy then it was a ...
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Haloalkane



The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.
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