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Topic 10: Organic Chemistry P1: …….. / 15p. P2: ……. / 29p.
Topic 10: Organic Chemistry P1: …….. / 15p. P2: ……. / 29p.

... The correct IUPAC name of the molecule is 2-methylpentane. All the bond angles will be approximately 90°. One isomer of this molecule is pentane. The boiling point of this compound would be higher than that of pentane. ...
PPA 1. Testing for Unsaturation
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...  A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine  The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
Aldehydes and Ketones
Aldehydes and Ketones

...  A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine  The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
Synthesis Explorer
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... the three-membered ring of epoxyethane which is then hydrolysed with water or dilute acid to form ethane-1,2-diol. ...
Unit-2-Hydrocarbons
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Aldehydes and Ketones
Aldehydes and Ketones

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5 Alkenes and Alkynes GOB Structures
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Chapter 19 - people.vcu.edu
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... nitrogen, changing them from R to S.  There are two times when chirality is locked.  Quaternary ammonium salts  Sometimes sterics can prevent the lone pair from flipping. Physical properties o Strongly polar o Can hydrogen-bond if they are 1° or 2°  Remember that the hydrogen bonding of nitrogen ...
6.5. alcohols
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Unit 5 - Organic Chemistry 2 student notes
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Reductions of Carboxylic Acid Derivatives - IDC
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... for the reduction of aldehydes and ketones to 1º and 2º-alcohols respectively has been noted. Of these, lithium aluminum hydride, often abbreviated LAH, is the most useful for reducing carboxylic acid derivatives. Thanks to its high reactivity, LAH easily reduces all classes of carboxylic acid deriv ...
679KB - NZQA
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Working with Hazardous Chemicals

... N,4,4-Trimethyl-2-oxazolinium iodide is prepared by adding 49.5 g. (0.500 mole) of 4,4-dimethyl-2oxazoline to an excess of cold methyl iodide (182 g., 78.2 ml., 1.28 moles) in a 500-ml. flask and stirring at room temperature under argon for 20 hours. The light brown solid is suction filtered and dis ...
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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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