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... The selective binding of metallic ions by macrocyclic compounds is important in nature. Several antibiotics, such as nonactin, have large rings that contain regularly spaced oxygen atoms. Nonactin (which contains four tetrahydrofuran rings joined by four ester links) selectively binds K+ (in the pr ...
FYBSc Revised Syllabus
FYBSc Revised Syllabus

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CHM2210 Organic Chemistry 1
CHM2210 Organic Chemistry 1

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to get Period 2 8

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... CH3OH + NaNH2 ---> NH3 + CH3O- Na+ (sodium methoxide) most commonly made by direct reaction with active metals CH3OH + Na ---> 1/2 H2 + CH3O- Na+ (CH3)3COH + K ---> 1/2 H2 + (CH3)3CO-K+ ...
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R-c-H+H-oH:n-J-u oo o il o o o I o

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... potassium chloride, potassium iodide and potassium sulfide into 11 wells. In each reaction, the silver ion and the potassium ion changed places, so that you ended up with potassium nitrate and one of four salts - either silver bromide, sulfide, chloride or iodide. To do this, there has to be a match ...
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http://www.twitter.com/chem442bausch - SIU

... forms? (a) aldehydes; (b) carboxylic acids; (c) cis 1,2-diols; (d) trans 1,2 diols (p 629) NaBH4 and LiAlH4 are reagents often used in… (a) preparation of alcohols via oxidation of C=O bonds; (b) preparation of alcohols via reduction of C=O bonds; (c) preparation of alkanes via reduction of C=C bond ...
Organic Chemistry - Salisbury Composite High | Home
Organic Chemistry - Salisbury Composite High | Home

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... • Thioethers are compounds which contain a sulfur atom between two carbons, neither of which has a double bond to oxygen. o Thioethers are also called sulfides. o Thioethers tend to have unpleasant odors, similar to thiols. This odor has been described as the smell of oysters stored in the fridge fo ...
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... Electrostatic attraction between lone pairs (e.g., on N, O, S, F, Cl, …) and a hydrogen atom bonded to an electronegative atom (e.g., on N, O, S, F, Cl,…) - Hydrogen is δ+ because of dipole - Heteroatom has lone pair(s) of electrons H ...
Date - Chaminade University`s syllabus repository
Date - Chaminade University`s syllabus repository

... Course Objectives: This is the first part of a two-semester course in organic chemistry, where carbon compounds are studied on the basis of their functional groups. Following a review of the basic principles in general chemistry, acid-base reactions will be investigated with an emphasis on electron ...
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... – Basically hydrocarbons with a few substitutions • These substituted bonds are more reactive than C-H bonds • Therefore, when molecules with the substituted bonds react, the reaction site is generally at the substituted bonds ...
polymer - MrSimonPorter
polymer - MrSimonPorter

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Organic Chemistry I Mario Lintz 1st Year MD/PhD Candidate Mario

... o 3) remove the protecting group  Alcohol behaves as the nucleophile. (As is often the case)  OH easily transfer H to a basic reagent, a problem in some reactions.  Conversion of the OH to a removable functional group without an acidic proton protects the alcohol  One common method of alcohol pr ...
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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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