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PPT - Gmu
PPT - Gmu

... Electrophilic Substitution Directing Effects on Aromatic Ring Effects of Activating (Electron Donating) Groups on the Orientation of Substituted Electrophiles The Amino group is a strong activating group. Even though the amino group is more Electronegative than the attached Carbon the electron rele ...
Reactions of Alkenes: Addition Reactions
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Alcohols and phenols - Home - KSU Faculty Member websites
Alcohols and phenols - Home - KSU Faculty Member websites

... Physical Properties of Alcohols 1) Solubility Of Alcohols and Phenols  Alcohol and water contain hydroxyl group that can form hydrogen bonds.  The hydroxyl group is hydrophilic “water loving”  The alkyl group of alcohols is hydrophobic “ water hating” ...
Alcohols, Diols, and Thiols
Alcohols, Diols, and Thiols

... Carboxylic acids are exceedingly difficult to reduce. Acetic acid, for example, is often used as a solvent in catalytic hydrogenations because it is inert under the reaction conditions. Lithium aluminum hydride is one of the few reducing agents capable of reducing a carboxylic acid to a primary alco ...
Organic Chemistry Fifth Edition
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Some more basic organic (more naming, reactions, polymers)
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PPT
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Chapter 16, Amines
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+ CH - Loreto Chemistry from 2015
+ CH - Loreto Chemistry from 2015

... Ammonia reacts with acyl chlorides in a similar way. However ammonia is basic so will react with the HCl formed to make a salt. We use two ammonia molecules in the equation – the first NH3 reacts with the acyl chloride to produce the amide and HCl. The second NH3 mops up the HCl produced forming the ...
advanced chem
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Links - American Chemical Society
Links - American Chemical Society

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amines - Gneet`s
amines - Gneet`s

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OXAZOLINES: THEIR SYNTHESIS AND BIOLOGICAL ACTIVITY
OXAZOLINES: THEIR SYNTHESIS AND BIOLOGICAL ACTIVITY

... From Ammonium salt Reaction of carboxylic acid 56 and 2-haloethylammonium salts 57 gives 2oxazolines 58 34. The reaction involves dehydrocondensation of carboxylic acids and 2haloethylammonium salts leading to the formation of N-(b - haloethyl) amides, which then converted into 2-oxazolines by the t ...
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QUESTION BANK CHEMISTRY-XII THE SOLID STATE CHAPTER
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... the volume of resulting solution is more than 60ml.  13. When is the value of Vant Hoff factor more than one?  14. Give an example of a compound in which hydrogen bonding results in  the formation of a dimer.  ...
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... Despite the bewildering variety of reducing agents available for synthetic tasks, new, and selectivity-en'hanced reductants are still being sought. Most popular of selective reducing agents are the various metal hydrides, mainly those of boron and aluminum, an abundance of which have been developed ...
ALDEHYDES & KETONES - Rogue Community College
ALDEHYDES & KETONES - Rogue Community College

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101. Alcohols as alkylating agents in heteroarene C H functionalization

... and trifluoromethyl groups) can be converted into the desired methylation products in high yield (26–32, 65–91% yield). Next, we sought to investigate the nature of the alcohol coupling partner, as demonstrated in Fig. 3b. A broad array of primary alcohols can effectively serve as alkylating agents ...
Chapter 17
Chapter 17

... ƒ Alkylbenzenes are oxidized to benzoic acid by heating in basic KMnO4 or heating in Na2Cr2O7/H2SO4. ƒ The benzylic carbon will be oxidized to the carboxylic acid. Chapter 17 ...
Suggested Problems for Chapter 1
Suggested Problems for Chapter 1

... Please write your name above and on the back of the last page. ...
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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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