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Chromatography Spectroscopy HW
Chromatography Spectroscopy HW

... In the final stage of this process, the salicylate ion is acidified to give salicylic acid. Assuming an overall yield by mass of 45% for this three stage process, calculate the mass of phenol that is needed to produce the annual UK output of 3500 tonnes of salicylic acid. Mr of phenol = 94.0; 1 tonn ...
Arenes HW
Arenes HW

... In the final stage of this process, the salicylate ion is acidified to give salicylic acid. Assuming an overall yield by mass of 45% for this three stage process, calculate the mass of phenol that is needed to produce the annual UK output of 3500 tonnes of salicylic acid. Mr of phenol = 94.0; 1 tonn ...
Organic reactions and mechanisms
Organic reactions and mechanisms

... group upon reaction with aqueous alkalies but the Br in phenyl bromide (C6H5Br) could not be exchanged for OH under similar conditions. Therefore it was proved that the structural theory of organic reactions was made inadequate to offer satisfactory interpretation of the course of ...
chapt13
chapt13

... From a reaction perspective nucleophilic species carry a negative charge and are usually polar in character. They may have an electron rich bond or unbonded electron pair which is often the site of attack. In the environment the majority of the nucleophiles that react with organics are inorganic Tab ...
p. 634 - 643
p. 634 - 643

... halogenation (addition of halogen atoms). Ethylene and substituted ethylene molecules can undergo polymerization, a process by which many molecules (monomers) are joined together to form a large chain-like molecule. ...
Ethers, Sulfides, Epoxides - City University of New York
Ethers, Sulfides, Epoxides - City University of New York

... We are breaking the CN bond; bond order goes from 3 to 0. Probably stepwise. Chemically speaking: the nitrogen of the nitrile is basic (lone pair) and can be protonated. This makes it a better electrophile (cf. carbonyl). Multiple bond can undergo addition (cf. carbonyl) reducing bond order. Goal: B ...
Chapter 14 - people.vcu.edu
Chapter 14 - people.vcu.edu

...  See Chapter 11 Notes for mechanism Autoxidation of ethers o Once ethers are exposed to oxygen, they can begin to slowly turn into peroxides. o Peroxides are contact explosives, so if crystals get under the cap of a jar, when you open the jar, it explodes. o You don’t need to know more than that. ...


... Johnson Matthey have published an informative 82-page brochure, “The Catalyst Technical Handbook”, which covers the use of catalysts for chemical reactions important in industrial synthesis. The handbook recommends platinum group metal homogeneous, heterogeneous and FibreCatm anchored homogeneous ca ...
Aldehydes and Ketones
Aldehydes and Ketones

... We are breaking the CN bond; bond order goes from 3 to 0. Probably stepwise. Chemically speaking: the nitrogen of the nitrile is basic (lone pair) and can be protonated. This makes it a better electrophile (cf. carbonyl). Multiple bond can undergo addition (cf. carbonyl) reducing bond order. Goal: B ...
A2 Chemistry
A2 Chemistry

... An nucleophile is an A zwitterion is a dipolar ionic A condensation reaction is one atom/s attracted to an form of an amino acid that is in which 2 small molecules electron deficient centre formed by the donation of a react together to form a larger where it donates a pair H+ ion from the carboxyl ...
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... Nomenclature of aromatic hydrocarbons ...
Chapter 17 Allylic and Benzylic Reactivity
Chapter 17 Allylic and Benzylic Reactivity

... anion resulting from removal of the central hydrogen is both allylic and propargylic, and is therefore doubly resonance-stabilized. The conjugate-base anion is alkylated by allyl bromide. ...
organic chemistry 307
organic chemistry 307

... a name that will unambiguously identify the compound. One name must equal one compound. Unfortunately the reverse is not true, except in a naming system. a. Systematic and Common names; discuss how we will deal with them. b. What must a name do? i. Indicate the number of C atoms ii. Indicate the car ...
Bk3BP08EE
Bk3BP08EE

... The nucleophilic ammonia attacks the partially positive carbon to which the electronegative chlorine is attached resulting in the formation of a pentavalent transition state. The C – Cl bond is being broken as the C – N bond is formed. The resultant organic product is ethylamine, CH3CH2NH2. The amin ...
Reactions of Alkenes
Reactions of Alkenes

PPT
PPT

... • An italic “N” is used to indicate that an alkyl group is attached to the nitrogen and not to the ring. Examples: ...
synthesis in industry
synthesis in industry

... tallic compound as a reagent, but both cases require a second metal compound as a catalyst to promote C -C bond formation. SELECTIVE ALKYLATION OF NAPHTHOQUINONES A wide ...
Print this page
Print this page

... Functional groups you should know These are important in both artificial polymers and in biochemistry, not to mention organic chemistry in general. Alcohol: An oxygen atom singly-bound to one hydrogen atom and one carbon atom. ...
Conversion of Alcohols into Alkyl Halides
Conversion of Alcohols into Alkyl Halides

... 3 alcohol ...
HL  ISSN: 2231 – 3087(print) / 2230 – 9632 (Online)
HL ISSN: 2231 – 3087(print) / 2230 – 9632 (Online)

... room temperature. The Mannich base was then acetylated by refluxing it with acetic anhydride for about 24 hrs and the volatile material was distilled out under reduced pressure to give crude diacetate. It is not purified further and directly treated with conc. Hydrochloric acid to gives 2hydroxy-5-f ...
Organic Chemistry
Organic Chemistry

... that is attached to two other carbon atoms - named by replacing the final –e from the corresponding alkane with –one; if necessary, cite which carbon atom the carbonyl group is attached to. ...
Chemistry 235, Winter 2008  Name: General rules:
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... • In compounds, the more electronegative element (p. 137) is assigned the negative oxidation number. • Hydrogen in an organic compound is assigned an oxidation number of +1. • Oxygen in an organic compound generally is assigned an oxidation number of –2. • The sum of all of the oxidation numbers of ...
Topic 17 specification content - A
Topic 17 specification content - A

... I can describe the nucleophilic addition–elimination reactions of water, alcohols, ammonia and primary amines with acyl chlorides and acid anhydrides and outline the mechanism of the nucleophilic addition–elimination reactions of acyl chlorides with water, alcohols, ammonia and primary amines ...
EXPERIMENT 5: Oxidation of Alcohols: Solid
EXPERIMENT 5: Oxidation of Alcohols: Solid

... relationship has led to the development of a convenient qualitative test for distinguishing primary and secondary alcohols (and aldehydes) from tertiary alcohols (and ketones). The qualitative test involves the addition of a solution of CrO3 in sulfuric acid (Jones' Reagent) to a solution of the com ...
H + - uaschemistry
H + - uaschemistry

... • For physical evidence, include a comparison of carbon– carbon bond lengths in alkanes, alkenes and benzene, and the number of structural isomers with the formula C6H4X2. • For chemical evidence, include a comparison of the enthalpies of hydrogenation of benzene, cyclohexene, 1,3-cyclohexadiene and ...
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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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