Study_guide_2010-01
... are indicated clearly by chapter and page numbers where necessary. Topics NOT from Clayden are listed in italics. PLTL topics are in CAPS. This document will be updated throughout the term. The goals of this course are: - to achieve an advanced understanding of the reactivity of organic molecules - ...
... are indicated clearly by chapter and page numbers where necessary. Topics NOT from Clayden are listed in italics. PLTL topics are in CAPS. This document will be updated throughout the term. The goals of this course are: - to achieve an advanced understanding of the reactivity of organic molecules - ...
Exam 1 - Winona State University
... III. Propose a synthetic sequence that could be used to carry out each of the following transformations in ...
... III. Propose a synthetic sequence that could be used to carry out each of the following transformations in ...
Lesson Plan
... Learning outcomes (taken from OCR A) Students should be able to: Describe addition reactions of alkenes (e.g. ethene, propene), with: o hydrogen in the presence of a suitable catalyst i.e. nickel, to form alkanes o halogens to form dihalogenoalkanes, including the use of Br 2 as a test for unsatur ...
... Learning outcomes (taken from OCR A) Students should be able to: Describe addition reactions of alkenes (e.g. ethene, propene), with: o hydrogen in the presence of a suitable catalyst i.e. nickel, to form alkanes o halogens to form dihalogenoalkanes, including the use of Br 2 as a test for unsatur ...
Παρουσίαση του PowerPoint
... Therefore, RLI, NH2-, RO-, H-, attack on the carbonyl and RMgBr, R3N, RS-, and stable carbanions tend to give the Michael type products. ...
... Therefore, RLI, NH2-, RO-, H-, attack on the carbonyl and RMgBr, R3N, RS-, and stable carbanions tend to give the Michael type products. ...
Chemistry 3.5 - CashmereChemistry
... Pour this into a pear shaped flask Carefully add 5mls of concentrated HCl Place a condenser on top of the flask and secure it in a retort stand with a water bath. Then warm the solution until a solid forms. Cool the solution to room temperature by placing the flask in a cold water bath ie a 250ml be ...
... Pour this into a pear shaped flask Carefully add 5mls of concentrated HCl Place a condenser on top of the flask and secure it in a retort stand with a water bath. Then warm the solution until a solid forms. Cool the solution to room temperature by placing the flask in a cold water bath ie a 250ml be ...
Functional groups and homologous series
... is known as SN1 (unimolecular nucleophilic substitution). The mechanism for the hydrolysis of secondary halogenoalkanes (e.g 2-bromopropane CH3CHBrCH3) is more complicated as they can proceed by either SN1 or SN2 pathways or a combination of both. ...
... is known as SN1 (unimolecular nucleophilic substitution). The mechanism for the hydrolysis of secondary halogenoalkanes (e.g 2-bromopropane CH3CHBrCH3) is more complicated as they can proceed by either SN1 or SN2 pathways or a combination of both. ...
Orbitals - drjosephryan.com
... Lithium diorganocopper reagent is prepared by reaction of 1 equivalent of copper(I) iodide and 2 equivalents of an organolithium reagent, RLi • Organolithium reagent is prepared by reaction of lithium metal with an organohalide ...
... Lithium diorganocopper reagent is prepared by reaction of 1 equivalent of copper(I) iodide and 2 equivalents of an organolithium reagent, RLi • Organolithium reagent is prepared by reaction of lithium metal with an organohalide ...
04 Carbon
... – Carbon has little tendency to form ionic bonds by loosing or gaining 4 electrons. – Instead, carbon usually completes its valence shell by sharing electrons with other atoms in four covalent bonds. – This tetravalence by carbon makes large, complex molecules possible. ...
... – Carbon has little tendency to form ionic bonds by loosing or gaining 4 electrons. – Instead, carbon usually completes its valence shell by sharing electrons with other atoms in four covalent bonds. – This tetravalence by carbon makes large, complex molecules possible. ...
Ch. 8 Carbon Chemistry
... B. Form stable compounds with halogen family C. If Hydrogen is substituted, entirely different compound is made D. A substituted hydrocarbon is when atoms of other elements replace one or more atom/s. ...
... B. Form stable compounds with halogen family C. If Hydrogen is substituted, entirely different compound is made D. A substituted hydrocarbon is when atoms of other elements replace one or more atom/s. ...
Chapter 12: Alkanes
... What are the general properties and chemical reactions of alkanes? Be able to describe the physical properties of alkanes and the products formed in the combustion and halogenation reactions of alkanes. ...
... What are the general properties and chemical reactions of alkanes? Be able to describe the physical properties of alkanes and the products formed in the combustion and halogenation reactions of alkanes. ...
Alkanes In alkanes, the C-C bonds are weaker than the C
... In alkanes, the C-C bonds are weaker than the C-H bonds. Ionisation of the molecule results in greatly reduced bond strengths. Due to the delocalised nature of the charge, all bonds are weakened equally. The mass spectra of unbranched alkanes show groups of ions separated by 14Da. This separation is ...
... In alkanes, the C-C bonds are weaker than the C-H bonds. Ionisation of the molecule results in greatly reduced bond strengths. Due to the delocalised nature of the charge, all bonds are weakened equally. The mass spectra of unbranched alkanes show groups of ions separated by 14Da. This separation is ...
Chemistry Lesson 40 Organic Chemistry
... g. Some compounds have more than one functional group – such as amino acids, which contain an amine (C-N) group and an organic acid (COOH) group. h. Naming organic compounds with functional groups involves using the alkane name, and adding the prefix/suffix for the functional group. ...
... g. Some compounds have more than one functional group – such as amino acids, which contain an amine (C-N) group and an organic acid (COOH) group. h. Naming organic compounds with functional groups involves using the alkane name, and adding the prefix/suffix for the functional group. ...
aldehydes powerpoint
... beans their aroma. (Often appears in nature) • Cinnamaldehyde smells like cinnamon. ...
... beans their aroma. (Often appears in nature) • Cinnamaldehyde smells like cinnamon. ...
level three chemistry: organics
... I can show that I understand the significance of the structure of each functional group by explaining the relative solubility of each functional group in terms of polarity and hydrogen bonding. I can show that I understand the significance of the structure of each functional group by explaining the ...
... I can show that I understand the significance of the structure of each functional group by explaining the relative solubility of each functional group in terms of polarity and hydrogen bonding. I can show that I understand the significance of the structure of each functional group by explaining the ...
Introduction to Organic Chemistry
... organic material but did not exist in any inorganic materials. 4. What did Friedrich Wöhler have to do with discrediting the “vital force” theory? 1. He was widely regarded as a pioneer in organic chemistry as a result of his synthesizing of the biological compound urea (a component of urine in many ...
... organic material but did not exist in any inorganic materials. 4. What did Friedrich Wöhler have to do with discrediting the “vital force” theory? 1. He was widely regarded as a pioneer in organic chemistry as a result of his synthesizing of the biological compound urea (a component of urine in many ...
8.2-Organic Nomenclature packet
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
Nomenclature
... • Their physical properties are similar to alkanes of comparable molecular weight. • Alkenes have low melting points and boiling points. • M.p. and b.p. increase as the number of carbons increases because of increased surface area. • Alkenes are soluble in organic solvents and insoluble in water. • ...
... • Their physical properties are similar to alkanes of comparable molecular weight. • Alkenes have low melting points and boiling points. • M.p. and b.p. increase as the number of carbons increases because of increased surface area. • Alkenes are soluble in organic solvents and insoluble in water. • ...
Edexcel GCE - The Student Room
... (c) Lithium can react with chlorine to produce lithium chloride. When a sample of lithium chloride is heated in a Bunsen flame, a red colour is seen. (i) Draw a ‘dot and cross’ diagram of lithium chloride showing all the electrons. Indicate the charges clearly on your diagram. ...
... (c) Lithium can react with chlorine to produce lithium chloride. When a sample of lithium chloride is heated in a Bunsen flame, a red colour is seen. (i) Draw a ‘dot and cross’ diagram of lithium chloride showing all the electrons. Indicate the charges clearly on your diagram. ...
A Level Chemistry A Lesson Element Keyword activities
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... We’d like to know your view on the resources we produce. By clicking on the ‘Like’ or ‘Dislike’ button you can help us to ensure that our resources work for you. When the email template pops up please add additional comments if you wish and then just click ‘Send’. Thank you. If you do not currently ...
Organic_Nomenclature_packet
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
Organic Nomenclature - Alkanes, Alkenes, Alkynes
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
... Hydrocarbons that contain multiple bonds are called unsaturated hydrocarbons. If the hydrocarbon has one double bond, its general formula will be CnH2n, where n is the number of carbon atoms in the compound. The alkene family uses the -ene ending. The double bond is stronger than a single bond, and ...
45.1 Inter-conversions between the functional groups
... [R] – 1. LiAlH4, dry ether 2. H+(aq) [R] – NaBH4, water * ∆ = heat ...
... [R] – 1. LiAlH4, dry ether 2. H+(aq) [R] – NaBH4, water * ∆ = heat ...
Organic Functional Groups: Aldehydes, Ketones, Acids, Esters
... similar sized alcohols. • Their boiling points are thus lower than alcohols. • They are good solvents for both polar and non-polar substances. • The oxygen is fairly reactive, and many of these compounds are toxic, carcinogenic. ...
... similar sized alcohols. • Their boiling points are thus lower than alcohols. • They are good solvents for both polar and non-polar substances. • The oxygen is fairly reactive, and many of these compounds are toxic, carcinogenic. ...
Organometallic Chemistry
... Metal carbonyls can be made in a variety of ways. For Ni and Fe, the homoleptic or binary metal carbonyls can be made by the direct interaction with the metal (Equation 1). In other cases, a reduction of a metal precursor in the presence of CO (or using CO as the reductant) is used (Equations 2-3). ...
... Metal carbonyls can be made in a variety of ways. For Ni and Fe, the homoleptic or binary metal carbonyls can be made by the direct interaction with the metal (Equation 1). In other cases, a reduction of a metal precursor in the presence of CO (or using CO as the reductant) is used (Equations 2-3). ...
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.