Groups 2 and 7
... The reactions of sodium halides with concentrated sulfuric acid demonstrate the relative strengths of the halide ions as reducing agents. 76 of 43 ...
... The reactions of sodium halides with concentrated sulfuric acid demonstrate the relative strengths of the halide ions as reducing agents. 76 of 43 ...
No Slide Title
... 4.4 Families of Organic Compounds—Functional Groups, Continued Aromatics • Unsaturated cyclic compounds like benzene, which are unusually stable, are said to exhibit aromaticity. • Stability of the double bonds of benzene is due to the fact that the double bonds are not static. That is, the electro ...
... 4.4 Families of Organic Compounds—Functional Groups, Continued Aromatics • Unsaturated cyclic compounds like benzene, which are unusually stable, are said to exhibit aromaticity. • Stability of the double bonds of benzene is due to the fact that the double bonds are not static. That is, the electro ...
Grignard Reaction - OpenBU
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
Grignard Reaction - Synthesis of Substituted Benzoic Acids
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
Grignard Reaction - OpenBU
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
... polarized, placing a partial negative charge on the carbon directly attached to the metal. The magnesium itself had a partial positive charge and the bromide has a partial negative charge. Mgo R ...
Hydrocarbons
... IUPAC name - The OH group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “ol” ...
... IUPAC name - The OH group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “ol” ...
An Introduction to Organic Compounds: Nomenclature
... IUPAC name - The OH group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “ol” ...
... IUPAC name - The OH group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “ol” ...
SAMPLE PROBLEM
... Another feasible stereoselective retrosynthesis involves net addition of two nitrogen atoms across the double bond which should generate structure 8 from 9.1 The diastereoselectivity is controlled at this point but there will be a racemic mixture (two enantiomers in the reaction vessel) once the syn ...
... Another feasible stereoselective retrosynthesis involves net addition of two nitrogen atoms across the double bond which should generate structure 8 from 9.1 The diastereoselectivity is controlled at this point but there will be a racemic mixture (two enantiomers in the reaction vessel) once the syn ...
Organic Chemistry Introduction
... Reactions of Alkynes • Alkynes are rare in biological chemistry • Chemistry is similar to alkenes • Generally less reactive than alkenes • Reactions can be stopped at alkene stage using one equivalent of the reagent ...
... Reactions of Alkynes • Alkynes are rare in biological chemistry • Chemistry is similar to alkenes • Generally less reactive than alkenes • Reactions can be stopped at alkene stage using one equivalent of the reagent ...
Chlorine chemistry revised 28 Jan 2017
... •Chlorine has the highest electron affinity (348.6 kJ/mol) and the third highest electronegativity (3.16) of all the reactive elements. The Cl-Cl bond dissociation energy (58 kcal/mol) is the highest among dihalogen molecules. •Chlorine gas and many of its compounds are chemicals useful in water pu ...
... •Chlorine has the highest electron affinity (348.6 kJ/mol) and the third highest electronegativity (3.16) of all the reactive elements. The Cl-Cl bond dissociation energy (58 kcal/mol) is the highest among dihalogen molecules. •Chlorine gas and many of its compounds are chemicals useful in water pu ...
22. Oxidation of Cyclohexanol
... Oxidation-reduction reactions play an important role in organic chemistry. Oxidation of alcohols to form aldehydes, ketones or carboxylic acids is a fundamental and widely used reaction. Primary alcohols can be oxidized to aldehydes or carboxylic acids while secondary alcohols oxidize to ketones. Te ...
... Oxidation-reduction reactions play an important role in organic chemistry. Oxidation of alcohols to form aldehydes, ketones or carboxylic acids is a fundamental and widely used reaction. Primary alcohols can be oxidized to aldehydes or carboxylic acids while secondary alcohols oxidize to ketones. Te ...
Ordinary Level - State Examination Commission
... Why is electrical power transmitted at high voltages over long distances? ...
... Why is electrical power transmitted at high voltages over long distances? ...
CHE-310 Organic Chemistry I_
... For alkyl halides, alcohols and ethers, be able to name compounds correctly (nomenclature). Where necessay, be able to specify congiguration in the name. Know the two new mechanisms that we have learned in these chapters: SN2, SN1. Know which mechanisms go with which reactions under which conditions ...
... For alkyl halides, alcohols and ethers, be able to name compounds correctly (nomenclature). Where necessay, be able to specify congiguration in the name. Know the two new mechanisms that we have learned in these chapters: SN2, SN1. Know which mechanisms go with which reactions under which conditions ...
this file - CBE Project Server
... ❏ optical activity ❏ SN1 and SN2 ❏ primary carbon cation ❏ carbanion ❏ Markovnikov's Rule ❏ nucleophilic ❏ ortho, meta, para ❏ alcohol ...
... ❏ optical activity ❏ SN1 and SN2 ❏ primary carbon cation ❏ carbanion ❏ Markovnikov's Rule ❏ nucleophilic ❏ ortho, meta, para ❏ alcohol ...
Introduction, Alkanes and Structural Isomers
... A student draws these structures as examples of structural isomers of C7H16. How many unique structural isomers are shown? (In other words, which structures are the same as another structure?) (Tip: If they have the same name, the structure is the same!) ...
... A student draws these structures as examples of structural isomers of C7H16. How many unique structural isomers are shown? (In other words, which structures are the same as another structure?) (Tip: If they have the same name, the structure is the same!) ...
Organic Chemistry – Summary of Reactions and Conditions
... heat to 170C Where several products are possible, those in which the carbon atoms of the double bond contain most alkyl groups are favoured. Conversion to halogenoalkane Reaction type: Substitution ...
... heat to 170C Where several products are possible, those in which the carbon atoms of the double bond contain most alkyl groups are favoured. Conversion to halogenoalkane Reaction type: Substitution ...
Aldehydes and Ketones
... NAMING ALDEHYDES • ALDEHYDES ARE NAMED BY REPLACING THE FINAL “E” OF THE NAME OF THE ALKANE WITH THE SAME NUMBER OF CARBONS TO “AL”. • BECAUSE IN ALDEHYDES THE CARBONYL GROUP IS ALWAYS ATTACHED TO THE FIRST CARBON, THERE IS NO NEED TO PLACE A 1 IN FRONT OF THE NAME. • IF THERE ARE SUBSTITUENTS PRES ...
... NAMING ALDEHYDES • ALDEHYDES ARE NAMED BY REPLACING THE FINAL “E” OF THE NAME OF THE ALKANE WITH THE SAME NUMBER OF CARBONS TO “AL”. • BECAUSE IN ALDEHYDES THE CARBONYL GROUP IS ALWAYS ATTACHED TO THE FIRST CARBON, THERE IS NO NEED TO PLACE A 1 IN FRONT OF THE NAME. • IF THERE ARE SUBSTITUENTS PRES ...
An Introduction to Organic Chemistry
... The first step is homolytic fission of the halogen to produce halide radicals. This is termed the intitiation step, [I]. Radicals are extremely reactive species with single unpaired electrons denoted ·. Radicals react with non-radical and radical species in propagation and termination steps, [P] and ...
... The first step is homolytic fission of the halogen to produce halide radicals. This is termed the intitiation step, [I]. Radicals are extremely reactive species with single unpaired electrons denoted ·. Radicals react with non-radical and radical species in propagation and termination steps, [P] and ...
Activity 1: Chapter 1: Carbon Compounds and Chemical Bonds
... Alkyl halide = a hydrocarbon having at least one halide connected to a carbon atom. Alkene = a hydrocarbon having at least one double bond between carbon atoms. Alkyne = a hydrocarbon having at least one triple bond between carbon atoms. Alcohol = a hydrocarbon containing an “O-H” functional group c ...
... Alkyl halide = a hydrocarbon having at least one halide connected to a carbon atom. Alkene = a hydrocarbon having at least one double bond between carbon atoms. Alkyne = a hydrocarbon having at least one triple bond between carbon atoms. Alcohol = a hydrocarbon containing an “O-H” functional group c ...
Alcohols and Phenols
... Reactions of Esters and Grignard Reagents • Yields tertiary alcohols in which two of the substituents carbon come from the Grignard reagent • Grignard reagents do not add to carboxylic acids – they undergo an acid-base reaction, generating the hydrocarbon of the Grignard reagent ...
... Reactions of Esters and Grignard Reagents • Yields tertiary alcohols in which two of the substituents carbon come from the Grignard reagent • Grignard reagents do not add to carboxylic acids – they undergo an acid-base reaction, generating the hydrocarbon of the Grignard reagent ...
United States Patent Boyle et aI.
... through Rs have the members necessary to make a porphyrin. chlorin. bacteriochlorin. benzochlorin, hydroxychlorin or hydroxybacteriochlorin nucleus. S1 through S3 are the same or different and can be H. any one of a large number of substituted or unsubstituted alkyl groups, substituted or un substit ...
... through Rs have the members necessary to make a porphyrin. chlorin. bacteriochlorin. benzochlorin, hydroxychlorin or hydroxybacteriochlorin nucleus. S1 through S3 are the same or different and can be H. any one of a large number of substituted or unsubstituted alkyl groups, substituted or un substit ...
Workshop #1 Part 1. Organic Chemistry Nomenclature
... Alkyl halide = a hydrocarbon having at least one halide connected to a carbon atom. Alkene = a hydrocarbon having at least one double bond between carbon atoms. Alkyne = a hydrocarbon having at least one triple bond between carbon atoms. Alcohol = a hydrocarbon containing an “O-H” functional group c ...
... Alkyl halide = a hydrocarbon having at least one halide connected to a carbon atom. Alkene = a hydrocarbon having at least one double bond between carbon atoms. Alkyne = a hydrocarbon having at least one triple bond between carbon atoms. Alcohol = a hydrocarbon containing an “O-H” functional group c ...
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.