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... ie for an alkane: CnH2n+2, (iv) structural formula as the minimal detail that shows the arrangement of atoms in a molecule, eg for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3, (v) displayed formula as the relative positioning of atoms and the bonds between them (vi) skeletal formula as the simplified organ ...
... ie for an alkane: CnH2n+2, (iv) structural formula as the minimal detail that shows the arrangement of atoms in a molecule, eg for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3, (v) displayed formula as the relative positioning of atoms and the bonds between them (vi) skeletal formula as the simplified organ ...
Question paper - Edexcel
... be allowed to subside after each addition. 4. After the addition of iodine is complete, the mixture is heated under reflux for 30 – 60 minutes, until little or no iodine is visible. 5. The apparatus is allowed to cool and the condenser rearranged for distillation. 6. The crude 1-iodobutane is distil ...
... be allowed to subside after each addition. 4. After the addition of iodine is complete, the mixture is heated under reflux for 30 – 60 minutes, until little or no iodine is visible. 5. The apparatus is allowed to cool and the condenser rearranged for distillation. 6. The crude 1-iodobutane is distil ...
Document
... Sterically hindered alcohols also react more slowly in the esterification reaction. The relative rates for esterification of alcohols with acetic acid follow the order: ...
... Sterically hindered alcohols also react more slowly in the esterification reaction. The relative rates for esterification of alcohols with acetic acid follow the order: ...
The carbonyl group
... Physical properties • The carbonyl group is a strong dipole. This causes the B.P of aldehydes and ketones to be higher than similar molecular weight alkanes and others but lower than alcohols which are held together by H-bonds. Aldehyde < Alcohols > Alkane ...
... Physical properties • The carbonyl group is a strong dipole. This causes the B.P of aldehydes and ketones to be higher than similar molecular weight alkanes and others but lower than alcohols which are held together by H-bonds. Aldehyde < Alcohols > Alkane ...
Review Questions
... VESPR theory-know the shapes [linear, trigonal planar, tetrahedral, pyramidal, bent, trigonal bipyramidal, octahedral, square planar Orbitals: s, p, d, f and hybridized orbitals sp, sp2, sp3 Formation of single, double and triple bonds Problems: 1. Draw Lewis Structure for each of the followin ...
... VESPR theory-know the shapes [linear, trigonal planar, tetrahedral, pyramidal, bent, trigonal bipyramidal, octahedral, square planar Orbitals: s, p, d, f and hybridized orbitals sp, sp2, sp3 Formation of single, double and triple bonds Problems: 1. Draw Lewis Structure for each of the followin ...
CARBON AND ITS COMPOUNDS
... H2O: -Atomic number of O is 8. Its electronic configuration is 2,6 and thus requires two electrons to complete its octet (8). Atomic number of H is 1. Its electronic configuration is 1 and thus requires 1 electron to complete the K shell.(duplet) Thus O shares two of its valence electrons with each ...
... H2O: -Atomic number of O is 8. Its electronic configuration is 2,6 and thus requires two electrons to complete its octet (8). Atomic number of H is 1. Its electronic configuration is 1 and thus requires 1 electron to complete the K shell.(duplet) Thus O shares two of its valence electrons with each ...
ether - TeacherWeb
... Intermolecular Forces in Ethers • Ethers lack the hydroxyl group that alcohols have, preventing them from having any type of hydrogen bonding. • However, the C-O bond is polar, thus, ether molecules are somewhat polar, just not as polar as alcohols. • The intermolecular forces in ethers are stron ...
... Intermolecular Forces in Ethers • Ethers lack the hydroxyl group that alcohols have, preventing them from having any type of hydrogen bonding. • However, the C-O bond is polar, thus, ether molecules are somewhat polar, just not as polar as alcohols. • The intermolecular forces in ethers are stron ...
Demonstrate skill in organic chemistry techniques.
... Discuss the physical properties of alcohols and summarize the methods used to synthesize them. Learning Objectives Draw structures and name alcohols, phenols, diols, and thiols. Predict relative boiling points, acidities, and solubilities. Show the conversion of alcohols from alkenes, alkyl halides, ...
... Discuss the physical properties of alcohols and summarize the methods used to synthesize them. Learning Objectives Draw structures and name alcohols, phenols, diols, and thiols. Predict relative boiling points, acidities, and solubilities. Show the conversion of alcohols from alkenes, alkyl halides, ...
Addition/elimination under acidic conditions
... Nucleophilic acyl substitutions can occur with weak nucleophiles under basic conditions, but only if the carboxylic acid derivative is very reactive Nulceophilic acyl substitutions can occur with weak nucleophiles under acidic conditions Carboxylic acids can be esterified with alcohols under a ...
... Nucleophilic acyl substitutions can occur with weak nucleophiles under basic conditions, but only if the carboxylic acid derivative is very reactive Nulceophilic acyl substitutions can occur with weak nucleophiles under acidic conditions Carboxylic acids can be esterified with alcohols under a ...
CHEMISTRY 3.5 Paper 1 Describe the structure and reactions of
... acidic conditions, the amino acid forms an ion that will move towards one electrode. In basic conditions, it forms another ion that will move towards the other electrode. Explain how the conditions described above give rise to two ions that will move towards the two different electrodes and state wh ...
... acidic conditions, the amino acid forms an ion that will move towards one electrode. In basic conditions, it forms another ion that will move towards the other electrode. Explain how the conditions described above give rise to two ions that will move towards the two different electrodes and state wh ...
June 6 – Alcohols - hrsbstaff.ednet.ns.ca
... only one other carbon • Secondary – the hydroxyl group is bonded to a carbon that is bonded to two other carbons • Tertiary – the hydroxyl group is bonded to a carbon that is bonded to three other carbons ...
... only one other carbon • Secondary – the hydroxyl group is bonded to a carbon that is bonded to two other carbons • Tertiary – the hydroxyl group is bonded to a carbon that is bonded to three other carbons ...
Screening - Entrance
... 8. An alkene (A) C16H16 on ozonolysis gives only one product (B) C8H8O. Compound (B) on reaction with NaOH/I2 yields sodium benzoate. Compound (B) reacts with KOH/NH2NH2 yielding a hydrocarbon (C) C8H10. Write the structures of compounds (B) and (C). Based on this information two isomeric structures ...
... 8. An alkene (A) C16H16 on ozonolysis gives only one product (B) C8H8O. Compound (B) on reaction with NaOH/I2 yields sodium benzoate. Compound (B) reacts with KOH/NH2NH2 yielding a hydrocarbon (C) C8H10. Write the structures of compounds (B) and (C). Based on this information two isomeric structures ...
Organic Nomenclature Notes
... metals, etc, and organic: plant life, animals, plastics, etc. The simplest organic compounds are made up of only two elements: carbon and hydrogen. Compounds such as these are called hydrocarbons. There is an extremely large number of hydrocarbons known to science. As a result, a classification sche ...
... metals, etc, and organic: plant life, animals, plastics, etc. The simplest organic compounds are made up of only two elements: carbon and hydrogen. Compounds such as these are called hydrocarbons. There is an extremely large number of hydrocarbons known to science. As a result, a classification sche ...
TV RajanBabu Chemistry, 730 Autumn 1997
... Michael reaction - stabilized enolates- malonates, acetoacetates, nitronates Michael reaction of kinetic enolates -special acceptors ...
... Michael reaction - stabilized enolates- malonates, acetoacetates, nitronates Michael reaction of kinetic enolates -special acceptors ...
Reacciones redox
... Because the reaction follows an SN2 mechanism: • Unhindered CH3X and 1° R-X are more easily reduced than more substituted 2°and 3° halides. • In unsymmetrical epoxides, nucleophilic attack of H– (from LiAlH4) occurs at the less substituted ...
... Because the reaction follows an SN2 mechanism: • Unhindered CH3X and 1° R-X are more easily reduced than more substituted 2°and 3° halides. • In unsymmetrical epoxides, nucleophilic attack of H– (from LiAlH4) occurs at the less substituted ...
Derivatives of Carboxylic Acids
... • Salicylic acid is a bifunctional molecule (acid and phenol) which is itself a disinfectant. • Aspirin comes from the willow bark which was used in the Middle Ages by Jesuit missionaries. ...
... • Salicylic acid is a bifunctional molecule (acid and phenol) which is itself a disinfectant. • Aspirin comes from the willow bark which was used in the Middle Ages by Jesuit missionaries. ...
Slide 1
... • Ammonia and primary amines initially react with carboxylic acids to form a salt of the acid, but if this is heated it dehydrates to form an amide. • If ethanoic acid is reacted with methylamine, and the initially formed methylammonium ethanoate is heated, then N-methylethanamide is formed: ...
... • Ammonia and primary amines initially react with carboxylic acids to form a salt of the acid, but if this is heated it dehydrates to form an amide. • If ethanoic acid is reacted with methylamine, and the initially formed methylammonium ethanoate is heated, then N-methylethanamide is formed: ...
Identification of Unknown Organic Compounds
... Halogens can be detected easily and reliably by the Beilstein test. It is the simplest method for determining the presence of a halogen, but does not differentiate among chlorine, bromine, and iodine. A positive Beilstein test results from the production of a volatile copper halide when an organic h ...
... Halogens can be detected easily and reliably by the Beilstein test. It is the simplest method for determining the presence of a halogen, but does not differentiate among chlorine, bromine, and iodine. A positive Beilstein test results from the production of a volatile copper halide when an organic h ...
Organic Chemistry
... Organic chemistry is the branch of chemistry that deals with the study of carbon based compounds. Bonds between carbon atoms are covalent; each carbon is capable of forming four bonds: ...
... Organic chemistry is the branch of chemistry that deals with the study of carbon based compounds. Bonds between carbon atoms are covalent; each carbon is capable of forming four bonds: ...
Molecular Orbitals - Calderglen High School
... Boiling Points—most organic molecules contain mainly hydrogen and carbon. As the hydrocarbon chain increases in these molecules the strength of London dispersion forces also increases giving rise to a higher boiling point. As a result more energy is require to move the molecules further apart. Branc ...
... Boiling Points—most organic molecules contain mainly hydrogen and carbon. As the hydrocarbon chain increases in these molecules the strength of London dispersion forces also increases giving rise to a higher boiling point. As a result more energy is require to move the molecules further apart. Branc ...
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.