ORGANIC MOLECULES 25 FEBRUARY 2014
... An organic molecule is a compound that contains carbon atoms. Hydrocarbons are organic molecules that contain carbon and hydrogen atoms. A homologous series is a series of compounds that have the same functional group and are described by the same general formula. The consecutive members of the seri ...
... An organic molecule is a compound that contains carbon atoms. Hydrocarbons are organic molecules that contain carbon and hydrogen atoms. A homologous series is a series of compounds that have the same functional group and are described by the same general formula. The consecutive members of the seri ...
- EdShare - University of Southampton
... Alkenes are unsaturated compounds that can be used in organic synthesis. They can be formed in elimination reactions of halogenoalkanes. An example of this is the reaction between 2-bromopentane and hot ethanolic KOH. Using your knowledge of reaction mechanisms, draw appropriate curly arrows to comp ...
... Alkenes are unsaturated compounds that can be used in organic synthesis. They can be formed in elimination reactions of halogenoalkanes. An example of this is the reaction between 2-bromopentane and hot ethanolic KOH. Using your knowledge of reaction mechanisms, draw appropriate curly arrows to comp ...
- EdShare - University of Southampton
... Draw the mechanism of the reaction between CH3CH2CH2Br and hot KOH(aq) using the curly arrow model. State the name of the mechanism, and include any relevant dipoles. ...
... Draw the mechanism of the reaction between CH3CH2CH2Br and hot KOH(aq) using the curly arrow model. State the name of the mechanism, and include any relevant dipoles. ...
Professor Marina Gatti
... interest: pyrrole, furan, thiophene, indole, imidazole, pyridine, pyrimidine, purine.. Overview of polycyclic aromatic hydrocarbons. Mechanism of electrophilic aromatic substitution. Monosubstituted benzenes: effect of substituents on substitution rate and orientation. ...
... interest: pyrrole, furan, thiophene, indole, imidazole, pyridine, pyrimidine, purine.. Overview of polycyclic aromatic hydrocarbons. Mechanism of electrophilic aromatic substitution. Monosubstituted benzenes: effect of substituents on substitution rate and orientation. ...
CHE-05 year 2004
... Suggest the structure of the alkene/diene that give the following products: i) ...
... Suggest the structure of the alkene/diene that give the following products: i) ...
ALKENES and SULPHURIC ACID
... The structure of the product molecule is sometimes written as CH3CH2HSO4, but the version in the equation is better because it shows how all the atoms are linked up. You may also find it written as CH3CH2OSO3H. Confused by all this? Don't be! All you need to do is to learn the structure of sulphuric ...
... The structure of the product molecule is sometimes written as CH3CH2HSO4, but the version in the equation is better because it shows how all the atoms are linked up. You may also find it written as CH3CH2OSO3H. Confused by all this? Don't be! All you need to do is to learn the structure of sulphuric ...
Double bonds
... Can form hydrogen bonds with water molecules, helping dissolve organic compounds such as sugars. ...
... Can form hydrogen bonds with water molecules, helping dissolve organic compounds such as sugars. ...
organic chemistry - Peoria Public Schools
... unstable and reactive; such a particle with an unpaired electron is called a free radical * free radicals have a strong tendency to react and usually have a short existence; tend to be intermediates in reactions A B ...
... unstable and reactive; such a particle with an unpaired electron is called a free radical * free radicals have a strong tendency to react and usually have a short existence; tend to be intermediates in reactions A B ...
Ch.14
... • Oxidation occurs only with strong oxidizing agents. • Halogenation • Weak acids in solution (Ka~10-10) ...
... • Oxidation occurs only with strong oxidizing agents. • Halogenation • Weak acids in solution (Ka~10-10) ...
Organic/Biological Chemistry
... 1. Find longest continuous chain of carbon atoms, and use name of this chain (see Table 25.1) as the base name of the compound. 2. Number the carbon atoms in the longest chain, beginning with end of chain that is nearest to a substituent. 3. Name and give the location of each substituent group. 4. W ...
... 1. Find longest continuous chain of carbon atoms, and use name of this chain (see Table 25.1) as the base name of the compound. 2. Number the carbon atoms in the longest chain, beginning with end of chain that is nearest to a substituent. 3. Name and give the location of each substituent group. 4. W ...
Chapter 18 Notes (Word), Part II File
... Recall: halogens are group 17 on the periodic table (F, Cl, Br. I) X = F, Br, Cl or I NAMING halocarbons Name the halogens as branches off the main carbon chain The halogens are prefixes (fluoro-, chloro-, bromo-, iodo-) to the hydrocarbon name Use numbers to indicate the halogen position( ...
... Recall: halogens are group 17 on the periodic table (F, Cl, Br. I) X = F, Br, Cl or I NAMING halocarbons Name the halogens as branches off the main carbon chain The halogens are prefixes (fluoro-, chloro-, bromo-, iodo-) to the hydrocarbon name Use numbers to indicate the halogen position( ...
Alcohols, Ethers and Epoxides Alcohols contain a hydroxy group (OH)
... • For an alcohol to undergo nucleophilic substitution, OH must be converted into a better leaving group. By using acid, ¯OH can be converted into H2O, a good leaving group. ...
... • For an alcohol to undergo nucleophilic substitution, OH must be converted into a better leaving group. By using acid, ¯OH can be converted into H2O, a good leaving group. ...
Ch 26 C-C bond formation
... • To form the carbon skeletons of complex molecules, organic chemists need an extensive repertoire of carbon–carbon bond forming reactions. • We have earlier looked at reactions of organometallic reagents such as Grignard, organolithium and organocuprate reagents with carbonyl and other substrates t ...
... • To form the carbon skeletons of complex molecules, organic chemists need an extensive repertoire of carbon–carbon bond forming reactions. • We have earlier looked at reactions of organometallic reagents such as Grignard, organolithium and organocuprate reagents with carbonyl and other substrates t ...
organic outline - No Brain Too Small
... All swap OH group for Cl atom. SOCl2 is the best one!! To form carboxylic acids with MnO4-/H+, heat (purple MnO4turns to colourless Mn2+) or Cr2O72-/H+, heat (orange Cr2O72- turns to green Cr3+) Also combustion (also oxidation reaction) as alcohols make good fuels, burning cleanly (complete combus ...
... All swap OH group for Cl atom. SOCl2 is the best one!! To form carboxylic acids with MnO4-/H+, heat (purple MnO4turns to colourless Mn2+) or Cr2O72-/H+, heat (orange Cr2O72- turns to green Cr3+) Also combustion (also oxidation reaction) as alcohols make good fuels, burning cleanly (complete combus ...
Review (Chapter 1) 1) Indicate if the following statements are true
... ) double headed arrows are used to indicate reversable reactions ) The carbon in tetrabromomethane is SP4 hybridized ) The carbon-carbon bond in propane is formed from Sp3 and S orbitals ) Cyclic organic compounds contains always heteroatoms ) Alkanes have only one double bond ...
... ) double headed arrows are used to indicate reversable reactions ) The carbon in tetrabromomethane is SP4 hybridized ) The carbon-carbon bond in propane is formed from Sp3 and S orbitals ) Cyclic organic compounds contains always heteroatoms ) Alkanes have only one double bond ...
Optical Isomers or Enantiomers
... • 20.2.2 Describe and explain how the rate of nucleophilic substitution in halogenoalkanes by the hydroxide ion depends on the identity of the halogen. • 20.2.3 Describe and explain how the rate of nucleophilic substitution in halogenoalkanes by the hydroxide ion depends on whether the halogenoalkan ...
... • 20.2.2 Describe and explain how the rate of nucleophilic substitution in halogenoalkanes by the hydroxide ion depends on the identity of the halogen. • 20.2.3 Describe and explain how the rate of nucleophilic substitution in halogenoalkanes by the hydroxide ion depends on whether the halogenoalkan ...
10 Introduction to organic chemistry
... 9 In the reaction between ethene and bromine, bromine attacks the electron-rich π-bond. In ethane, all the bonds are σ-bonds, so there is no centre of high-electron density. The propagation step of the photochemical substitution reaction with ethane involves the reaction of a bromine radical with an ...
... 9 In the reaction between ethene and bromine, bromine attacks the electron-rich π-bond. In ethane, all the bonds are σ-bonds, so there is no centre of high-electron density. The propagation step of the photochemical substitution reaction with ethane involves the reaction of a bromine radical with an ...
Nucleophilic Substitution Reactions of Epoxides
... • Primary: No reaction SN2 and SN1 • Secondary: Reaction in ~5 minutes • Tertiary, allylic, and benzylic: Reaction immediate ...
... • Primary: No reaction SN2 and SN1 • Secondary: Reaction in ~5 minutes • Tertiary, allylic, and benzylic: Reaction immediate ...
Structure and Bonding
... Alkenes – cis andb trans isomerism The cis and trans isomers of an alkene are configurational isomers (also called geometric isomers) because they have different shapes and cannot interconvert since the double bond of an alkene cannot rotate. Therefore, the substituents are ‘fixed’ in space relativ ...
... Alkenes – cis andb trans isomerism The cis and trans isomers of an alkene are configurational isomers (also called geometric isomers) because they have different shapes and cannot interconvert since the double bond of an alkene cannot rotate. Therefore, the substituents are ‘fixed’ in space relativ ...
Haloalkanes
... The Environmental problems associated with CFC Because of the lack of reactivity and insolubility in water, there is no natural process for removing CFC. In fact they drift up into the stratosphere (the upper atmosphere), where they receive sufficient ultraviolet Light to cause photolysis. The chlor ...
... The Environmental problems associated with CFC Because of the lack of reactivity and insolubility in water, there is no natural process for removing CFC. In fact they drift up into the stratosphere (the upper atmosphere), where they receive sufficient ultraviolet Light to cause photolysis. The chlor ...
Alkanes
... In a benzene molecule, the bonding electrons between carbon atoms are shared evenly around the ring. An aromatic compound is an organic compound that contains a ______ ring or other ring in which the bonding is like that of ...
... In a benzene molecule, the bonding electrons between carbon atoms are shared evenly around the ring. An aromatic compound is an organic compound that contains a ______ ring or other ring in which the bonding is like that of ...
Organic Reactions
... • Isomers have the same molecular formula, empirical formula, and % composition. They test this definition a lot. • If you’re not sure about an isomer, count the carbons, hydrogens, and oxygens; make sure they’re the same as the molecule in question. ...
... • Isomers have the same molecular formula, empirical formula, and % composition. They test this definition a lot. • If you’re not sure about an isomer, count the carbons, hydrogens, and oxygens; make sure they’re the same as the molecule in question. ...
PowerPoint for Part 1 - Dr. Samples` Chemistry Classes
... Functional Groups with Carbon Singly Bonded to an Electronegative Atom • Carbon is quite commonly bonded to an electronegative atom like O, N, Cl, Br, I, F, or S. • Alkyl halides have C bonded to a halogen; ethers, alcohols have C bonded to O; amines have C bonded to N; and thiols have C bonded to ...
... Functional Groups with Carbon Singly Bonded to an Electronegative Atom • Carbon is quite commonly bonded to an electronegative atom like O, N, Cl, Br, I, F, or S. • Alkyl halides have C bonded to a halogen; ethers, alcohols have C bonded to O; amines have C bonded to N; and thiols have C bonded to ...
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.