ORGANIC CHEMISTRY I – REVIEW FOR FINAL EXAM
... Addition of Halogens to Alkenes Halohydrin Formation Addition of Water to Alkenes: Oxymercuration, and Hydroboration Addition of Carbenes to Alkenes: Cyclopropane Synthesis Reduction of Alkenes: Hydrogenation Oxidation of Alkenes: Hydroxylation and Cleavage ...
... Addition of Halogens to Alkenes Halohydrin Formation Addition of Water to Alkenes: Oxymercuration, and Hydroboration Addition of Carbenes to Alkenes: Cyclopropane Synthesis Reduction of Alkenes: Hydrogenation Oxidation of Alkenes: Hydroxylation and Cleavage ...
Notes 07 Organometallic Compounds with notes
... Examples of M include Li, Mg (Grignard reagents), Na, Cu, and Zn. Nucleophilic carbon: Reacts with electrophilic carbon and forms a new carbon-carbon bond. ...
... Examples of M include Li, Mg (Grignard reagents), Na, Cu, and Zn. Nucleophilic carbon: Reacts with electrophilic carbon and forms a new carbon-carbon bond. ...
Organic chemistry - Mr. Amundson`s DCC science
... OH group increases polarity. Combust easily Primary, secondary and tertiary alcohols Primary alcohols become aldehydes and carboxylic acid under oxidation Secondary alcohols become ketones under oxidation. Tertiary alcohols don’t oxidize. ...
... OH group increases polarity. Combust easily Primary, secondary and tertiary alcohols Primary alcohols become aldehydes and carboxylic acid under oxidation Secondary alcohols become ketones under oxidation. Tertiary alcohols don’t oxidize. ...
Intro to organic chemistry (orgo)
... • General rule: H atom most likely to be removed from C atom with most C-C bonds • “The poor get poorer!” ▫ opposite of Markovnikov’s Rule ▫ Called Zaitsev’s rule ...
... • General rule: H atom most likely to be removed from C atom with most C-C bonds • “The poor get poorer!” ▫ opposite of Markovnikov’s Rule ▫ Called Zaitsev’s rule ...
+ Y
... has an electron-poor atom (e.g H+, CH3+ ) and can form a bond by accepting a pair of electrons from a nucleophile ...
... has an electron-poor atom (e.g H+, CH3+ ) and can form a bond by accepting a pair of electrons from a nucleophile ...
1 - contentextra
... Nomenclature A precise means of naming entities so that they can be communicated nonambiguously. Organic chemistry uses the system of IUPAC nomenclature. Nucleophile An electron-rich species that is therefore attracted to parts of molecules that are electron deficient. Nucleophiles have a lone pair ...
... Nomenclature A precise means of naming entities so that they can be communicated nonambiguously. Organic chemistry uses the system of IUPAC nomenclature. Nucleophile An electron-rich species that is therefore attracted to parts of molecules that are electron deficient. Nucleophiles have a lone pair ...
Functional Groups PP
... 2. Which of the following is an alkane (single bonds only)? Which is an alkene (double bond)? An alkyne (triple bond)? 1. C2H6 2. C2H4 3. C2H2 ...
... 2. Which of the following is an alkane (single bonds only)? Which is an alkene (double bond)? An alkyne (triple bond)? 1. C2H6 2. C2H4 3. C2H2 ...
90309 Describe the structural formulae and reactions of compounds
... Larger organic molecules may be used in questions involving the linking of structure and reactivity. ...
... Larger organic molecules may be used in questions involving the linking of structure and reactivity. ...
Organic Objectives
... draw isomers of molecules and recognize isomers. write the formula of a hydrocarbon, given its name and vice versa. give household examples of hydrocarbons (methane, ethane, propane, butane, octane). identify the “parent chain” looking at a structural formula give examples of substituted h ...
... draw isomers of molecules and recognize isomers. write the formula of a hydrocarbon, given its name and vice versa. give household examples of hydrocarbons (methane, ethane, propane, butane, octane). identify the “parent chain” looking at a structural formula give examples of substituted h ...
Worksheet – Alkanes Alkanes are the simplest organic compounds
... For alkanes, the ending is “ane”, giving methane, ethane, propane, etc. Methane is CH4, ethane is C2H6, propane is C3H8 etc. The general formula is CnH2n+2. There are many ways to represent these compounds. For example, butane, C4H10 can be drawn as: or CH3(CH2)2CH3 or simply as ...
... For alkanes, the ending is “ane”, giving methane, ethane, propane, etc. Methane is CH4, ethane is C2H6, propane is C3H8 etc. The general formula is CnH2n+2. There are many ways to represent these compounds. For example, butane, C4H10 can be drawn as: or CH3(CH2)2CH3 or simply as ...
102 Lecture Ch11
... - can bond with other carbons to form chains and rings - can bond with a variety of other elements • Learning organic chemistry will help you understand the nature of the world around you: - pharmaceuticals, household products, plastics, etc. - essential for understanding biology and biochemistry ...
... - can bond with other carbons to form chains and rings - can bond with a variety of other elements • Learning organic chemistry will help you understand the nature of the world around you: - pharmaceuticals, household products, plastics, etc. - essential for understanding biology and biochemistry ...
Alkanes CH4 + Cl2 → CH3Cl + HCl CH3CH3 + Cl2 → CH3CH2Cl +
... Test for halogen atoms in halogeno alkanes, Cl, Br and I Step one - Free the halide ion from the organic molecule. How this is done depends on the type of molecule, but for simple halogeno alkanes it is done by heating the halogenoalkane under reflux with dilute, aqueous sodium hydroxide solution. S ...
... Test for halogen atoms in halogeno alkanes, Cl, Br and I Step one - Free the halide ion from the organic molecule. How this is done depends on the type of molecule, but for simple halogeno alkanes it is done by heating the halogenoalkane under reflux with dilute, aqueous sodium hydroxide solution. S ...
Homework #7, Graded Answers
... e.) 2-methyl-2-pentanol is subjected to oxidation No reaction tertiary alcohols do not oxidize 31.) Each of the following conversions requires more than one step. Show the reagents you would use and draw structural formulas for intermediate compounds formed in each conversion. O ...
... e.) 2-methyl-2-pentanol is subjected to oxidation No reaction tertiary alcohols do not oxidize 31.) Each of the following conversions requires more than one step. Show the reagents you would use and draw structural formulas for intermediate compounds formed in each conversion. O ...
Exam 2 Review A
... You should be familiar with the detailed mechanisms of the SN1 and SN2 reactions. Rate determining steps are important to consider, as are the transition states associated with these steps. Compare and contrast the SN1 and SN2 reactions with respect to kinetics, nature of the electrophile [structure ...
... You should be familiar with the detailed mechanisms of the SN1 and SN2 reactions. Rate determining steps are important to consider, as are the transition states associated with these steps. Compare and contrast the SN1 and SN2 reactions with respect to kinetics, nature of the electrophile [structure ...
orgchem rev integ odd numbers
... Inductive Effect – is an electronic effect due to the polarization of sigma bonds within a molecule or ion. Typically due to an electronegativity difference between the atoms at either end of the bond. ...
... Inductive Effect – is an electronic effect due to the polarization of sigma bonds within a molecule or ion. Typically due to an electronegativity difference between the atoms at either end of the bond. ...
Slides
... Asymmetric synthesis of L-dopa, drug for treating Parkinson’s disease Syn Addition of Hydrogen: Synthesis of cis- Alkenes è The P-2 catalyst nickel boride results in syn addition of one equivalent of hydrogen to a triple bond è An internal alkyne will yield a cis double bond ...
... Asymmetric synthesis of L-dopa, drug for treating Parkinson’s disease Syn Addition of Hydrogen: Synthesis of cis- Alkenes è The P-2 catalyst nickel boride results in syn addition of one equivalent of hydrogen to a triple bond è An internal alkyne will yield a cis double bond ...
Seminar_1 1. Classification and nomenclature of organic
... Whilst many of the alkanes present in crude oil are aliphatic, having straight–or branched–chain molecules, some of them form rings – they are alicyclic. These compounds are denoted as cycloalkanes. These cycloalkanes have the general formula CnH2n instead of CnH2n+2 for the chain molecules. Cycloal ...
... Whilst many of the alkanes present in crude oil are aliphatic, having straight–or branched–chain molecules, some of them form rings – they are alicyclic. These compounds are denoted as cycloalkanes. These cycloalkanes have the general formula CnH2n instead of CnH2n+2 for the chain molecules. Cycloal ...
Ether And Epoxides
... unstable and shock-sensitive due to molecular strain. On standing, they form related peroxidic derivatives, which are also. Due to this, one should never use old bottles of dialkyl ethers, and extreme care must be taken in their uses. ...
... unstable and shock-sensitive due to molecular strain. On standing, they form related peroxidic derivatives, which are also. Due to this, one should never use old bottles of dialkyl ethers, and extreme care must be taken in their uses. ...
Organic Reactions
... • Diatomic gas has two atoms – both add to opposite sides of the double bond (and opposite sides of the ...
... • Diatomic gas has two atoms – both add to opposite sides of the double bond (and opposite sides of the ...
File
... • possibility of isomers being produced. • compared to an alkene, complete addition to an alkyne will require twice the quantity of • halogen (1) • hydrogen (2) • hydrogen halide (3) ...
... • possibility of isomers being produced. • compared to an alkene, complete addition to an alkyne will require twice the quantity of • halogen (1) • hydrogen (2) • hydrogen halide (3) ...
Etherification of monosaccharide with isobutene: A - chem
... The products, depending on the number of substituted OH groups, are expected to have significantly different polarities. Therefore, they should be easily separated by chromatography. Both the reaction mixture and the semi-crude or pure products can be analyzed by HPLC and LC-MS, GC-MS. The project w ...
... The products, depending on the number of substituted OH groups, are expected to have significantly different polarities. Therefore, they should be easily separated by chromatography. Both the reaction mixture and the semi-crude or pure products can be analyzed by HPLC and LC-MS, GC-MS. The project w ...
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.