Current Research Click Here
... the decrease in concentration using the mini GC. For additional information: http://www.vernier.com/products/sensors/gc2-mini/ . Two videos are also available for viewing so you can see the importance of this technique in organic chemistry. The only limitation to using the mini GC is the boiling poi ...
... the decrease in concentration using the mini GC. For additional information: http://www.vernier.com/products/sensors/gc2-mini/ . Two videos are also available for viewing so you can see the importance of this technique in organic chemistry. The only limitation to using the mini GC is the boiling poi ...
nomenclature continued… - Turner Fenton Secondary School
... hydroxyl group on terminal carbon. COOH group is always found on the terminal carbon. Many common names for various substances: Formic acid and acetic acid. ...
... hydroxyl group on terminal carbon. COOH group is always found on the terminal carbon. Many common names for various substances: Formic acid and acetic acid. ...
Unit 3 Organic Chemistry - Corner Brook Regional High
... The huge number of organic compounds is due mainly to the ability of carbon atoms to form stable chains, branched chains, rings, branched rings, multiple rings, and multiple bonds (double and triple bonds) to itself and to many other non-metal atoms. ...
... The huge number of organic compounds is due mainly to the ability of carbon atoms to form stable chains, branched chains, rings, branched rings, multiple rings, and multiple bonds (double and triple bonds) to itself and to many other non-metal atoms. ...
chemistry (paper 2)
... Functional series → double or triple bonds are functional groups. They are ‘add-ons’ that change the chemistry of a carbon chain ...
... Functional series → double or triple bonds are functional groups. They are ‘add-ons’ that change the chemistry of a carbon chain ...
S3 Summary - Glow Blogs
... -CH3 methyl -CH2CH3 ethyl -if more than one of same branch use prefix di ( if two ) tri ( if three ) - name branched alkane 2,3-dimethylhexane Naming Branched Alkenes ...
... -CH3 methyl -CH2CH3 ethyl -if more than one of same branch use prefix di ( if two ) tri ( if three ) - name branched alkane 2,3-dimethylhexane Naming Branched Alkenes ...
1-1 EXPERIMENT 1: Preparation and Reactivity of Alkyl Halides
... one-step, concerted, SN2 reaction. Therefore, the reaction occurs most quickly when attack at the carbon that bears the halogen (X) is least hindered sterically. For alkyl halides, the order of reactivity is primary > secondary > tertiary. (ii) Lucas Test: Test for SN1 The reactivity of the product ...
... one-step, concerted, SN2 reaction. Therefore, the reaction occurs most quickly when attack at the carbon that bears the halogen (X) is least hindered sterically. For alkyl halides, the order of reactivity is primary > secondary > tertiary. (ii) Lucas Test: Test for SN1 The reactivity of the product ...
Chapter 6: Molecular Modeling Problems
... Molecular Modeling Problems lengths for ethane (1.531Ǻ), propane (1.526Ǻ), 2-methylpropane (1.541Ǻ) and 3,3-dimethylpropane (1.540Ǻ) show only slight variation. Is this always the case? Obtain carbon-fluorine bond lengths in fluoromethanes, CFnH4-n (n=1-4). Do they increase or decrease significantl ...
... Molecular Modeling Problems lengths for ethane (1.531Ǻ), propane (1.526Ǻ), 2-methylpropane (1.541Ǻ) and 3,3-dimethylpropane (1.540Ǻ) show only slight variation. Is this always the case? Obtain carbon-fluorine bond lengths in fluoromethanes, CFnH4-n (n=1-4). Do they increase or decrease significantl ...
Quarter 3: Post Test Review
... 44. ________ mmHg = __________torr = _________Pascals = __________kilopascals Convert 2983.4 mmHg into torr. ___________________ convert in Pascals ________________ E. Bonding and Electron Configurations 45. Besides metallic, what are the other two types of bonding. _____________ and __________ b. d ...
... 44. ________ mmHg = __________torr = _________Pascals = __________kilopascals Convert 2983.4 mmHg into torr. ___________________ convert in Pascals ________________ E. Bonding and Electron Configurations 45. Besides metallic, what are the other two types of bonding. _____________ and __________ b. d ...
Level 3 Distinguishing between organic substances
... • include reagents used, and • link the observed results to the reactions occurring at the functional groups present in the organic ...
... • include reagents used, and • link the observed results to the reactions occurring at the functional groups present in the organic ...
CAPE CHEMISTRY UNIT II MODULE I Alkanes and Alkenes
... ethyl hydrogensulphate + ethanol (excess) Diethyl ether (ethoxyethane) + sulphuric acid If the concentrated sulphuric is in excess and the temperature is raised to 170oC, water is eliminated, with the formation of an alkene: ethyl hydrogensulphate + conc. sulphuric acid (excess) ethene + sulphur ...
... ethyl hydrogensulphate + ethanol (excess) Diethyl ether (ethoxyethane) + sulphuric acid If the concentrated sulphuric is in excess and the temperature is raised to 170oC, water is eliminated, with the formation of an alkene: ethyl hydrogensulphate + conc. sulphuric acid (excess) ethene + sulphur ...
CHEMISTRY
... (4) Alumina 3. Nichrome used as heating element in hot-air oven is an alloy of: (1) Ni and Cr (2) Ni and Fe (3) Fe and Cr (4) Ni, Fe and Cr 4. The indicator used to detect the end point in the titration of a weak acid and strong base (pH-8-10) is: ...
... (4) Alumina 3. Nichrome used as heating element in hot-air oven is an alloy of: (1) Ni and Cr (2) Ni and Fe (3) Fe and Cr (4) Ni, Fe and Cr 4. The indicator used to detect the end point in the titration of a weak acid and strong base (pH-8-10) is: ...
CAN YOU …
... *** This is in no way meant to be an exam outline or a complete review of all the topics covered • identify an organic compound • distinguish between saturated and unsaturated ...
... *** This is in no way meant to be an exam outline or a complete review of all the topics covered • identify an organic compound • distinguish between saturated and unsaturated ...
Lab Activity: Functional Groups
... 4. Write down the structural equation for this reaction, name the products(s) and identify the type of reaction. ...
... 4. Write down the structural equation for this reaction, name the products(s) and identify the type of reaction. ...
Organic Chemistry (HL) Revision Questions
... 2-chloro-3-methylbutane reacts with sodium hydroxide via an SN2 mechanism. Explain the mechanism by using curly arrows to represent the movement of electron pairs. ...
... 2-chloro-3-methylbutane reacts with sodium hydroxide via an SN2 mechanism. Explain the mechanism by using curly arrows to represent the movement of electron pairs. ...
DESIGN OF CHIRAL IMINO- AND AMINOPYRIDINE LIGANDS
... The synthesis of new molecules that can work as chiral ligands in metal catalyzed enantioselective reactions is currently an area of great interest.1,2 These ligands must be capable of coordinating with the metal ion, generating around it a highly asymmetric environment so that the complex formed is ...
... The synthesis of new molecules that can work as chiral ligands in metal catalyzed enantioselective reactions is currently an area of great interest.1,2 These ligands must be capable of coordinating with the metal ion, generating around it a highly asymmetric environment so that the complex formed is ...
Answer Key to Assignment #7
... 2. How would you prepare the following molecules? More than one step may be necessary. You may use any reagents/solvents you wish. ...
... 2. How would you prepare the following molecules? More than one step may be necessary. You may use any reagents/solvents you wish. ...
Combinatorial chemistry
... What is it about? • Synthesising a large number of similar compounds in a short period of time. • Compounds that are generated are analogues of compounds that are already biologically active • Chemists want to find a new medicine that is more effective than an existing one, or causes fewer side eff ...
... What is it about? • Synthesising a large number of similar compounds in a short period of time. • Compounds that are generated are analogues of compounds that are already biologically active • Chemists want to find a new medicine that is more effective than an existing one, or causes fewer side eff ...
Notes on Substitutions and Eliminations
... on the neighboring carbon, and that the leaving group and eliminated H are 180° apart from each other (anti-periplanar). 2. The leaving group – like the SN2 reaction, this does not rely on an exceptional leaving group. 3. The base – A strong base is needed to start the reaction. This can be accompli ...
... on the neighboring carbon, and that the leaving group and eliminated H are 180° apart from each other (anti-periplanar). 2. The leaving group – like the SN2 reaction, this does not rely on an exceptional leaving group. 3. The base – A strong base is needed to start the reaction. This can be accompli ...
L3 - Alcohol and Phenol Reactions
... For reaction that yield multiple possible products, the major product is predicted using Saytzeff’s Rule ...
... For reaction that yield multiple possible products, the major product is predicted using Saytzeff’s Rule ...
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.