Handbook for the Lab Course Organic Chemistry I
... Participation in the preliminary talks and seminars is compulsory to pass the course and obtain the certificate. Repeated unexcused absence can result in failing of the course. If you cannot attend a mandatory seminar for a profound reason, please get in touch with Steffen Friedrich (steffen.friedri ...
... Participation in the preliminary talks and seminars is compulsory to pass the course and obtain the certificate. Repeated unexcused absence can result in failing of the course. If you cannot attend a mandatory seminar for a profound reason, please get in touch with Steffen Friedrich (steffen.friedri ...
4. a-Monohalo Ethers in Protection Chemistry
... protection chemistry.[Grenne, 1991] This is partly due to the high reactivity of -halo ethers in nucleophilic displacement reactions, which in many cases assures a complete introduction of the protecting group. Another point of great importance in protection chemistry, is the removal of the protect ...
... protection chemistry.[Grenne, 1991] This is partly due to the high reactivity of -halo ethers in nucleophilic displacement reactions, which in many cases assures a complete introduction of the protecting group. Another point of great importance in protection chemistry, is the removal of the protect ...
Reduction [H]
... Thioacetal (or thioketal) reduction or Mozingo reduction with Raney nickel and hydrogen is a classic method to prepare a methylene group from a carbonyl compound. Raney Nickel was developed in 1926 by American engineer Murray Raney. ( "Method of producing finely-divided nickel,"U.S. patent 1,628,190 ...
... Thioacetal (or thioketal) reduction or Mozingo reduction with Raney nickel and hydrogen is a classic method to prepare a methylene group from a carbonyl compound. Raney Nickel was developed in 1926 by American engineer Murray Raney. ( "Method of producing finely-divided nickel,"U.S. patent 1,628,190 ...
Alkaloids - Angelfire
... They have basic properties, complex structure, physiological active and plant origin is the main characteristic, which define plant alkaloids. Seldom does a single alkaloid occur alone in given plant; rather another accompanies it, which is closely related in structure and biosynthetic origin. The f ...
... They have basic properties, complex structure, physiological active and plant origin is the main characteristic, which define plant alkaloids. Seldom does a single alkaloid occur alone in given plant; rather another accompanies it, which is closely related in structure and biosynthetic origin. The f ...
the beginnings of synthetic organic chemistry: zinc alkyls and the
... as an entity, which passed through chemical transformations unaltered, was established, thanks to the work of Liebig, Wöhler, Bunsen, and Dumas. Then, in 1852, Sir Edward Frankland published the paper in which he proposed that elements have a set saturation capacity— the first proposal of the concep ...
... as an entity, which passed through chemical transformations unaltered, was established, thanks to the work of Liebig, Wöhler, Bunsen, and Dumas. Then, in 1852, Sir Edward Frankland published the paper in which he proposed that elements have a set saturation capacity— the first proposal of the concep ...
EXPERIMENT 9 (Organic Chemistry II) Pahlavan/Cherif
... the compounds have been organized into families, or functional groups, according to common features. Functional groups have characteristic properties and they control the reactivity of the molecule as a whole. Two such functional groups are briefly discussed below. Alcohols represent a class of orga ...
... the compounds have been organized into families, or functional groups, according to common features. Functional groups have characteristic properties and they control the reactivity of the molecule as a whole. Two such functional groups are briefly discussed below. Alcohols represent a class of orga ...
1 -
... Nomenclature of alkynes IUPAC nomenclature (1) Parent name is alkyne i.e. change the -ane to -yne. Choose the longest continuous chain containing the triple bond as the basis for the parent name. The position of the triple bond takes the lowest possible number. If both double and triple ...
... Nomenclature of alkynes IUPAC nomenclature (1) Parent name is alkyne i.e. change the -ane to -yne. Choose the longest continuous chain containing the triple bond as the basis for the parent name. The position of the triple bond takes the lowest possible number. If both double and triple ...
Acid derivatives
... reactions take place. Indeed, an alert reader may well be puzzled by the facility of these nucleophilic substitution reactions. After all, it was previously noted that halogens bonded to sp2 or sp hybridized carbon atoms do not usually undergo substitution reactions with nucleophilic reagents. Furth ...
... reactions take place. Indeed, an alert reader may well be puzzled by the facility of these nucleophilic substitution reactions. After all, it was previously noted that halogens bonded to sp2 or sp hybridized carbon atoms do not usually undergo substitution reactions with nucleophilic reagents. Furth ...
Exam 3 - Napa Valley College
... Why is one more acidic than another? The more acidic alcohol is the smaller alcohol (ie: 1). They have the fewest methyl groups pushing into the OH group. This causes the oxygen to pull as many electrons from the surrounding atoms as possible making the hydrogen more acidic (it leaves easier). As m ...
... Why is one more acidic than another? The more acidic alcohol is the smaller alcohol (ie: 1). They have the fewest methyl groups pushing into the OH group. This causes the oxygen to pull as many electrons from the surrounding atoms as possible making the hydrogen more acidic (it leaves easier). As m ...
Final Study Guide (Semester 2) Answer Key
... 24. Name one commercial item made from petroleum. What petroleum product is used to make it? Basketballs are made from man-made rubber (from petroleum). Go to http://www.adventuresinenergy.org/Oil-and-Natural-Gas-in-Your-Life/index.html for more ideas. Ch. 20 25. How many valence electrons does a ca ...
... 24. Name one commercial item made from petroleum. What petroleum product is used to make it? Basketballs are made from man-made rubber (from petroleum). Go to http://www.adventuresinenergy.org/Oil-and-Natural-Gas-in-Your-Life/index.html for more ideas. Ch. 20 25. How many valence electrons does a ca ...
1 Q. What are Saturated and unsaturated hydrocarbons?imp
... Staggered conformations has the lease torsional strain while eclipsed having maximum. Due to torsional strain, certain energy called torsional energy, is required to allow the rotation around the C-C single bond. in other words ethane molecule having staggered conformation will have to come cross an ...
... Staggered conformations has the lease torsional strain while eclipsed having maximum. Due to torsional strain, certain energy called torsional energy, is required to allow the rotation around the C-C single bond. in other words ethane molecule having staggered conformation will have to come cross an ...
5 organic chemistry: functional groups
... CH2PCH(CH2)3CH3 Br2 88n BrCH2CH(CH2)3CH3 The other crystallizing dish picks up the characteristic color of a dilute solution of bromine because the reagent doesn’t react with alkanes under normal conditions. If the crystallizing dish in the upper right corner is moved into the center of the projec ...
... CH2PCH(CH2)3CH3 Br2 88n BrCH2CH(CH2)3CH3 The other crystallizing dish picks up the characteristic color of a dilute solution of bromine because the reagent doesn’t react with alkanes under normal conditions. If the crystallizing dish in the upper right corner is moved into the center of the projec ...
On the Transition States of Electrophilic Radical Additions to Alkenes
... olefinic carbon atom exert huge ratedecreasing effects.Ib Absolute rate measurements for reactions of tert-butyl radicals with various alkenes exhibit comparable results.' These unequal substituent effects point to unsymmetrical transition states 1 in which only the attacked olefinic carbon atom dev ...
... olefinic carbon atom exert huge ratedecreasing effects.Ib Absolute rate measurements for reactions of tert-butyl radicals with various alkenes exhibit comparable results.' These unequal substituent effects point to unsymmetrical transition states 1 in which only the attacked olefinic carbon atom dev ...
File - Dr KHALID SHADID
... When acyl chlorides react, the leaving group is a chloride ion, and when amides react, the leaving group is an amine (or ammonia). The chloride ions are the weakest bases and acyl chlorides are the must reactive acyl compounds. Amines (or ammonia) are the strongest bases and amides are the least rea ...
... When acyl chlorides react, the leaving group is a chloride ion, and when amides react, the leaving group is an amine (or ammonia). The chloride ions are the weakest bases and acyl chlorides are the must reactive acyl compounds. Amines (or ammonia) are the strongest bases and amides are the least rea ...
Microsoft Word
... CHAPTER 5 Aerobic alcohol oxidation by ruthenium species stabilized on nanocrystalline magnesium oxide by basic ionic liquids. The selective oxidation of alcohols to carbonyl compounds is the foundation of many important industrial and fine-chemical processes. Many stoichiometric oxidants are known ...
... CHAPTER 5 Aerobic alcohol oxidation by ruthenium species stabilized on nanocrystalline magnesium oxide by basic ionic liquids. The selective oxidation of alcohols to carbonyl compounds is the foundation of many important industrial and fine-chemical processes. Many stoichiometric oxidants are known ...
Reactions of Alkenes
... • Activation Energy, Ea: the difference in energy between reactants and the transition state – determines the rate of reaction – if Ea is large, only a few molecular collisions occur with sufficient energy to reach the transition state, and the reaction is slow – if Ea is small, many collisions gene ...
... • Activation Energy, Ea: the difference in energy between reactants and the transition state – determines the rate of reaction – if Ea is large, only a few molecular collisions occur with sufficient energy to reach the transition state, and the reaction is slow – if Ea is small, many collisions gene ...
INORGANIC CHEMISTRY
... (CH3)3PtCl by Pope et al in 1907; bis(cyclopentadiney)iron(II) known as ferrocene, (πC5H5)2Fe, by Wilkinson in 1951. The organometallic compounds such as diethylzinc(II), ferrocene, Zeise salt etc. helped in understanding the formation of chemical bonds. Each element has a definite combining capacit ...
... (CH3)3PtCl by Pope et al in 1907; bis(cyclopentadiney)iron(II) known as ferrocene, (πC5H5)2Fe, by Wilkinson in 1951. The organometallic compounds such as diethylzinc(II), ferrocene, Zeise salt etc. helped in understanding the formation of chemical bonds. Each element has a definite combining capacit ...
Chapter 19. Aldehydes and Ketones: Nucleophilic Addition Reactions
... Aldehydes and ketones are characterized by the carbonyl ...
... Aldehydes and ketones are characterized by the carbonyl ...
REASONING QUESTIONS IN ORGANIC CHEMISTRY TEXT
... Ans: Due to hydrogen bond 27. Explain the fact that in aryl alkyl ethers (i) the alkoxy group activates the benzene ring towards electrophilic substitution and (ii) it directs the incoming substituents to ortho and para positions in benzene ring. Ans: Methoxy group on Benzene ring donates the electr ...
... Ans: Due to hydrogen bond 27. Explain the fact that in aryl alkyl ethers (i) the alkoxy group activates the benzene ring towards electrophilic substitution and (ii) it directs the incoming substituents to ortho and para positions in benzene ring. Ans: Methoxy group on Benzene ring donates the electr ...
REASONING QUESTIONS IN ORGANIC CHEMISTRY
... Ans: Due to hydrogen bond 27. Explain the fact that in aryl alkyl ethers (i) the alkoxy group activates the benzene ring towards electrophilic substitution and (ii) it directs the incoming substituents to ortho and para positions in benzene ring. Ans: Methoxy group on Benzene ring donates the electr ...
... Ans: Due to hydrogen bond 27. Explain the fact that in aryl alkyl ethers (i) the alkoxy group activates the benzene ring towards electrophilic substitution and (ii) it directs the incoming substituents to ortho and para positions in benzene ring. Ans: Methoxy group on Benzene ring donates the electr ...
19.2 preparation of acyl chlorides
... This reaction, known as Fischer esterification, requires the presence of an acid catalyst. Because the carboxylic acid and the ester have similar reactivities, the reaction is useful only if a method can be found to drive the equilibrium in the direction of the desired product—the ester. In accord w ...
... This reaction, known as Fischer esterification, requires the presence of an acid catalyst. Because the carboxylic acid and the ester have similar reactivities, the reaction is useful only if a method can be found to drive the equilibrium in the direction of the desired product—the ester. In accord w ...
Document
... Reaction of “silver mirror” and reaction with Fehling reagent used for identification of aldehyde group. ...
... Reaction of “silver mirror” and reaction with Fehling reagent used for identification of aldehyde group. ...
Şenol, O.İ., Viljava, T.-R., Krause, AOI
... methanol. The water required for the reaction may be supplied by the dehydration of the alcohols in path I. The formed carboxylic acids are either reduced to alcohol releasing a mole of water or decarboxylated to alkenes followed by hydrogenation to the corresponding alkane. Unlike decarboxylation, ...
... methanol. The water required for the reaction may be supplied by the dehydration of the alcohols in path I. The formed carboxylic acids are either reduced to alcohol releasing a mole of water or decarboxylated to alkenes followed by hydrogenation to the corresponding alkane. Unlike decarboxylation, ...
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.