Chapter 8
... Basicity of Amines • Aliphatic amines have about the same base strength, and are slightly stronger bases than NH3. • Aromatic and heterocyclic aromatic. • amines are considerably weaker bases than aliphatic amines. • Note that while aliphatic amines are weak bases by comparison with inorganic bases ...
... Basicity of Amines • Aliphatic amines have about the same base strength, and are slightly stronger bases than NH3. • Aromatic and heterocyclic aromatic. • amines are considerably weaker bases than aliphatic amines. • Note that while aliphatic amines are weak bases by comparison with inorganic bases ...
Exam 2 Review A
... 1. Be able to explain the physical basis of NMR spectroscopy in terms of spins, energy levels, a magnetic field, and radiowaves. 2. Be able to explain the origin of factors affecting the chemical shift, such as diamagnetic shielding, electronegativity, and ring current effects. 3. Be able to use the ...
... 1. Be able to explain the physical basis of NMR spectroscopy in terms of spins, energy levels, a magnetic field, and radiowaves. 2. Be able to explain the origin of factors affecting the chemical shift, such as diamagnetic shielding, electronegativity, and ring current effects. 3. Be able to use the ...
Carboxylic Acid Derivatives and Nucleophilic Acyl Substitution
... • Reaction with thionyl chloride, SOCl2 ...
... • Reaction with thionyl chloride, SOCl2 ...
New process of low-temperature methanol synthesis from CO/CO2
... It is well known that for methanol synthesis from CO/CO2/H2 over supported copper-based catalysts formate was the key intermediate, which was further hydrogenated to produce methanol[3]. The hydrogenolysis of formate has two ways: direct hydrogenolysis and indirect one. In the former, HCOO was hydro ...
... It is well known that for methanol synthesis from CO/CO2/H2 over supported copper-based catalysts formate was the key intermediate, which was further hydrogenated to produce methanol[3]. The hydrogenolysis of formate has two ways: direct hydrogenolysis and indirect one. In the former, HCOO was hydro ...
Ruthenium And Silver Reagents
... Ruthenium Reagents Ruthenium Tetroxide - effective for the conversion of 1° alcohols to RCO2H and 2° alcohols to ketones - oxidizes multiple bonds and 1,2-diols. ...
... Ruthenium Reagents Ruthenium Tetroxide - effective for the conversion of 1° alcohols to RCO2H and 2° alcohols to ketones - oxidizes multiple bonds and 1,2-diols. ...
ch16 by dr. Dina
... Dissolving aldehydes (or ketones) in water causes formation of an equilibrium between the carbonyl compound and its hydrate The hydrate is also called a gem-diol (gem i.e. geminal, indicates the presence of two identical substituents on the same carbon) The equilibrum favors a ketone over its hyd ...
... Dissolving aldehydes (or ketones) in water causes formation of an equilibrium between the carbonyl compound and its hydrate The hydrate is also called a gem-diol (gem i.e. geminal, indicates the presence of two identical substituents on the same carbon) The equilibrum favors a ketone over its hyd ...
Test1-W09-C12-13
... carbon atoms are compared, it is always found that the cycloalkane has A) two more hydrogen atoms. B) the same number of hydrogen atoms. C) two less hydrogen atoms. D) four less hydrogen atoms. ...
... carbon atoms are compared, it is always found that the cycloalkane has A) two more hydrogen atoms. B) the same number of hydrogen atoms. C) two less hydrogen atoms. D) four less hydrogen atoms. ...
121. Acceptorless Dehydrogenation with Metal
... Efficiency of the Metal-ligand Cooperation catalysts are quite high. Catalysts load can be as high as 0.1%. Scope of the substrates are quite large. Aryl, alkyl, alkeyl(some examples) are both appropriate substituent groups of the substrates. Detailed studied about the operation pattern of cat ...
... Efficiency of the Metal-ligand Cooperation catalysts are quite high. Catalysts load can be as high as 0.1%. Scope of the substrates are quite large. Aryl, alkyl, alkeyl(some examples) are both appropriate substituent groups of the substrates. Detailed studied about the operation pattern of cat ...
Introduction to Alkyl Halides, Alcohols, Ethers, Thiols
... (a) Only the alcohol, 2-methylcyclohexanol, will react with sodium hydride to give a gaseous product (H2). (b) The alcohol 2-(methylthio)ethanol, CH3SCH2CH2OH, because of its considerably greater ability to serve as both a hydrogen-bond acceptor and a hydrogen-bond donor, is the water-soluble compou ...
... (a) Only the alcohol, 2-methylcyclohexanol, will react with sodium hydride to give a gaseous product (H2). (b) The alcohol 2-(methylthio)ethanol, CH3SCH2CH2OH, because of its considerably greater ability to serve as both a hydrogen-bond acceptor and a hydrogen-bond donor, is the water-soluble compou ...
CH 18 blackboard
... Simple aldehydes are systematically named according to the number of carbon atoms in the longest continuous carbon chain that contains the carbonyl group. The base name is formed by dropping the -e and adding the ending -al. Simple ketones are systematically named according to the longest continuous ...
... Simple aldehydes are systematically named according to the number of carbon atoms in the longest continuous carbon chain that contains the carbonyl group. The base name is formed by dropping the -e and adding the ending -al. Simple ketones are systematically named according to the longest continuous ...
asymmetric alkyne addition to aldehydes
... Chiral propargylic alcohols are important compounds, as this structural motif is often found in pharmaceutical compounds as well as natural products and can also serve as versatile synthetic intermediates.1 Although there are many methods available for the preparation of these compounds (e.g. asymme ...
... Chiral propargylic alcohols are important compounds, as this structural motif is often found in pharmaceutical compounds as well as natural products and can also serve as versatile synthetic intermediates.1 Although there are many methods available for the preparation of these compounds (e.g. asymme ...
m4 carbonyl
... 2,4-DINITROPHENYLHYDRAZINE C6H3(NO2)2NHNH2 The following structural isomers have similar boiling points because of similar van der Waals forces and dipole-dipole interactions. They would be impossible to identify with any precision using boiling point determination. ...
... 2,4-DINITROPHENYLHYDRAZINE C6H3(NO2)2NHNH2 The following structural isomers have similar boiling points because of similar van der Waals forces and dipole-dipole interactions. They would be impossible to identify with any precision using boiling point determination. ...
The presence of an aromatic ring or other
... more than 5 minutes because oxidation of the alcohol will begin slowly. Record your observations. Perform this test on cyclohexene, toluene, and your unknown. Ignition Test The presence of an aromatic ring or other centers of unsaturation will lead to the production of a sooty yellow flame in this t ...
... more than 5 minutes because oxidation of the alcohol will begin slowly. Record your observations. Perform this test on cyclohexene, toluene, and your unknown. Ignition Test The presence of an aromatic ring or other centers of unsaturation will lead to the production of a sooty yellow flame in this t ...
Carboxylic Acids - University of Nebraska Omaha
... Reaction with Bases • Carboxylic acids, whether soluble or insoluble in water, react with NaOH, KOH, and other strong bases to give water-soluble salts. ...
... Reaction with Bases • Carboxylic acids, whether soluble or insoluble in water, react with NaOH, KOH, and other strong bases to give water-soluble salts. ...
Reactions of Alkyl Halides (SN1, SN2, E1, and E2 reactions)
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
Reactions of Alkyl Halides (SN1, SN2, E1, and E2 reactions)
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
Alkyl Halides SN and E reactions
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
... 3. Consider the nature of the solvent: For SN1 reactions, the solvent affects the rate only if it influences the stability of the charged transition state, i.e., the C+. The Nu:- is not involved in the rate determining step so solvent effects on the Nu:- do not affect the rate of SN1 reactions. ...
Page 1 - WordPress.com
... Suggest an alternative name for the term acidity regulator. Explain how a mixture of lactic acid and sodium lactate can act as a regulator when natural processes increase the acidity in some foods. (3) ...
... Suggest an alternative name for the term acidity regulator. Explain how a mixture of lactic acid and sodium lactate can act as a regulator when natural processes increase the acidity in some foods. (3) ...
The presence of an aromatic ring or other
... Procedure: Dissolve 2 drops of a liquid or 25 mg of a solid compound (known or unknown) in 2 mL of water or ethanol. Slowly add 10-20 drops of the potassium permanganate solution drop-wise while shaking. In a positive test, the purple color of the reagent is discharged, and a brown precipitate of ma ...
... Procedure: Dissolve 2 drops of a liquid or 25 mg of a solid compound (known or unknown) in 2 mL of water or ethanol. Slowly add 10-20 drops of the potassium permanganate solution drop-wise while shaking. In a positive test, the purple color of the reagent is discharged, and a brown precipitate of ma ...
7. Organic halides
... opening (see p. 20) instead of substitution characteristic of alkanes. The reactivity of small rings results from their abnormal bond angle (Baeyer strain theory). In cyclopropane the internal bond angle must be 60° (less by 49.5° than the normal tetrahedral bond angle of an sp3-hybridized carbon at ...
... opening (see p. 20) instead of substitution characteristic of alkanes. The reactivity of small rings results from their abnormal bond angle (Baeyer strain theory). In cyclopropane the internal bond angle must be 60° (less by 49.5° than the normal tetrahedral bond angle of an sp3-hybridized carbon at ...
3.8 Aldehydes and ketones
... a) CH3CHO b) CH3COCH3 c) CH3CH2CH2CHO d) CH3CH2CHO 5) a) Draw the structure of 2 – hydroxy propanitrile: ...
... a) CH3CHO b) CH3COCH3 c) CH3CH2CH2CHO d) CH3CH2CHO 5) a) Draw the structure of 2 – hydroxy propanitrile: ...
An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol1
... a sodium hypochlorite (bleach) solution3 through the top of the air condenser over a period of about 35 minutes. When the addition is complete, stir the mixture for an additional 15 minutes. Extraction of Camphor. When the reaction time is complete, allow the mixture to cool to room temperature. Rem ...
... a sodium hypochlorite (bleach) solution3 through the top of the air condenser over a period of about 35 minutes. When the addition is complete, stir the mixture for an additional 15 minutes. Extraction of Camphor. When the reaction time is complete, allow the mixture to cool to room temperature. Rem ...
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.