Preparation of Aldehydes and Ketones
... NaBH4 and LiAlH4 reduce carbonyl groups but not carbon-carbon double bonds: ...
... NaBH4 and LiAlH4 reduce carbonyl groups but not carbon-carbon double bonds: ...
Catalysis Web Pages for Pre-University
... The manufacture of sulfuric acid The traditional example of catalysis in the manufacture of another of the world’s bulk chemicals is the Contact process for the manufacture of sulfuric acid. It used to be said that one measure of a country’s wealth was its output of sulfuric acid. In the three step ...
... The manufacture of sulfuric acid The traditional example of catalysis in the manufacture of another of the world’s bulk chemicals is the Contact process for the manufacture of sulfuric acid. It used to be said that one measure of a country’s wealth was its output of sulfuric acid. In the three step ...
V a.) \
... becomea cation is called aprotonated amine. Thecations produced by protonation of aliphatic and aromatic amines are calledallcylammonium ions and arylarnmonium ions, respectiuely.An electrically neutral, unprotonated amine is called afueeamine. Amines are bases,so they can reactwith acidsto form sal ...
... becomea cation is called aprotonated amine. Thecations produced by protonation of aliphatic and aromatic amines are calledallcylammonium ions and arylarnmonium ions, respectiuely.An electrically neutral, unprotonated amine is called afueeamine. Amines are bases,so they can reactwith acidsto form sal ...
Synthesis of Benzyl Acetate from Acetic Anhydride
... To a reaction tube add 540 mg of benzyl alcohol and 510 mg of acetic anhydride and a boiling chip. Attach the empty distilling column as an air condenser. Reflux the resulting mixture for 1 h or more, then cool it to room temperature. Add 1 mL of ether (use the wet ether found in a supply bottle in ...
... To a reaction tube add 540 mg of benzyl alcohol and 510 mg of acetic anhydride and a boiling chip. Attach the empty distilling column as an air condenser. Reflux the resulting mixture for 1 h or more, then cool it to room temperature. Add 1 mL of ether (use the wet ether found in a supply bottle in ...
Experiments
... Forms H-Bonds with water, but lower solubility than ethanol due to the arene ring. Formerly known as carbolic acid, the pH is only just less than 7 in water. The reason phenols are acidic and alcohols aren’t is because the lone pairs, in their interaction with the delocalised benzene ring, stabilise ...
... Forms H-Bonds with water, but lower solubility than ethanol due to the arene ring. Formerly known as carbolic acid, the pH is only just less than 7 in water. The reason phenols are acidic and alcohols aren’t is because the lone pairs, in their interaction with the delocalised benzene ring, stabilise ...
Alcohols, Phenols, Thiols, and Ethers
... • The characteristic functional group of alcohols and phenols is the hydroxyl group (-OH). • Alcohols have the general structure R-OH, in which R is any alkyl group. • Phenols have the general structure R-OH, in which R is an aryl group. • They are substituted water molecules in which one of the hyd ...
... • The characteristic functional group of alcohols and phenols is the hydroxyl group (-OH). • Alcohols have the general structure R-OH, in which R is any alkyl group. • Phenols have the general structure R-OH, in which R is an aryl group. • They are substituted water molecules in which one of the hyd ...
Chapter 2. CLASSIFICATION AND NOMENCLATURE OF ORGANIC
... There are two types of characteristic groups. One type is designated in a name only as prefixes. Nitro group, halogens, and some other groups belong to this type; they are listed in the lower part of Table 2.2. Most of characteristic groups (the upper part of Table 2.2, beyond the coloured line) may ...
... There are two types of characteristic groups. One type is designated in a name only as prefixes. Nitro group, halogens, and some other groups belong to this type; they are listed in the lower part of Table 2.2. Most of characteristic groups (the upper part of Table 2.2, beyond the coloured line) may ...
The Chemistry of Life: Organic Compounds
... Functional groups change the properties of organic molecules The existence of isomers is not the only source of variety among organic molecules. The addition of various combinations of atoms generates a vast array of molecules with different properties. Because covalent bonds between hydrogen and ca ...
... Functional groups change the properties of organic molecules The existence of isomers is not the only source of variety among organic molecules. The addition of various combinations of atoms generates a vast array of molecules with different properties. Because covalent bonds between hydrogen and ca ...
Question paper
... A adding dilute sulfuric acid to lead metal. B adding concentrated sulfuric acid to lead metal. C adding dilute sulfuric acid to lead(II) nitrate solution. D adding dilute sulfuric acid to solid lead(II) oxide. (Total for Question 11 = 1 mark) ...
... A adding dilute sulfuric acid to lead metal. B adding concentrated sulfuric acid to lead metal. C adding dilute sulfuric acid to lead(II) nitrate solution. D adding dilute sulfuric acid to solid lead(II) oxide. (Total for Question 11 = 1 mark) ...
The Core Principles of Chemistry
... A adding dilute sulfuric acid to lead metal. B adding concentrated sulfuric acid to lead metal. C adding dilute sulfuric acid to lead(II) nitrate solution. D adding dilute sulfuric acid to solid lead(II) oxide. (Total for Question 11 = 1 mark) ...
... A adding dilute sulfuric acid to lead metal. B adding concentrated sulfuric acid to lead metal. C adding dilute sulfuric acid to lead(II) nitrate solution. D adding dilute sulfuric acid to solid lead(II) oxide. (Total for Question 11 = 1 mark) ...
Amines are compounds characterized by the presence of
... Due to the lone pair of electrons, amines are basiccompounds. The basicity of the compound can be influenced by neighboring atoms, steric bulk, and the solubility of the corresponding cation to be formed. Amine compounds can hydrogen bond, which affords them solubility in water and elevated boiling ...
... Due to the lone pair of electrons, amines are basiccompounds. The basicity of the compound can be influenced by neighboring atoms, steric bulk, and the solubility of the corresponding cation to be formed. Amine compounds can hydrogen bond, which affords them solubility in water and elevated boiling ...
Chap5
... If these effluents contain nutrients (N, K, P) which are often limited in the natural environment, it can lead to eutrophication. BOD: (biological oxygen demand) the capacity of the organic matter in a sample of natural water to consume oxygen. The BOD should be much lower than 8.7 mgO2/L (O2 satura ...
... If these effluents contain nutrients (N, K, P) which are often limited in the natural environment, it can lead to eutrophication. BOD: (biological oxygen demand) the capacity of the organic matter in a sample of natural water to consume oxygen. The BOD should be much lower than 8.7 mgO2/L (O2 satura ...
9: Formation of Alkenes and Alkynes. Elimination Reactions
... This carbanion then loses the leaving group (-:L) to form alkene product(s). The E1cb mechanism usually occurs with strong bases and with substrates where groups directly attached to the carbanion center can stabilize the negative charge on that carbanion center. We have not yet introduced most grou ...
... This carbanion then loses the leaving group (-:L) to form alkene product(s). The E1cb mechanism usually occurs with strong bases and with substrates where groups directly attached to the carbanion center can stabilize the negative charge on that carbanion center. We have not yet introduced most grou ...
1.4 Alcohols, Ethers, and Thiols
... • A primary alcohol is an alcohol in which the hydroxyl group is bonded to a terminal carbon atom • A secondary alcohol is an alcohol in which the hydroxyl group is bonded to a carbon atom with two alkyl groups bonded to it • A tertiary alcohol is an alcohol in which the hydroxyl group is bonded to ...
... • A primary alcohol is an alcohol in which the hydroxyl group is bonded to a terminal carbon atom • A secondary alcohol is an alcohol in which the hydroxyl group is bonded to a carbon atom with two alkyl groups bonded to it • A tertiary alcohol is an alcohol in which the hydroxyl group is bonded to ...
Aldehydes and ketones
... You are given three liquids which are not labelled. However you know that one of them is an alcohol, one of them is an aldehyde and one of them is a ketone. Describe how you would identify them, using chemical tests. ...
... You are given three liquids which are not labelled. However you know that one of them is an alcohol, one of them is an aldehyde and one of them is a ketone. Describe how you would identify them, using chemical tests. ...
Oxidation of Cyclohexanol to Cyclohexanone Notes
... Cyclohexanol is an irritant. Avoid contact with skin, eyes, and clothing. Glacial acetic acid is a dehydrating agent, an irritant, and corrosive which means it causes burns. Handle it with care. Dispense it in a fume hood and avoid contact with skin, eyes, and clothing. Sodium hypochlorite solution ...
... Cyclohexanol is an irritant. Avoid contact with skin, eyes, and clothing. Glacial acetic acid is a dehydrating agent, an irritant, and corrosive which means it causes burns. Handle it with care. Dispense it in a fume hood and avoid contact with skin, eyes, and clothing. Sodium hypochlorite solution ...
15_01_05.html
... Isopropyl alcohol is prepared by hydration of propene. All alcohols with four carbons or fewer are readily available. Most alcohols with five or six carbons are readily available. ...
... Isopropyl alcohol is prepared by hydration of propene. All alcohols with four carbons or fewer are readily available. Most alcohols with five or six carbons are readily available. ...
Chapter 4 Study Guide
... cyclodecane and cyclooctane come next in ring strain. cyclopentane and heptane have very little ring strain cyclopentadecane and cyclohexane have almost no ring strain 3. angle strain makes up most of ring strain due to angles being less than the tetrahedral angles that are preferred cyclopropane is ...
... cyclodecane and cyclooctane come next in ring strain. cyclopentane and heptane have very little ring strain cyclopentadecane and cyclohexane have almost no ring strain 3. angle strain makes up most of ring strain due to angles being less than the tetrahedral angles that are preferred cyclopropane is ...
Alkyl halide
... • Reaction of (R)-6-chloro-2,6-dimethyloctane with H2O • Product is approximately 80% racemized and 20% inverted (80% R,S + 20% S is equivalent to 40% R and 60% S). ...
... • Reaction of (R)-6-chloro-2,6-dimethyloctane with H2O • Product is approximately 80% racemized and 20% inverted (80% R,S + 20% S is equivalent to 40% R and 60% S). ...
Lecture (8)
... Hydrocarbons derivatives: The vast majority of organic molecules contain elements in addition to carbon and hydrogen. However, most of these substances can be viewed as hydrocarbons derivatives; e.g.: alcohols and phenols, aldehydes and ketons and carboxylic acids. ...
... Hydrocarbons derivatives: The vast majority of organic molecules contain elements in addition to carbon and hydrogen. However, most of these substances can be viewed as hydrocarbons derivatives; e.g.: alcohols and phenols, aldehydes and ketons and carboxylic acids. ...
Carboxylic Acid Questions 1.-Arrange the following in order of (i
... The aldehyde and ketone will undergo nucleophilic addition, the acid and the ester nucleophilic acyl substitution. Consider the electrophilicity of the carbonyl group in each compound in each ...
... The aldehyde and ketone will undergo nucleophilic addition, the acid and the ester nucleophilic acyl substitution. Consider the electrophilicity of the carbonyl group in each compound in each ...
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.