Topic 10: Organic Chemistry P1: …….. / 15p. P2: ……. / 29p.
... The correct IUPAC name of the molecule is 2-methylpentane. All the bond angles will be approximately 90°. One isomer of this molecule is pentane. The boiling point of this compound would be higher than that of pentane. ...
... The correct IUPAC name of the molecule is 2-methylpentane. All the bond angles will be approximately 90°. One isomer of this molecule is pentane. The boiling point of this compound would be higher than that of pentane. ...
Chapter 10
... We have observed previously that especially with charged species, structures that can resonate the charge onto multiple atoms are more stable than compounds that isolate the charge on a single atom ...
... We have observed previously that especially with charged species, structures that can resonate the charge onto multiple atoms are more stable than compounds that isolate the charge on a single atom ...
Aldehydes and Ketones
... A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
... A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
Aldehydes and Ketones
... A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
... A phosphorus ylide adds to an aldehyde or ketone to yield a dipolar intermediate called a betaine The intermediate spontaneously decomposes through a four-membered ring to yield alkene and triphenylphosphine oxide, (Ph)3P=O ...
Synthesis Explorer
... the three-membered ring of epoxyethane which is then hydrolysed with water or dilute acid to form ethane-1,2-diol. ...
... the three-membered ring of epoxyethane which is then hydrolysed with water or dilute acid to form ethane-1,2-diol. ...
Aldehydes and Ketones
... alkylbenzenes, but it also works with other ketones or aldehydes that are not sensitive to acid. The carbonyl compound is heated with an excess of amalgamated zinc (zinc treated with mercury; Zn (Hg), and concentrated hydrochloric acid (HCl). The actual reduction occurs by a complex mechanism on the ...
... alkylbenzenes, but it also works with other ketones or aldehydes that are not sensitive to acid. The carbonyl compound is heated with an excess of amalgamated zinc (zinc treated with mercury; Zn (Hg), and concentrated hydrochloric acid (HCl). The actual reduction occurs by a complex mechanism on the ...
5 Alkenes and Alkynes GOB Structures
... • is an important plant hormone involved in promoting the ripening of fruits such as bananas. • accelerates the breakdown of cellulose in plants, which causes flowers to wilt and leaves to fall from trees. General, Organic, and Biological Chemistry: Structures of Life, 5/e Karen C. Timberlake ...
... • is an important plant hormone involved in promoting the ripening of fruits such as bananas. • accelerates the breakdown of cellulose in plants, which causes flowers to wilt and leaves to fall from trees. General, Organic, and Biological Chemistry: Structures of Life, 5/e Karen C. Timberlake ...
Nitrogen Compounds
... The conditions are below 10◦C and remember the HNO2 (nitrous acid) is prepared in situ by reacting sodium nitrite with hydrochloric acid. The diazonium salt can then do one of two things depending on the temperature ...
... The conditions are below 10◦C and remember the HNO2 (nitrous acid) is prepared in situ by reacting sodium nitrite with hydrochloric acid. The diazonium salt can then do one of two things depending on the temperature ...
CARBON AND ITS COMPOUNDS
... When three pairs of electrons are shared between two combining atoms, a triple bond is formed. In a triple bond each element shares three electrons. A triple bond is denoted by triple dash ( ≡ ) e.g. N 2 , C 2 H 2 . Formation of N2 molecule Nitrogen has the atomic number 7. It has five electrons in ...
... When three pairs of electrons are shared between two combining atoms, a triple bond is formed. In a triple bond each element shares three electrons. A triple bond is denoted by triple dash ( ≡ ) e.g. N 2 , C 2 H 2 . Formation of N2 molecule Nitrogen has the atomic number 7. It has five electrons in ...
Unit 2 Summary - A
... (n) carry out calculations to determine the atom economy of a reaction; Calculate the atom economy of the following different ways of preparing ethanol: the hydrolysis of bromoethane: C2H5Br + NaOH C2H5OH + NaBr the fermentation of glucose: C6H12O6 2C2H5OH + 2CO2 the hydration of ethane: C2H4 + ...
... (n) carry out calculations to determine the atom economy of a reaction; Calculate the atom economy of the following different ways of preparing ethanol: the hydrolysis of bromoethane: C2H5Br + NaOH C2H5OH + NaBr the fermentation of glucose: C6H12O6 2C2H5OH + 2CO2 the hydration of ethane: C2H4 + ...
Reaction with hydrogen halides
... The main features of a homologous series are: successive members of a homologous series differ by a –CH2- group, can be represented by the same general formula, show a gradation in their physical properties, have similar chemical properties Structural isomers are molecules that have the same molecul ...
... The main features of a homologous series are: successive members of a homologous series differ by a –CH2- group, can be represented by the same general formula, show a gradation in their physical properties, have similar chemical properties Structural isomers are molecules that have the same molecul ...
CHEMISTRY 1000
... group (the carbonyl) and left others alone (e.g. alkenes). If we want to reduce an alkene or alkyne, we need to use a different kind of hydrogen source – one which is not chemoselective but will add hydrogen across any bond. We want our hydrogen source to be, quite literally, hydrogen (H2). Proble ...
... group (the carbonyl) and left others alone (e.g. alkenes). If we want to reduce an alkene or alkyne, we need to use a different kind of hydrogen source – one which is not chemoselective but will add hydrogen across any bond. We want our hydrogen source to be, quite literally, hydrogen (H2). Proble ...
Chapter 19 - people.vcu.edu
... nitrogen, changing them from R to S. There are two times when chirality is locked. Quaternary ammonium salts Sometimes sterics can prevent the lone pair from flipping. Physical properties o Strongly polar o Can hydrogen-bond if they are 1° or 2° Remember that the hydrogen bonding of nitrogen ...
... nitrogen, changing them from R to S. There are two times when chirality is locked. Quaternary ammonium salts Sometimes sterics can prevent the lone pair from flipping. Physical properties o Strongly polar o Can hydrogen-bond if they are 1° or 2° Remember that the hydrogen bonding of nitrogen ...
6.5. alcohols
... This reaction with PCl5 (phosphorous(v)chloride) can be used as a test for alcohols. You would observe misty fumes of HCl produced. ...
... This reaction with PCl5 (phosphorous(v)chloride) can be used as a test for alcohols. You would observe misty fumes of HCl produced. ...
ppt
... 2. CO32– -promoted C–H carboxylation 3. CO2 utilization cycle 4. CO2 as a feedstock for synthesis of FDCA ...
... 2. CO32– -promoted C–H carboxylation 3. CO2 utilization cycle 4. CO2 as a feedstock for synthesis of FDCA ...
Unit 5 - Organic Chemistry 2 student notes
... Solubility of alcohols in water The small alcohols are completely soluble in water. Whatever proportions you mix them in, you will get a single solution. However, solubility falls as the length of the hydrocarbon chain in the alcohol increases. Once you get to four carbons and beyond, the fall in so ...
... Solubility of alcohols in water The small alcohols are completely soluble in water. Whatever proportions you mix them in, you will get a single solution. However, solubility falls as the length of the hydrocarbon chain in the alcohol increases. Once you get to four carbons and beyond, the fall in so ...
Document
... A. Oxidation of tert-butanol with potassium dichromate, in the presence of sulphuric acid, leads to butanoic acid. B. When alcohols are oxidized with potassium permanganate, in the presence of sulphuric acid, the colour of the reaction mixture turns form orange to green. C. 2-ketopentanoic acid and ...
... A. Oxidation of tert-butanol with potassium dichromate, in the presence of sulphuric acid, leads to butanoic acid. B. When alcohols are oxidized with potassium permanganate, in the presence of sulphuric acid, the colour of the reaction mixture turns form orange to green. C. 2-ketopentanoic acid and ...
Reductions of Carboxylic Acid Derivatives - IDC
... for the reduction of aldehydes and ketones to 1º and 2º-alcohols respectively has been noted. Of these, lithium aluminum hydride, often abbreviated LAH, is the most useful for reducing carboxylic acid derivatives. Thanks to its high reactivity, LAH easily reduces all classes of carboxylic acid deriv ...
... for the reduction of aldehydes and ketones to 1º and 2º-alcohols respectively has been noted. Of these, lithium aluminum hydride, often abbreviated LAH, is the most useful for reducing carboxylic acid derivatives. Thanks to its high reactivity, LAH easily reduces all classes of carboxylic acid deriv ...
679KB - NZQA
... one that is different, clearly describing how this property could be used to distinguish between the enantiomers. ...
... one that is different, clearly describing how this property could be used to distinguish between the enantiomers. ...
Chapter 20: Carboxylic Acids and Nitriles
... or Na2Cr2O7 gives a substituted benzoic acid (see Section 16.9) 1° and 2° alkyl groups can be oxidized, but tertiary groups are not ...
... or Na2Cr2O7 gives a substituted benzoic acid (see Section 16.9) 1° and 2° alkyl groups can be oxidized, but tertiary groups are not ...
IUPAC nomenclature of organic chemistry
... The IUPAC nomenclature of organic chemistry is a systematic method of naming organic chemical compounds as recommended[1] by the International Union of Pure and Applied Chemistry (IUPAC). Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be ...
... The IUPAC nomenclature of organic chemistry is a systematic method of naming organic chemical compounds as recommended[1] by the International Union of Pure and Applied Chemistry (IUPAC). Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be ...
Working with Hazardous Chemicals
... N,4,4-Trimethyl-2-oxazolinium iodide is prepared by adding 49.5 g. (0.500 mole) of 4,4-dimethyl-2oxazoline to an excess of cold methyl iodide (182 g., 78.2 ml., 1.28 moles) in a 500-ml. flask and stirring at room temperature under argon for 20 hours. The light brown solid is suction filtered and dis ...
... N,4,4-Trimethyl-2-oxazolinium iodide is prepared by adding 49.5 g. (0.500 mole) of 4,4-dimethyl-2oxazoline to an excess of cold methyl iodide (182 g., 78.2 ml., 1.28 moles) in a 500-ml. flask and stirring at room temperature under argon for 20 hours. The light brown solid is suction filtered and dis ...
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.