Organic Dyes as Photoredox Catalysts
... The Nicewicz group applied Mes–Acr+ as a photoredox catalyst for the intramolecular antiMarkovnikov hydroetherification and hydroamination of olefins to form cyclic ethers and amines, respectively.1 Intermolecular reactions with amines,2a carboxylic acids,1 and mineral acids2b are also possible unde ...
... The Nicewicz group applied Mes–Acr+ as a photoredox catalyst for the intramolecular antiMarkovnikov hydroetherification and hydroamination of olefins to form cyclic ethers and amines, respectively.1 Intermolecular reactions with amines,2a carboxylic acids,1 and mineral acids2b are also possible unde ...
Chapter 13 - U of L Class Index
... Select the longest carbon chain containing the hydroxyl group, and derive the parent name by replacing the –e of the corresponding alkane with –ol. ...
... Select the longest carbon chain containing the hydroxyl group, and derive the parent name by replacing the –e of the corresponding alkane with –ol. ...
CHEM 210 Nomenclature Lecture
... Some organic compounds are identified using common names that do not follow the IUPAC system of nomenclature. Many of these names were given long ago before the IUPAC system was adopted, and are still widely used. Additionally, some names are descriptive of shape and structure, like those below: ...
... Some organic compounds are identified using common names that do not follow the IUPAC system of nomenclature. Many of these names were given long ago before the IUPAC system was adopted, and are still widely used. Additionally, some names are descriptive of shape and structure, like those below: ...
Organic Chemistry Notes
... I.2.4 Why all the Organic Chemistry? We’re Engineers! There are several reasons we need to become more familiar with compounds. One reason is that engineers need to know what they are burning. Another reason is to better understand the impact of products of combustion. The photochemical smog mechan ...
... I.2.4 Why all the Organic Chemistry? We’re Engineers! There are several reasons we need to become more familiar with compounds. One reason is that engineers need to know what they are burning. Another reason is to better understand the impact of products of combustion. The photochemical smog mechan ...
Organic #2
... Draw and name the alcohol isomers of C4H10O Name the isomer that is resistant to oxidation. Classify this alcohol as primary, secondary or tertiary. Depending on reaction conditions, oxidation of butan-1-ol can give two different organic products. Name the functional group present in each of these p ...
... Draw and name the alcohol isomers of C4H10O Name the isomer that is resistant to oxidation. Classify this alcohol as primary, secondary or tertiary. Depending on reaction conditions, oxidation of butan-1-ol can give two different organic products. Name the functional group present in each of these p ...
Organic for Chem II
... trans-2-hexene (The double bond starts on carbon number 2. One counts from the end that gets to the C=C bond first.) ...
... trans-2-hexene (The double bond starts on carbon number 2. One counts from the end that gets to the C=C bond first.) ...
INTRODUCING ACYL CHLORIDES (acid
... Substitution of the chlorine atom by other groups Acyl chlorides are extremely reactive, and in their reactions the chlorine atom is replaced by other things. In each case, in the first instance, hydrogen chloride gas is produced as steamy acidic fumes. However, in some cases the hydrogen chloride g ...
... Substitution of the chlorine atom by other groups Acyl chlorides are extremely reactive, and in their reactions the chlorine atom is replaced by other things. In each case, in the first instance, hydrogen chloride gas is produced as steamy acidic fumes. However, in some cases the hydrogen chloride g ...
11 - MSU Chemistry
... Each of these compounds is an acetal, that is a molecule made from an aldehyde or ketone and two alcohol groups. Which compounds were used to make these acetals? ...
... Each of these compounds is an acetal, that is a molecule made from an aldehyde or ketone and two alcohol groups. Which compounds were used to make these acetals? ...
CHM230 OXIDATION OF CYCLOHEXANOL TO CYCLOHEXANONE
... graduated cylinder. The distillate should be a mixture of cyclohexanone and water that contains excess acetic acid. RECORD the boiling point of the cyclohexanone. Transfer the distillate to a separatory funnel or beaker. 6. Add 3.5 grams of sodium carbonate to neutralize any excess acetic acid, and ...
... graduated cylinder. The distillate should be a mixture of cyclohexanone and water that contains excess acetic acid. RECORD the boiling point of the cyclohexanone. Transfer the distillate to a separatory funnel or beaker. 6. Add 3.5 grams of sodium carbonate to neutralize any excess acetic acid, and ...
Chapter 20: Carboxylic Acids and Nitriles
... Most amines that have 3 different substituents on N are not resolved because the molecules interconvert by pyramidal inversion ...
... Most amines that have 3 different substituents on N are not resolved because the molecules interconvert by pyramidal inversion ...
Organic Chemistry Fifth Edition
... catalyzed dehydration of ethanol – also with other primary alcohols ...
... catalyzed dehydration of ethanol – also with other primary alcohols ...
Organic Chemistry II
... The order of relative reactivity of acyl compounds goes as follows: acyl chloride > acid anyhdride > ester > amide ...
... The order of relative reactivity of acyl compounds goes as follows: acyl chloride > acid anyhdride > ester > amide ...
Functional Group Naming Rules
... (Main sections of “Amines” and “Amides” only) The naming of hydrocarbons follows a few basic rules. However, when organic molecules contain functional groups, the situation is more complex. Often, the rules for naming molecules with functional groups are cumbersome. For example, what about an alkene ...
... (Main sections of “Amines” and “Amides” only) The naming of hydrocarbons follows a few basic rules. However, when organic molecules contain functional groups, the situation is more complex. Often, the rules for naming molecules with functional groups are cumbersome. For example, what about an alkene ...
Chapter 13 Introduction to Organic Chemistry and Hydrocarbon
... because the intermolecular forces holding the alkane molecules together are very weak London Dispersion forces (Van derWaals force). As a result of these weak intermolecular forces the temperature required to separate the molecules into the vapor state is low. The strength of Van der Waals forces is ...
... because the intermolecular forces holding the alkane molecules together are very weak London Dispersion forces (Van derWaals force). As a result of these weak intermolecular forces the temperature required to separate the molecules into the vapor state is low. The strength of Van der Waals forces is ...
Cis/Trans
... http://www.youtube.com/watch?v=1qGPWdm2M lI • The most common type of reaction for alkenes is addition: • general pattern – alkene + AB ---> see board ...
... http://www.youtube.com/watch?v=1qGPWdm2M lI • The most common type of reaction for alkenes is addition: • general pattern – alkene + AB ---> see board ...
8.1 Alcohols, Phenols, and Ethers
... ketones, the “–e” is dropped from the alkane containing the carbonyl group and replaced with the suffix “-one”. The location of the carbonyl group must be specified in ketones containing five or more carbons. The chain is numbered in a manner which places the lowest number on the carbon containing t ...
... ketones, the “–e” is dropped from the alkane containing the carbonyl group and replaced with the suffix “-one”. The location of the carbonyl group must be specified in ketones containing five or more carbons. The chain is numbered in a manner which places the lowest number on the carbon containing t ...
Ketones - Sanfordchemistrystudentwork
... ◦ These are alkenes with a hydroxyl group attached to one of the carbon atoms forming the double bond ◦ The enol is normally unstable, doesn’t survive long and changes into the keto ...
... ◦ These are alkenes with a hydroxyl group attached to one of the carbon atoms forming the double bond ◦ The enol is normally unstable, doesn’t survive long and changes into the keto ...
CHEMISTRY 314-01 MIDTERM # 4 April 15, 2003 Name
... (9 pts) Mark as true (T) or false (F) the following statements. Do not explain! • Fischer esterification occurs only in strongly basic conditions; • Amides are less reactive than acid chlorides but more reactive than esters; • Saponification is the process of base-catalyzed hydrolysis of esters; • L ...
... (9 pts) Mark as true (T) or false (F) the following statements. Do not explain! • Fischer esterification occurs only in strongly basic conditions; • Amides are less reactive than acid chlorides but more reactive than esters; • Saponification is the process of base-catalyzed hydrolysis of esters; • L ...
Solid phase reactions II
... Reduction of carboxylic acids (Weinreb amide) Oxidation of alcohols ...
... Reduction of carboxylic acids (Weinreb amide) Oxidation of alcohols ...
314_lect_26_tosyl_SN..
... groups or have more than eight electrons in its valence. However, there is a similar mechanism at carbon where trivalent carbon (sp2) of an acid chloride becomes tetravalent (sp3) in an intermediate and then goes back to being trivalent (sp2). That mechanism is presented in just a bit as a problem f ...
... groups or have more than eight electrons in its valence. However, there is a similar mechanism at carbon where trivalent carbon (sp2) of an acid chloride becomes tetravalent (sp3) in an intermediate and then goes back to being trivalent (sp2). That mechanism is presented in just a bit as a problem f ...
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.