The first practical method for asymmetric epoxidation
... identical reaction conditions. However, for the less-reactive substrates in Table I (5a, 6a, and 7a), the “1-equiv” conditions described above were necessary to achieve reasonable reaction rates. Even under the “1-equiv” conditions, allylic alcohol 7a required almost 2 days to approach completion. F ...
... identical reaction conditions. However, for the less-reactive substrates in Table I (5a, 6a, and 7a), the “1-equiv” conditions described above were necessary to achieve reasonable reaction rates. Even under the “1-equiv” conditions, allylic alcohol 7a required almost 2 days to approach completion. F ...
organic chemistry i
... Addition of hydrogen halides. Markovnikov's rule. Regioselective reactions Addition of hydrogen bromide. Peroxide effect Addition of sulfuric acid Addition of water. Hydration Addition of alkanes. Alkylation Ozonolysis Analysis of alkenes ...
... Addition of hydrogen halides. Markovnikov's rule. Regioselective reactions Addition of hydrogen bromide. Peroxide effect Addition of sulfuric acid Addition of water. Hydration Addition of alkanes. Alkylation Ozonolysis Analysis of alkenes ...
Alcohols
... chain alcohols the effect of hydrogen bonding is minimized due to long nonpolar hydrocarbon portions. Therefore larger alcohols are good solvents for nonpolar molecules. Hydrogen bonding also gives alcohols a high boiling point when compared to their parent alkanes. Reactions of Alcohols 1. Prepar ...
... chain alcohols the effect of hydrogen bonding is minimized due to long nonpolar hydrocarbon portions. Therefore larger alcohols are good solvents for nonpolar molecules. Hydrogen bonding also gives alcohols a high boiling point when compared to their parent alkanes. Reactions of Alcohols 1. Prepar ...
Nucleophilic Substitution
... Nucleophilic substitution reactions are an important class of reactions that allow the interconversion of functional groups. Of particular importance are the reactions of alkyl halides (R-X) and alcohols (R-OH) For alcohols, the range of substitution reactions possible can be increased by utilising ...
... Nucleophilic substitution reactions are an important class of reactions that allow the interconversion of functional groups. Of particular importance are the reactions of alkyl halides (R-X) and alcohols (R-OH) For alcohols, the range of substitution reactions possible can be increased by utilising ...
Carbonyl Compounds
... - a solution of I2 in an alkaline medium such as NaOH or KOH is a oxidising agent. - when ethanal warmed with this solution, triiodoethanal will be formed as the intermediate product. - triiodoethanal then reacts with the base to form a yellow precipitate of triiodomethane (iodoform). CH3CHO + 3I2 ...
... - a solution of I2 in an alkaline medium such as NaOH or KOH is a oxidising agent. - when ethanal warmed with this solution, triiodoethanal will be formed as the intermediate product. - triiodoethanal then reacts with the base to form a yellow precipitate of triiodomethane (iodoform). CH3CHO + 3I2 ...
Study on the Reduction of Molybdenum Dioxide by Hydrogen
... to the left side. Thus, Fig. 1 points out the fact that the driving force of the reaction (1) for an arbitrary atmosphere of flue gas in the reaction system increases with increase in the reaction temperature. Figure 2 presents the reduction ratio of MoO2 calculated from the mass change of oxygen occ ...
... to the left side. Thus, Fig. 1 points out the fact that the driving force of the reaction (1) for an arbitrary atmosphere of flue gas in the reaction system increases with increase in the reaction temperature. Figure 2 presents the reduction ratio of MoO2 calculated from the mass change of oxygen occ ...
reactions of functional groups of organic compounds with
... Oxidation of primary alcohols and aldehydes Primary alcohols are oxidized to Carbonyl group compounds - aldehydes. In practice it was used for detection of ethanol in breath – acidified orange potassium dichromate (Cr(VI)) is reduced to green colored solution (Cr(III)) in presence of alcohol (which ...
... Oxidation of primary alcohols and aldehydes Primary alcohols are oxidized to Carbonyl group compounds - aldehydes. In practice it was used for detection of ethanol in breath – acidified orange potassium dichromate (Cr(VI)) is reduced to green colored solution (Cr(III)) in presence of alcohol (which ...
Organic Chemistry II
... 3.3.2 Halogenation at the α Carbon . . . . . . . . . . . . . . . . . 3.3.3 The Haloform Reaction . . . . . . . . . . . . . . . . . . . . . 3.4 Lithium Enolates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5 Enolates of β -Dicarbonyl Compounds . . . . . . . . . . . . . . . . . 3.6 Synt ...
... 3.3.2 Halogenation at the α Carbon . . . . . . . . . . . . . . . . . 3.3.3 The Haloform Reaction . . . . . . . . . . . . . . . . . . . . . 3.4 Lithium Enolates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.5 Enolates of β -Dicarbonyl Compounds . . . . . . . . . . . . . . . . . 3.6 Synt ...
Aldehydes and ketones
... In these compounds, the carbonyl group is bound to a nitrogen (an amino group), in addition to either a H-atom or a carbon group (alkyl, cycloalkyl, aromatic). The R’ and R” groups of the amino group may either be H or carbon groups: General formula for an amide: ...
... In these compounds, the carbonyl group is bound to a nitrogen (an amino group), in addition to either a H-atom or a carbon group (alkyl, cycloalkyl, aromatic). The R’ and R” groups of the amino group may either be H or carbon groups: General formula for an amide: ...
Chemistry 250A -- Exam #3 Answer Key -
... hydrogen in this orientation and therefore elimination proceeds to give only the product shown. By contrast, the second reaction proceeds via an E1 mechanism as shown below. (The absence of a strong base makes the E2 mechanism unfavorable.) In the E1 mechanism the leaving group leaves first, produci ...
... hydrogen in this orientation and therefore elimination proceeds to give only the product shown. By contrast, the second reaction proceeds via an E1 mechanism as shown below. (The absence of a strong base makes the E2 mechanism unfavorable.) In the E1 mechanism the leaving group leaves first, produci ...
Exam 2
... 1. (10 pts) Circle what is true about Substitution and elimination reactions. a. Strong Bases (B") have conjugate acids (BH) that have small pKa values (<5) ...
... 1. (10 pts) Circle what is true about Substitution and elimination reactions. a. Strong Bases (B") have conjugate acids (BH) that have small pKa values (<5) ...
Fundamentals Of Organic Chemistry
... Mechanism of the dehydration of alcohol is discussed below, and also in elimination reactions, later in this book. Mechanism Protonation of the hydroxyl group of the alcohol followed by the loss of water molecule to give a 1° carbocation. The 1° carbocation undergo rearrangement to form more stable ...
... Mechanism of the dehydration of alcohol is discussed below, and also in elimination reactions, later in this book. Mechanism Protonation of the hydroxyl group of the alcohol followed by the loss of water molecule to give a 1° carbocation. The 1° carbocation undergo rearrangement to form more stable ...
Article Summaries
... details of the C-H activation step (whether it proceeds via an electrophilic or oxidative addition pathway) were not resolved. ______________________________________________________________________________ Shilov, A.E.; Shteinman A.A. Acc. Chem. Res. 1999, 32, 763-771. This paper discusses the vario ...
... details of the C-H activation step (whether it proceeds via an electrophilic or oxidative addition pathway) were not resolved. ______________________________________________________________________________ Shilov, A.E.; Shteinman A.A. Acc. Chem. Res. 1999, 32, 763-771. This paper discusses the vario ...
ELECTROPHILIC ADDITIONS OF ALKENES AS THE
... of these reactons are electrophilic additions, or the addition of electrophiles across the double bond. Several of these reactions amount to addition of water to the p-bond. The result is the transformation of alkenes into alcohols. We now look at the generalities of this type of reaction (electroph ...
... of these reactons are electrophilic additions, or the addition of electrophiles across the double bond. Several of these reactions amount to addition of water to the p-bond. The result is the transformation of alkenes into alcohols. We now look at the generalities of this type of reaction (electroph ...
Bk3BP08EE
... The nucleophilic ammonia attacks the partially positive carbon to which the electronegative chlorine is attached resulting in the formation of a pentavalent transition state. The C – Cl bond is being broken as the C – N bond is formed. The resultant organic product is ethylamine, CH3CH2NH2. The amin ...
... The nucleophilic ammonia attacks the partially positive carbon to which the electronegative chlorine is attached resulting in the formation of a pentavalent transition state. The C – Cl bond is being broken as the C – N bond is formed. The resultant organic product is ethylamine, CH3CH2NH2. The amin ...
Holt Modern Chemistry -
... o Radioactive nuclides, such as cobalt-60, are used to destroy certain types of cancer cells. Other radioactive nuclides serve as radioactive tracers. A tracer is incorporated into another material and moves with its particles. Radioactive tracers can reveal how well substances are passing through t ...
... o Radioactive nuclides, such as cobalt-60, are used to destroy certain types of cancer cells. Other radioactive nuclides serve as radioactive tracers. A tracer is incorporated into another material and moves with its particles. Radioactive tracers can reveal how well substances are passing through t ...
Dehydration of Cyclohexanol
... dehydration, an E1 reaction. In this experiment, a mixture of concentrated phosphoric acid and concentrated sulfuric acid is used to prepare cyclohexene from cyclohexanol via an E1 reaction. The mechanism of this E1 reaction involves three steps. First, is the rapid (and reversible) protonation of t ...
... dehydration, an E1 reaction. In this experiment, a mixture of concentrated phosphoric acid and concentrated sulfuric acid is used to prepare cyclohexene from cyclohexanol via an E1 reaction. The mechanism of this E1 reaction involves three steps. First, is the rapid (and reversible) protonation of t ...
Enthalpy Review Questions
... to a vapor at that temperature? (The specific heat of liquid ethanol is 2.44 J/g K, and the enthalpy of vaporization is 38.56 kJ/mol.) 3. Methanol, CH 3OH, is a possible automobile fuel. The alcohol produces energy in a combustion reaction with O2: 2CH3OH(g) + 502 (g) sssssd 2 CO2(g) + 4 H2O(g) A 0. ...
... to a vapor at that temperature? (The specific heat of liquid ethanol is 2.44 J/g K, and the enthalpy of vaporization is 38.56 kJ/mol.) 3. Methanol, CH 3OH, is a possible automobile fuel. The alcohol produces energy in a combustion reaction with O2: 2CH3OH(g) + 502 (g) sssssd 2 CO2(g) + 4 H2O(g) A 0. ...
WRL0437.tmp
... Alkyl halides are most commonly synthesized from alcohols by replacing the hydroxyl group with a halide substituent. This is an example of nucleophilic aliphatic substitution, which is part of a very important group of reactions. The overall reaction is the same, but the mechanism varies depending o ...
... Alkyl halides are most commonly synthesized from alcohols by replacing the hydroxyl group with a halide substituent. This is an example of nucleophilic aliphatic substitution, which is part of a very important group of reactions. The overall reaction is the same, but the mechanism varies depending o ...
Microsoft Word
... 30. This is generally prepared by O-methylation of β-naphthol 29 which is carried out by using highly toxic methylating agents such as methyl halides or dimethyl sulfate and a base such as sodium hydroxide. In the present work, we have used dimethyl carbonate as the methylating agent. Dimethyl carbo ...
... 30. This is generally prepared by O-methylation of β-naphthol 29 which is carried out by using highly toxic methylating agents such as methyl halides or dimethyl sulfate and a base such as sodium hydroxide. In the present work, we have used dimethyl carbonate as the methylating agent. Dimethyl carbo ...
PDF document
... presented in Figure 2. Before the oxidation, there is an oilwater biphasic system, and the bottom layer (aqueous phase) consists of PEG1000-DAIL and hydrogen peroxide. PEG1000-DAIL catalytic system is completely dissolved in aqueous phase, and the upper layer (oil phase) consists of toluene and prim ...
... presented in Figure 2. Before the oxidation, there is an oilwater biphasic system, and the bottom layer (aqueous phase) consists of PEG1000-DAIL and hydrogen peroxide. PEG1000-DAIL catalytic system is completely dissolved in aqueous phase, and the upper layer (oil phase) consists of toluene and prim ...
Option G Further Organic Chemistry
... The compounds and reaction types in this option at SL are summarized in the following ...
... The compounds and reaction types in this option at SL are summarized in the following ...
Chapter 11
... Therefore often need to add an additional Lewis acid to convert an alcohol to alkyl chloride (even with 2˚ and 3˚ alcohols that proceed through SN1) ...
... Therefore often need to add an additional Lewis acid to convert an alcohol to alkyl chloride (even with 2˚ and 3˚ alcohols that proceed through SN1) ...
Alcohols I Reading: Wade chapter 10, sections 10-1- 10
... Lithium Aluminum Hydride (LiAlH4) is a stronger reducing agent than sodium borohydride that can reduce all carbonyl compounds. Ketones are reduced to 2° alcohols; all other carbonyl compounds (aldehydes, esters, acids, acid chlorides) are reduced to primary alcohols. O ...
... Lithium Aluminum Hydride (LiAlH4) is a stronger reducing agent than sodium borohydride that can reduce all carbonyl compounds. Ketones are reduced to 2° alcohols; all other carbonyl compounds (aldehydes, esters, acids, acid chlorides) are reduced to primary alcohols. O ...
Wolff–Kishner reduction
The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step. As such, there is no obvious retron for this reaction. Originally reported by Nikolai Kischner in 1911 and Ludwig Wolff in 1912, it has been applied to the total synthesis of scopadulcic acid B, aspidospermidine and dysidiolide.In general, the reaction mechanism first involves the in situ generation of a hydrazone by condensation of hydrazine with the ketone or aldehyde substrate. Sometimes it is however advantageous to use a pre-formed hydrazone as substrate (see modifications). The hydrazone is deprotonated by alkoxide base followed by a concerted, rate-determining step in which a diimide anion is formed. Collapse of this alkyldiimde with loss of N2 leads to formation of an alkylanion which can be protonated by solvent to give the desired product.Because the Wolff–Kishner reduction requires highly basic conditions, it is unsuitable for base-sensitive substrates. However, this method can be superior over the related Clemmensen reduction for acid-sensitive compounds such as pyrroles and for high-molecular weight compounds.