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Topic 16 Test - A
Topic 16 Test - A

... How many structural isomers, which are aldehydes, have the molecular formula C5H10O? A ...
Remodeling of the natural product fumagillol
Remodeling of the natural product fumagillol

... Further optimization using La(OTf)3 and Zn(OTf)2 catalysts was next pursued. The transformations were robust and did not require inert atmosphere, nor special precautions for anhydrous solvent. Other nonpolar solvents provided similar regioselectivity, though toluene proved to be optimal, in which c ...
Reaction of orthoesters with alcohols in the presence of acidic
Reaction of orthoesters with alcohols in the presence of acidic

... also. As O-acetylation with orthoester is not hitherto a known reaction, we were curious to explore this to find out whether such a transformation could be useful as a synthetic methodology and the results are summarized in Table I. Thus the reaction of alcohols and orthoester with various acid cata ...
Abbreviated Chapter 17 Powerpoint
Abbreviated Chapter 17 Powerpoint

... • Alkyl groups are activating substituents and ortho, paradirectors. • This effect is called the inductive effect because alkyl groups can donate electron density to the ring through the sigma bond, making them more active. ...
Chapter 13 Silicon reagents
Chapter 13 Silicon reagents

... • Almost all acyclic Cl, Br, and I silanes react with all nucleophiles by an SN2 type mechanism leading to an inversion of configuration at the Si atom. • In many cases the pentacovalent Si is thought to be an intermediate rather than a transition state. ...
The aim of the work
The aim of the work

... with such CH-acid as - and -lactones in the presence of an alkaline catalyst. It is very well known and widely used reaction but only during the recent years there appeared a number of articles dedicated to the new type of aldehyde condensation reactions with CH-acid. It has been reported in the l ...
Nucleophilic substitution at saturated carbon
Nucleophilic substitution at saturated carbon

... Because a nucleophile substitutes for the halogen, these reactions are known as nucleophilic substitution reactions The reaction mechanism which predominates depends on the following factors: •  the structure of the alkyl halide •  the reactivity of the nucleophile •  the concentration of the nucle ...
Answers
Answers

...  Nucleophilic acyl substitutions can occur with weak nucleophiles under basic conditions, but only if the carboxylic acid derivative is very reactive  Nulceophilic acyl substitutions can occur with weak nucleophiles under acidic conditions  Carboxylic acids can be esterified with alcohols under a ...
Chapter 18 - Aldehydes and Ketones
Chapter 18 - Aldehydes and Ketones

... • Wittig Reaction (18.13) The Wittig reaction is the addition of a phosphorus ylide to the carbonyl. The initial reaction is quickly followed by the rearrangement of the intermediate into the alkene and a phosphine oxide. ...
T10 AD bioenergetics
T10 AD bioenergetics

... methanogenesis is from proton translocation via electron transfer to the methyl group generated during metabolism. Methanogenesis = anaerobic methyl respiration ...
Thiobenzoate Photochemistry
Thiobenzoate Photochemistry

... The failure of photoexcited 3 and 4 to undergo -H abstraction is likely due to constraints imposed by the fused ring systems. The added activation energy counteracts the weakly activating effects of the -alkoxy or -hydroxy groups. The photochemistry of the thiocarbonyl group has been documented i ...
Secondary alcohols
Secondary alcohols

... Esterification is the reaction of alcohols with carboxylic acids in the presence of catalytic amounts of a strong inorganic acid (H2SO4 or HCl) which yields esters and water. This is an equilibrium process which can be shifted in either ...
Title Carbonyl reduction with CaH2 and R3SiCl catalyzed by ZnCl2
Title Carbonyl reduction with CaH2 and R3SiCl catalyzed by ZnCl2

... In summary, we have demonstrated that CaH2/silyl chloride reduced carbonyl compounds in the presence of a catalytic amount of zinc salt.12 The cat. ZnX2/CaH2/R3SiCl system developed here is more general for carbonyl reduction than ...
Introduction to Chemical Reactions
Introduction to Chemical Reactions

... Examples of Decomposition Reactions ...
Organic Chemistry - Snow College | It's SNOWing
Organic Chemistry - Snow College | It's SNOWing

... • Uses a better leaving group • Conditions are not as extreme • Phosphorous oxychloride and pyridine • No rearrangements • Mildly basic conditions favor E2 ...
Chapter 7
Chapter 7

... sodium ethoxide in ethanol, it reacts rapidly; the product is 4-tert-butylcyclohexene. Under the same condition , trans1-bromo-4-ter-butylcyclohexane reacts very slowly. Write conformational structures and explain the difference in reactivity of these cis-trans isomers. ...
Ethers, Sulfides, Epoxides
Ethers, Sulfides, Epoxides

... as protecting groups for alcohols. Recall that the key step in forming the acetal was creating the carbocation as shown… There are other ways to create carbocations…… ...
Carbenes and Nitrenes: Structure, generaNon and reacNvity
Carbenes and Nitrenes: Structure, generaNon and reacNvity

... The  first  applica4ons  of  thiazolydenes  in  umpolung  organocatalysis  were  reported  as early  as  1943  (J.  Pharm.  Soc.  Jpn.  1943,  63,  296)  and  metal  complexes  of  NHCs  were already  reported  in  the  late  60’s.  Howeve ...
Answers - Final Exam 2013
Answers - Final Exam 2013

... b. An alkene will form the same epoxide upon treatment with either Br2 and H2O followed by base, or with MCPBA c. Rearrangements may occur during SN1 reactions, but not during SN2 reactions d. Rearrangements may occur during E2 reactions, but not during E1 reactions e. Carbocations may add to alkene ...
N-METAL COMPOUNDS
N-METAL COMPOUNDS

... metals with the cyclopentadienyl anion. Other metals that form sandwichtype structures similar to ferrocene include nickel, titanium, cobalt, ruthenium, zirconium, and osmium. The stability of metallocenes varies greatly with the metal and its oxidation state; ferrocene, ruthenocene, and osmocene ar ...
Rhenium(VII) Catalysis of Prins Cyclization Reactions
Rhenium(VII) Catalysis of Prins Cyclization Reactions

... Reaction was carried out with 1 mol % of O3ReOSiPh3. b Reaction was carried out with 30 mol % of VO(OPrn)3 instead of O3ReOSiPh3 and with 2 ...
HL  ISSN: 2231 – 3087(print) / 2230 – 9632 (Online)
HL ISSN: 2231 – 3087(print) / 2230 – 9632 (Online)

... We have carried out Mannich reaction of vanillin for the synthesis of 5-dimethylaminomethyl-4hydroxy-3-methoxybenzaldehyde by using dimethylamine and paraformaldehyde in methanol at room temperature. The Mannich base was then acetylated by refluxing it with acetic anhydride for about 24 hrs and the ...
ENGLISH VERSION Exam Organic Chemistry 2
ENGLISH VERSION Exam Organic Chemistry 2

... place on Wednesday June 4, 2007, at 10.00-12.00 in the Erdtman-room, Organic Chemistry, Teknikringen 30, Level 7. No special registration necessary. Please note that the minimum requirement for the course have to be demonstrated in this case also. The make-up exam will take place on Thursday August ...
CHEMISTRY 1000
CHEMISTRY 1000

... The alkoxide ion could alternately have been prepared by reacting the alcohol with sodium or potassium. This is usually done when the alcohol is also the solvent for the reaction. These reactions are analogous to the reactions between alkali metals and water that you studied in CHEM 1000. Do you rem ...
Synthesis of Ligands for the Functionalization of Magnetic
Synthesis of Ligands for the Functionalization of Magnetic

... The initial tests of the Mukaiyama-Aldol reaction provide valuable insight into the use of reusable catalysts. All three reactions are analyzed by 1H NMR. The NMR of the reaction with no ligand shows no product being made. This supports the necessity of the ligand in catalyzing the reaction. The NMR ...
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Vinylcyclopropane rearrangement



The vinylcyclopropane rearrangement or vinylcyclopropane-cyclopentene rearrangement is a ring expansion reaction, converting a vinyl-substituted cyclopropane ring into a cyclopentene ring.Intense experimental as well as computational investigations have revealed that mechanistically, the vinylcyclopropane rearrangement can be thought of as either a diradical-mediated two-step and/or orbital-symmetry-controlled pericyclic process. The amount by which each of the two mechanisms is operative is highly dependent on the substrate.Due to its ability to form cyclopentene rings the vinylcyclopropane rearrangement has served several times as a key reaction in complex natural product synthesis.
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