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07. Aldehydes and ketones
07. Aldehydes and ketones

... Physical properties of aldehydes and ketones Methods of aldehydes and ketones obtaining. Chemical properties of aldehydes and ketones Unsaturated aldehydes and ketones. Chemical properties of unsaturated aldehydes and ketones. Dialdehydes and diketones. Nomenclature of aromatic aldehydes and ketones ...
Functional Groups
Functional Groups

... If necessary, identify the carbon to which the carboxyl group is attached. ...
Grant MacEwan College - Faculty Web Pages
Grant MacEwan College - Faculty Web Pages

... Description: This is the second course in organic chemistry. The topics covered include structural and chemical properties of alkenes, alkynes, alcohols, phenols, ethers, aromatic compounds. Aldehyde, ketones, amines, carboxylic acids, and carboxylic acid derivatives. Illustration of these functiona ...
A Model for Catalytically Active Zinc(I1) Ion in Liver
A Model for Catalytically Active Zinc(I1) Ion in Liver

... CloH24N4Zn(CF3S03)2: C, 25.56; H, 4.29; N, 9.94. Found: C, 25.53; H, 4.34; N , 9.97. Reactions of p -Nitrobenzaldehyde (9) with Alcohols Catalyzed by Various Zn" Species. p-Nitrobenzaldehyde (9,0.125 mmol) was added in one portion to a 1.0 mL alcohol solution of a Zn" catalyst (total [Zn"] = 1 mM). ...
Chapter 16: Ethers, Epoxides, and Sulfides
Chapter 16: Ethers, Epoxides, and Sulfides

... The sulfur atom of sulfides is much more nucleophilic than the oxygen atom of ethers, and will react with alkyl halides to give stable sulfonium salts. H3C ...
Synopsis
Synopsis

... corresponding sulfoxides has been developed though non stereoselectively. The diastereomeric sulfilimines behave in a stereoconvergent fashion and afford products with the same configuration at carbon. An efficient route to αhydroxy-β-amino acid derivatives AHDA and AHPBA was developed using a commo ...
using hydrogen as a nucleophile in hydride reductions
using hydrogen as a nucleophile in hydride reductions

Substitution Rxns-a-Sn2-12-quesx
Substitution Rxns-a-Sn2-12-quesx

Aldehydes & Ketones
Aldehydes & Ketones

... • The aldehydes and ketones are characterized by the presence of the carbonyl group. • The carbonyl group is a functional group made up of a carbon atom bonded to an oxygen atom by a double bond. • Carbonyl compounds are those that contain a carbonyl group. • Aldehydes, ketones, carboxylic acids, an ...
Exam 2
Exam 2

Carbonyls
Carbonyls

Organic Chemistry II
Organic Chemistry II

... When the reagent is a strong nucleophile, addition takes place as follows without stereospecicity: ...
Example
Example

...  Very strong C═O stretch around 1710 cm-1 for ketones and 1725 cm-1 for simple aldehydes  Additional C—H stretches for aldehyde: Two absorptions at 2710 cm-1 and 2810 cm-1 © 2013 Pearson Education, Inc. ...
THIOALCOHOLS AND DISULFIDES:
THIOALCOHOLS AND DISULFIDES:

... Alcohols add to the carbonyl group of aldehydes and ketones to form hemiacetals and hemiketals respectively. Hemiacetals contain both an alcohol and ether functional group in the same carbon. The two groups are so close to each other that they modify each other’s properties. So we have neither an or ...
New L-Serine Derivative Ligands as Cocatalysts for Diels
New L-Serine Derivative Ligands as Cocatalysts for Diels

Chapter 7: Alkene reactions
Chapter 7: Alkene reactions

... Chapter 7: Alkene reactions – conversion to new functional groups Preparation of alkenes: two common elimination reactions 1. Dehydration of alcohols Dehydration is a common biochemical reaction in carbohydrate and fatty acid metabolism and terpene biosynthesis – it’s catalyzed in vivo by specific e ...
Nucleophilic Additions to Carbonyl Group
Nucleophilic Additions to Carbonyl Group

... group itself. Thus, even a nucleophile that is not very reactive with a carbonyl reacts readily with the conjugate acid. Of the seven functional groups containing a carbonyl group, only aldehydes and ketones commonly undergo nucleophilic addition. The remaining five carbonyl functional groups underg ...
Introduction to Organic Synthesis 2011
Introduction to Organic Synthesis 2011

... The formation of new C-C bond(s) Having looked at radical reactions in previous lectures we now going to go back to reactions involving the transfer of electron pairs. Hence these are reactions that involve the use of nucleophiles. Nucleophiles donates electrons, but can often react as bases as wel ...
Experiment #9 – Identification of Aldehydes and Ketones
Experiment #9 – Identification of Aldehydes and Ketones

... Aldehydes and ketones share the carbonyl functional group which features carbon doubly bonded to oxygen. In the case of ketones there are two carbon atoms bonded to the carbonyl carbon and no hydrogens. In the case of aldehydes there is at least one hydrogen bonded to the carbonyl carbon; the other ...
CHEM 263 (AS 40) Organic Chemistry II Winter 2017 Instructor: Dr
CHEM 263 (AS 40) Organic Chemistry II Winter 2017 Instructor: Dr

... Course Description: (3 credits). The nomenclature, structure, physical properties, synthesis and selected reactions of the basic functional groups in organic chemistry are discussed. Functional groups covered include alkenes, alkynes, aromatic compounds, alcohols, phenols, ethers, aldehydes, ketones ...
Document
Document

ch12 by dina
ch12 by dina

... Planning a Grignard Synthesis  Example : Synthesis of 3-phenyl-3-pentanol  The starting material may be a ketone or an ester  There are two routes that start with ketones (one is shown) ...
Document
Document

... 2.29 Predict the IR absorption bands which would allow to distinguish the pair of compounds in a), c), d), e), g), i): a) ...
Synthesis of (−)-Epibatidine - David A. Evans
Synthesis of (−)-Epibatidine - David A. Evans

... syntheses have been reported, few full syntheses are enantioselective.4 In this Letter, we wish to report a highly stereoselective synthesis of (-)-epibatidine by a route that is readily amenable to analogue production. Our approach to 1 relies on a selective hetero Diels-Alder reaction between bis- ...
Exam III
Exam III

... stereospecific reactions, be able to show the structures for the alkene reactants. -given the structures of the reactants and the products be able to state whether a reaction is syn- or anti-. ...
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1,3-Dipolar cycloaddition

The 1,3-dipolar cycloaddition is a chemical reaction between a 1,3-dipole and a dipolarophile to form a five-membered ring. The earliest 1,3-dipolar cycloadditions were described in the late 19th century to the early 20th century, following the discovery of 1,3-dipoles. Mechanistic investigation and synthetic application were established in the 1960s, primarily through the work of Rolf Huisgen. Hence, the reaction is sometimes referred to as the Huisgen cycloaddition (this term is often used to specifically describe the 1,3-dipolar cycloaddition between an organic azide and an alkyne to generate 1,2,3-triazole). Currently, 1,3-dipolar cycloaddition is an important route to the regio- and stereoselective synthesis of five-membered heterocycles and their ring-opened acyclic derivatives.
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