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Microsoft Word
Microsoft Word

... bases, inorganic bases, quaternary ammonium salts, protic and aprotic solvents and solventless conditions have been used to name a few. The main limitations in this process are the use of stoichiometric amount of base to substrate and non-regeneration of the catalyst. In this regard, a truly heterog ...
The Aldol Condensation Preparation of 4
The Aldol Condensation Preparation of 4

INTRODUCING ALCOHOLS
INTRODUCING ALCOHOLS

... the dichromate(VI) ions is reduced to a green solution containing chromium(III) ions. The electron-half-equation for this reaction is ...
or H - No Brain Too Small
or H - No Brain Too Small

... o the removal of water (H and OH on adjacent C atoms) to form a C=C bond o heat with conc. H2SO4 or pass over Al2O3 catalyst o since it involves removal it is also an elimination reaction elimination – @ level 2 this is limited to removal of water: o H & OH / water / removed from neighbouring C atom ...
Electophilic Aromatic Substituion
Electophilic Aromatic Substituion

... Substitution of H by SO3 (sulfonation) Reaction with a mixture of sulfuric acid and SO3 Reactive species is sulfur trioxide or its conjugate acid Reaction occurs via Wheland intermediate and is ...
C3 3.1-3.4 part 1 Alcohols, carboxlic acids and esters progress ticket
C3 3.1-3.4 part 1 Alcohols, carboxlic acids and esters progress ticket

enzymes lecture 4
enzymes lecture 4

...  Lactase acts on lactose.  Sucrase acts on sucrose.  Maltase acts on maltose. ...
7. Alkenes: Reactions and Synthesis
7. Alkenes: Reactions and Synthesis

... as the electrophile) to give a 1,2-halo alcohol, called a halohydrin  The actual reagent is the dihalogen (Br2 or Cl2 in water or in an organic solvent) ...
Name Dehydration Synthesis
Name Dehydration Synthesis

... 1. The  JOINING  of  two  monomers  causes  a  water  molecule  to  be  lost.    This  joining  to  make  a  polymer  is   called  DEHYDRATION  SYNTHESIS_.   2. The  SPLITTING  apart  of  two  organic  molecules  in  a  polymer  and ...
Chapter 20 Carboxylic Acids - chemistry
Chapter 20 Carboxylic Acids - chemistry

... • Oxidation of primary alcohols and aldehydes with chromic acid. • Cleavage of an alkene with hot KMnO4 produces a carboxylic acid if there is a hydrogen on the double-bonded carbon. • Alkyl benzene oxidized to benzoic acid by hot KMnO4 or hot chromic acid. ...
Chapter 1--Title
Chapter 1--Title

... Most anhydrides are named by dropping the word acid from the carboxylic acid name and adding the word anhydride ...
Chapter 19: Carboxylic Acids
Chapter 19: Carboxylic Acids

Organocatalysed asymmetric Mannich reactions
Organocatalysed asymmetric Mannich reactions

Organic Chemistry Unit Test – Tuesday October 7
Organic Chemistry Unit Test – Tuesday October 7

... p. 95 Chapter 1 Self Quiz Chapter 1 Review Questions pp. 96 – 97 # 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 16(a) Unit Review pp. 150 – 151 Unit 1 Self Quiz # 1, 2, 3, 4, 5, 6, 7, 11, 12, 13, 14, 16, 17, 19, 20, 21, 22 Unit Review Questions pp. 152 – 155 # 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 21, 22, 28 ...
o-chem - WordPress.com
o-chem - WordPress.com

... presence of oxides of V,Mo or Cr gives benzene and its homologues. • This reaction is known as aromatization . ...
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Question paper - Edexcel

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Chapter16McMurryPPP
Chapter16McMurryPPP

... The addition of bromine occurs in two steps In the first step the  electrons act as a nucleophile toward Br2 (in a complex with FeBr3) This forms a cationic addition intermediate from benzene and a bromine cation The intermediate is not aromatic and therefore high in energy (see Figure 16.2) ...
COOH HOOC COOH HOOC
COOH HOOC COOH HOOC

... 2. Decarboxylation = elimination of carbon dioxide from acids or their salts at high temperatures in the presence of NaOH R−COONa + NaOH  R−H + Na2CO3 ...
Additional Information on the Synthesis of Esters
Additional Information on the Synthesis of Esters

... assessed by refractive index. Also further practice in obtaining and interpreting infrared spectra and 1H-NMR will be provided. ...
Aldehid dan Keton
Aldehid dan Keton

... Aldehydes and ketones react reversibly with water to give 1,1-diols, or geminal (gem) diols • Equilibrium favors carbonyl compound for steric reasons with the exception of formaldehyde ...
Exam Name___________________________________
Exam Name___________________________________

... ESSAY. Write your answer in the space provided or on a separate sheet of paper. 55) Using ethanol as your only source of carbon compounds and using any other necessary inorganic reagents, propose a synthesis of ethyl acetate. 56) Using ethanol as your only source of carbon compounds and using any ot ...
Chapter 19
Chapter 19

... Amine salts are also used to catalyze a variety of organic reactions that feature two components that are soluble in different liquid phases (e.g. organic and aqueous) ...
Review Chapter 19
Review Chapter 19

(Organic Chemistry II) Pahlavan
(Organic Chemistry II) Pahlavan

... shown in equation (3). Acid anhydride, which is made by the removal of a water molecule from two acetic acid molecules, reacts with alcohols in much the same way as acids to form the ester. Drug manufacturers prepare aspirin from salicylic acid by this method, which is a much better synthetic method ...
6.5. alcohols
6.5. alcohols

... When ketones have 5C’s or more in a chain then it needs a number to show the position of the double bond. E.g. pentan-2-one ...
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Petasis reaction



The Petasis reaction (alternatively called the Petasis borono–Mannich (PBM) reaction) is the chemical reaction of an amine, aldehyde, and vinyl- or aryl-boronic acid to form substituted amines.Reported in 1993 by Nicos Petasis as a practical method towards the synthesis of a geometrically pure antifungal agent, naftifine, the Petasis reaction can be described as a variation of the Mannich reaction. Rather than generating an enolate to form the substituted amine product, in the Petasis reaction, the vinyl group of the organoboronic acid serves as the nucleophile. In comparison to other methods of generating allyl amines, the Petasis reaction tolerates a multifunctional scaffold, with a variety of amines and organoboronic acids as potential starting materials. Additionally, the reaction does not require anhydrous or inert conditions. As a mild, selective synthesis, the Petasis reaction is useful in generating α-amino acids, and is utilized in combinatorial chemistry and drug discovery.
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