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Aldehydes alcohol

Iron(III) chloride forms numerous addition compounds, especially with organic molecules which contain donor atoms, for example ethers, alcohols, aldehydes, ketones and amines. Anhydrous iron(III) chloride is soluble in, for example, ether, and can be extracted into this solvent from water the extraction is more effective in presence of chloride ion. Of other iron(III) halides, iron(III) bromide and iron(III) iodide decompose rather readily into the +2 halide and halogen. [Pg.394]

Monohydric alcohols, aldehydes (including chloral hydrate), ketones, cinnamic acid, amines (2-naphthylaminc is odourless), nitrophenols (resemble both phenol and nitro-compound),... [Pg.403]

The type of alcohol produced depends on the carbonyl compound Substituents present on the carbonyl group of an aldehyde or ketone stay there—they become sub stituents on the carbon that bears the hydroxyl group m the product Thus as shown m Table 14 3 (following page) formaldehyde reacts with Grignard reagents to yield pri mary alcohols aldehydes yield secondary alcohols and ketones yield tertiary alcohols... [Pg.595]

Hydrogen bonding m carboxylic acids raises their melting points and boiling points above those of comparably constituted alkanes alcohols aldehydes and ketones... [Pg.821]

This chapter is divided into two parts The first and major portion is devoted to carbohydrate structure You will see how the principles of stereochemistry and confer matronal analysis combine to aid our understanding of this complex subject The remain der of the chapter describes chemical reactions of carbohydrates Most of these reactions are simply extensions of what you have already learned concerning alcohols aldehydes ketones and acetals... [Pg.1026]

Chemical Properties. A combination of excellent chemical and mechanical properties at elevated temperatures result in high performance service in the chemical processing industry. Teflon PEA resins have been exposed to a variety of organic and inorganic compounds commonly encountered in chemical service (26). They are not attacked by inorganic acids, bases, halogens, metal salt solutions, organic acids, and anhydrides. Aromatic and ahphatic hydrocarbons, alcohols, aldehydes, ketones, ethers, amines, esters, chlorinated compounds, and other polymer solvents have Httle effect. However, like other perfluorinated polymers,they react with alkah metals and elemental fluorine. [Pg.375]

In the early 1920s Badische Arulin- und Soda-Fabrik aimounced the specific catalytic conversion of carbon monoxide and hydrogen at 20—30 MPa (200—300 atm) and 300—400°C to methanol (12,13), a process subsequendy widely industrialized. At the same time Fischer and Tropsch aimounced the Synth in e process (14,15), in which an iron catalyst effects the reaction of carbon monoxide and hydrogen to produce a mixture of alcohols, aldehydes (qv), ketones (qv), and fatty acids at atmospheric pressure. [Pg.79]

In the presence of base, di-Z f/-alkyl peroxides are stable, however primary and secondary diaLkyl peroxides undergo oxygen—oxygen bond cleavage, forming alcohols, aldehydes, and ketones (44,66) ... [Pg.108]

Biomters are most economic when apphed to low-concentration gas streams (<1000 ppm) that are also oxygen rich. Greater than 90 percent destruction efficiencies can be obtained for water-soluble organics such as alcohols, aldehydes, and amines. Water-soluble inor-... [Pg.2191]

Electrolysis, Bu4N Br, H2O, CH3CN, NaHC03- This method is unsatisfactory for primary and secondary alcohols, aldehydes, olefins, or amines. [Pg.188]

Most organic compounds are water-insoluble. Notable exceptions are the lower molecular weight alcohols, aldehydes, and ketones, all known to be "polar" molecules. This characteristic is of importance to firefighting because the specific gravity of the compound will then be a major determinant of the suitability of water for the suppression of fires involving the chemical. [Pg.168]

Liquids.—It may be a hydrocarbon (paraffin,olefine,aromatic) Jiiyher alcohol e.g. amyl alcohol), aldehyde [eg., benzaldehyde) ketone [eg., acetophenone) acid [e.g., valeric acid), ether, cdei, phenol [e.g., zveewtiCxaX) phenol ether [e.g, anisole). [Pg.332]

Solids. —It may Idc a hydrocM bon (c .g., paraffin wa, naphthalene) highei alcohol eg., cetyl alcohol) aldehyde e.g., z5-hydroxybenzaldehyde) ketone and qiiinonc e.g., benzo-phenone, camphor) acid (higher fatty, e.g., palmitic acid or aromatic acid) ester (of glycerol, phenols or aromatic alcohols) phenol e.g., thymol),... [Pg.336]

A number of the aldehydes, both of the aliphatic and aromatic series, are of the highest importance in synthetic perfumery. The relationship existing between alcohols, aldehydes, and acids is shown by the following example —... [Pg.177]

Like propane, the noncatalytic oxidation of butane yields a variety of products including organic acids, alcohols, aldehydes, ketones, and olefins. Although the noncatalytic oxidation of butane produces mainly aldehydes and alcohols, the catalyzed oxidation yields predominantly acids. [Pg.175]


See other pages where Aldehydes alcohol is mentioned: [Pg.445]    [Pg.1026]    [Pg.1091]    [Pg.184]    [Pg.816]    [Pg.182]    [Pg.469]    [Pg.475]    [Pg.22]    [Pg.317]    [Pg.335]    [Pg.338]    [Pg.305]    [Pg.241]    [Pg.379]    [Pg.493]    [Pg.493]    [Pg.495]    [Pg.108]    [Pg.506]    [Pg.300]    [Pg.408]    [Pg.21]    [Pg.257]    [Pg.530]    [Pg.2094]    [Pg.61]    [Pg.184]    [Pg.133]    [Pg.541]    [Pg.295]    [Pg.594]   
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See also in sourсe #XX -- [ Pg.92 ]

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ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION

ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH

ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE

ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE: 1-HEPTANAL

Acetals are formed from aldehydes or ketones plus alcohols in the presence of acid

Alcohol To aldehyde

Alcohol aldehyde pair

Alcohol and aldehyde

Alcohol and aldehyde decarbonylation

Alcohol and aldehyde dehydrogenases

Alcohol and aldehyde oxidation

Alcohol dehydrogenase aldehyde dehydrogenases

Alcohol dehydrogenase aldehyde reduction

Alcohol, Aldehyde-Free

Alcohol, alkenes => aldehydes

Alcohol-aldehyde dehydrogenases

Alcohols aldehydes (from prim

Alcohols aldehydes (prim

Alcohols aldehydes and ketones

Alcohols aldehydes, bisulfite

Alcohols by reduction of aldehydes

Alcohols enantioselective synthesis, from aldehyd

Alcohols from aldehyde hydrogenation

Alcohols from aldehyde hydrosilylation

Alcohols from aldehydes

Alcohols from aldehydes and ketones

Alcohols olefinic aldehydes

Alcohols oxidation to aldehydes

Alcohols preparation from aldehydes

Alcohols to aldehydes and

Alcohols to aldehydes and ketones

Alcohols via aldehydes

Alcohols with aldehydes and ketones

Alcohols, Aldehydes, Ketones, Ethers, and Amines

Alcohols, Aldehydes, Ketones, Quinones

Alcohols, From reduction of aldehydes Reagents which can be used to reduce

Alcohols, Thiols, Ethers, Aldehydes, and Ketones

Alcohols, allylic => aldehydes

Alcohols, amino from nitro aldehydes

Alcohols, aryl => aldehydes

Alcohols, homoallylic, chiral aldehydes

Alcohols, oxidizing reagents aldehydes

Alcohols, preparation by reduction of aldehydes

Aldehyde From allylic alcohol

Aldehyde From allylic alcohol (one carbon

Aldehyde alcohols with

Aldehyde and secondary alcohols

Aldehydes (s. a. Aldehyde alcohols, prim

Aldehydes (s. a. Formyl alcohols, sec. 8, 713 suppl

Aldehydes 1,2-amino alcohols

Aldehydes alcohol oxidation

Aldehydes alcohol oxidations, 2-iodoxybenzoic acid

Aldehydes alcohol synthesis from

Aldehydes alcohol synthesis, lithium aluminum hydride

Aldehydes alcohols by oxidation

Aldehydes alcohols, reduction

Aldehydes alkylation with alcohols

Aldehydes can react with alcohols to

Aldehydes can react with alcohols to form hemiacetals

Aldehydes chiral amino alcohol catalyzed

Aldehydes chromium trioxide + alcohols

Aldehydes from allylic alcohols, arylation

Aldehydes from primary alcohols

Aldehydes from tetrahydropyranyl alcohols

Aldehydes oxidation of primary alcohols

Aldehydes primary alcohol oxidations

Aldehydes reaction with alcohols

Aldehydes reduction to alcohols

Aldehydes synthesis of homoallylic alcohols

Aldehydes to unsaturated alcohols

Aldehydes via selective oxidation of primary alcohols

Aldehydes, Ketones, Alcohols, and. Carboxylic Acids

Aldehydes, preparation from primary alcohols

Aldehydes, reductive alkylation with alcohols

Alkene aldehydes from diene alcohols

Alkenyl Alcohols to Aldehydes and Ketones

Alkyne-alcohols => aldehydes

Alkyne-alcohols, dehydration aldehydes

Aluminum alkoxides, aldehydes from, with alcohols

Amino alcohol ligands aldehyde synthesis

Amino alcohol with aldehyde

Amino alcohols nitro aldehydes

Analysis of Alcohols and Aldehydes

Aromatic Aldehydes, Ketones and Alcohols

Benzylic alcohols from aromatic aldehydes

Biological reaction, alcohol aldehyde reduction

Chiral alcohols from aldehydes

Chromic acid, aldehydes from, with alcohols

Coniferyl aldehyde/alcohol

Copper(II) catalyzed oxidation of primary alcohols to aldehydes with atmospheric oxygen

Cyclometalation Reactions with Reaction Products of Amines and Aldehydes or Alcohols as Substrates

Decarboxylative Condensation, Aldehydes and Alcohols

Dehydrogenation of Alcohols to Aldehydes or Ketones

Dehydrogenations of alcohols to aldehydes

Formation of Alcohols, Aldehydes and Ketones

Hemiacetals formation from alcohols and aldehyde

Hemiacetals from alcohols + aldehydes

Hemiacetals from reaction of alcohols with aldehydes and ketones

Homoallylic alcohols from aldehydes

Hydroformylation, aldehydes from, with industrial alcohol syntheses

In oxidation of primary alcohols to aldehydes

Isopropyl alcohol, from acetone aldehydes

Ketones and aldehydes, distinguishing from reaction with alcohols to form acetal

Ketones and aldehydes, distinguishing from reaction with alcohols to form hemiacetal

Ketones or Aldehydes to Alcohols

OXIDATION OF PRIMARY ALCOHOLS AND ALDEHYDES

Of alcohols to aldehydes

Of benzylic alcohols to aldehydes

Oppenauer oxidation, aldehydes from, with alcohols

Oxazolidinones alcohol -> aldehyde -> carboxylic

Oxidation of Alcohols and Aldehydes

Oxidation of Alcohols and Aldehydes on Metal Catalysts

Oxidation of Alcohols to Aldehydes and Acids

Oxidation of Alcohols to Aldehydes, Ketones, and Carboxylic Acids

Oxidation of Alcohols to Aldehydes. Ketones, or Carboxylic Acids

Oxidation of Higher Alcohols and Aldehydes

Oxidation of alcohols and aldehydes to carboxylic acids

Oxidation of alcohols to aldehydes and ketones

Oxidation of alcohols to aldehydes or ketones

Oxidation, of primary alcohols to aldehydes

Oxidations of alcohols to aldehydes

Preparation of Aldehydes (Hydroformylation) and Alcohols

Primary Alcohols to Aldehydes (Table

Primary alcohol aldehyde reduction product

Primary alcohols aldehydes

Primary alcohols oxidation to aldehydes

Propionic aldehyde Propyl alcohols

Reaction Oxidation of a Primary Alcohol to an Aldehyde

Redox Rearrangement of Allylic Alcohols to Chiral Aldehydes

Reduction of Aldehydes and Ketones to Alcohols

Sakurai-Hosomi allylation, aldehydes homoallylic alcohols

Secondary alcohols compounds with aldehydes

Synthesis of Alcohols and Aldehydes

Synthesis of Aldehydes and Alcohols by the Oxo Reaction

The Reactions of Aldehydes and Ketones with Alcohols

Volatile alcohols, aldehydes, ketones

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