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Alcohols acetals

Hydroperoxides have been obtained from the autoxidation of alkanes, aralkanes, alkenes, ketones, enols, hydrazones, aromatic amines, amides, ethers, acetals, alcohols, and organomineral compounds, eg, Grignard reagents (10,45). In autoxidations involving hydrazones, double-bond migration occurs with the formation of hydroperoxy—azo compounds via free-radical chain processes (10,59) (eq. 20). [Pg.105]

Sap. Figure. Acetate. Alcohol. Alcohol in the Orig. Oil. Acetate. Alcohol. Alcohol in the Orig, Oil. Sap. Figure. [Pg.323]

Not all modified starches are suitable for removal by aqueous dissolution alone. Such modifications of natural starches are carried out to reduce solution viscosity, to improve adhesion and ostensibly to enhance aqueous solubility. Commercial brands vary [169], however, from readily soluble types to those of limited solubility. Indeed, some may be as difficult to dissolve as potato starch if they have been overdried. It is thus very important to be sure of the properties of any modified starch present. If there are any doubts about aqueous dissolution, desizing should be carried out by enzymatic or oxidative treatment. Even if the size polymer is sufficiently soluble, it is important to ensure that the washing-off range is adequate. Whilst the above comments relate to modified starches, other size polymers such as poly(vinyl acetate/alcohol) and acrylic acid copolymers vary from brand to brand with regard to ease of dissolution. [Pg.105]

Poly (vinyl acetate/alcohol) sizes are also described as water-soluble and are widely used, either alone or in combination with most of the other types, across the whole range of fibres and blends [169,171]. However, this category covers a wide range of commercial products, differing greatly in quality and ease of removal. Indeed, some are quite difficult to remove, thus necessitating careful selection [187]. Detailed studies of factors affecting the removal of water-soluble sizes, particularly poly(vinyl alcohol) types, have been published [188-190]. [Pg.106]

It is likely that the spectrum of compounds produced by all Mastophora species includes a wider range of compounds than those found in this study. Several Mastophora species catch male moths that are known to respond to pheromone compounds in the even-carbon number aldehyde/ acetate/alcohol chemical class, as well as males of other species that are known to respond to pheromone compounds in the odd-carbon number hydrocarbon chemical class (9, 13). [Pg.70]

FIGURE 3 Pheromone biosynthetic pathways commonly used in moth sex pheromone glands to produce precursors for specific blends of acetates, alcohols, or aldehydes. Cascades of precursors are produced by combinations of unique A- -desaturases and limited chain-shortening steps. The six precursors for the cabbage looper blend (Figure 2) are in boldface type. [Pg.118]

The sex pheromones of moths generally are mixtures of two or more chemical components, typically aldehydes, acetates, alcohols, or hydrocarbons, produced in specialized glands by biosynthesis and modification of fatty acids (34). Often, a species-specific blend of components is the message, and males of many moth species, including M. sexta, give their characteristic, qualitatively and quantitatively optimal behavioral responses only when stimulated by the correct blend of sex-pheromone components and not by individual components or partial blends lacking key components (43, 44). [Pg.179]

Man-made binders Bakelite resin, polyester resin, chlorinated rubber, polyvinyl chloride, Thiokol rubber, epoxy resin, Thiokol-epoxy blends, vinyl acetate alcohol resin (VAAR), Viton-A, Teflon and Kel-F800 etc. [Pg.335]

Vinyl Acetate Alcohol Resins These may be considered as a vinyl acetate/vinyl alcohol copolymers consisting of 82% vinyl acetate and 18% vinyl alcohol and is supplied as a solid dissolved in methyl alcohol (18%) and methyl acetate (82%) or technical grade methyl acetate. It is popularly known as VAAR. Military specification MIL-V-50433 (MU), July 1969 governs the quality of its solution for use in ammunition. [Pg.352]

Scheme 5.1 Synthesis of vinyl acetate alcohol resin (VAAR). Scheme 5.1 Synthesis of vinyl acetate alcohol resin (VAAR).
Two general classes of pheromone compound have been identified in moths, and these have some broad, although not uniform, associations with certain taxa. The polyene hydrocarbons and epoxides of various chain lengths are pheromones found in some subfamilies of the Geometridae and Noctuidae, and in the Arctiidae and Lymantridae (Millar, 2000). These compounds are probably derived from dietary Unoleic and linolenic acids. The other major class of pheromone compounds includes acetate, alcohols, and aldehydes, which are found in the Tortrici-dae, Pyralidae, Gelechiidae, Sessiidae, and Noctuidae. This class of compounds is derived from the insect s fatty acid synthesis pathway, with enzymatic modifications discussed above. Both classes of pheromone are broadly represented in the Noctuidae but are typically found in different subfamilies (Am et al., 1992,2003). [Pg.297]

Fig. 8.4. Proportions of male Hemileuca eglanterina attracted to lures baited with either 100 10 1 (white area) or 0 100 10 (black area) acetate-alcohol-aldehyde blends at various locations along the eastern slope of the Sierra Nevada Mountains. (From McElfresh and Millar (2001), where designations for localities can be found.)... Fig. 8.4. Proportions of male Hemileuca eglanterina attracted to lures baited with either 100 10 1 (white area) or 0 100 10 (black area) acetate-alcohol-aldehyde blends at various locations along the eastern slope of the Sierra Nevada Mountains. (From McElfresh and Millar (2001), where designations for localities can be found.)...
When the Pd bears chiral ligands, these reactions can be enantioselective.1448 ir-Allylmo-lybdenum compounds behave similarly.1449 Because palladium compounds are expensive, a catalytic synthesis, which uses much smaller amounts of the complex, was developed. That is, a substrate such as an allylic acetate, alcohol, amine, or nitro compound1450 is treated with the nucleophile, and a catalytic amount of a palladium salt is added. The rr-allylpal-ladium complex is generated in situ. Alkene-palladium complexes (introducing the nucleophile at a vinylic rather than an allylic carbon) can also be used.1451... [Pg.468]

Dinitrochloroiodomethane, (02N)2C.I(C1) mw 2.66.38, N 10.5 2% col oil, having characteristic odor of halogenonitroparaffins, slowly becomes reddish-brn on standing, dec on heating, d 2.14 24 at 12° was prepd by passing chlorine into an ice-cold aq soln of dinitroiodomethane Na acetate. Alcoholic KOH converts this compd into a mixt of expl salts, K chloro- ... [Pg.42]

Small simple cooling systems may be treated with amines in the form of slowly dissolving waxy blocks that can be suspended in baskets, whereas larger or more difficult systems use liquid products containing diamine acetates/alcohols. [Pg.149]

Ternary acetate-alcohol-water systems (propyl, butyl, amyl, hexyl) 178 Azeotrope problem ... [Pg.288]


See other pages where Alcohols acetals is mentioned: [Pg.855]    [Pg.493]    [Pg.71]    [Pg.855]    [Pg.337]    [Pg.672]    [Pg.691]    [Pg.100]    [Pg.105]    [Pg.35]    [Pg.352]    [Pg.357]    [Pg.60]    [Pg.320]    [Pg.109]    [Pg.113]    [Pg.289]    [Pg.1]    [Pg.70]    [Pg.18]    [Pg.862]    [Pg.1192]    [Pg.1592]    [Pg.135]    [Pg.184]   
See also in sourсe #XX -- [ Pg.258 , Pg.259 , Pg.260 , Pg.261 ]




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3- Phenylpropanal, from allyl alcohol and phenylpalladium acetate

Acetal formation alcohols protection

Acetals alcohol protection

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

Acetals from alcohols

Acetals from enol ethers + alcohols

Acetate Alcohol Resins

Acetate alcohol resins, vinyl

Acetates alcohol protection

Acetic acid alcohols, order

Acetic acid bacteria alcohol fermentation

Acetic acid esterification reaction with alcohols

Acetic acid from ethyl alcohol

Acetic acid with alcohols

Acetic anhydride DMSO oxidation of alcohols

Acetic anhydride with alcohols

Acetic anhydride, electrostatic reaction with alcohols

Acetic anhydride, trifluoroactivator DMSO oxidation of alcohols

Acetylations alcohols, acetic anhydride

Acids acetic from alcohol

Addition of Alcohols to Form Hemiacetals and Acetals

Addition of Alcohols—Acetal Formation

Addition of alcohols hemiacetal and acetal formation

Alcohol acetal formation

Alcohol acetates production

Alcoholic fermentation acetic acid

Alcoholic hydroxyl acetal derivatives

Alcohols acetate protecting groups

Alcohols acetate synthetic equivalent

Alcohols acetates

Alcohols acetates

Alcohols acetylation with acetic anhydrid

Alcohols estimation with acetic anhydride

Alcohols palladium®) acetate

Alcohols zinc-acetic acid

Alcohols, Ethers, and Acetals

Alkenes allylic alcohols, palladium acetate

Allyl acetates via alcohols

Amyl acetate alcohol

Benzyl acetate alcohol

Benzyl alcohol 2,4,6-trimethyl-, acetate

Butyl acetate alcohol

Butyl acetate alcohol tertiary

Butyl acetate alcohol, tert

Carbonyl compounds alcohol oxidations, palladium acetate

Cupric acetate alcohols

Esterification of alcohol with acetic anhydride using a fluorous scandium catalyst

Ethyl acetate alcohol

Ethyl acetate from acetic acid and alcohol

Ethyl acetate methyl alcohol

Hexyl alcohol, acetate

Isobutyl acetate alcohol

Isopropyl acetate alcohol

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

Lead acetate, alcohol oxidations, pyridine

Mercuric Acetate allyl alcohol with

Methyl acetate alcohol

Nucleophilic Addition of Alcohols Acetal Formation

Octyl acetate alcohol

Phenylethyl acetate alcohol

Polyvinyl alcohol acetate

Primary alcohol oxidations acetic anhydride

Propyl acetate alcohol

Protection of Alcohols by Acetal Formation

Protonated acetic alcohol

R-Butyl alcohol via ethyl acetate

Reaction benzyl alcohol with acetic acid

Reaction with Alcohols Acetals and Ketals

Recovery of Methanol and Acetic Acid in Poly (Vinyl Alcohol) Production

Secondary alcohols acetic anhydride

The Addition of Alcohols Hemiacetals and Acetals

VAAR (vinyl acetate alcohol resins

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