Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aldehydes formaldehyde

Aldehydes. Formaldehyde, metaformaldehyde, acetaldehyde, paraldehyde, chloral hydrate, benzaldehyde, salicylaldehyde (and other substituted benzaldehydes). [Pg.316]

Figure 4.22 The Mannich reaction occurs between an active-hydrogen-containing compound (phenol) and an amine-containing molecule in the presence of an aldehyde (formaldehyde). The condensation reaction forms stable crosslinks. Figure 4.22 The Mannich reaction occurs between an active-hydrogen-containing compound (phenol) and an amine-containing molecule in the presence of an aldehyde (formaldehyde). The condensation reaction forms stable crosslinks.
Cyclohexane Methylcyclohexane Phenol Terpenes Turpentine Alcohols Methyl alcohol Ethyl alcohol 2-propen-l-ol n-Propyl alcohol Isopropyl alcohol n-Butyl alcohol Amyl alcohol Isoamyl alcohol Aldehydes Formaldehyde Acetaldehyde Acrolein... [Pg.567]

The Cannizzaro reaction is by no means confined to aromatic aldehydes. Formaldehyde undergoes the same change, yielding formic acid and methyl alcohol. That the aliphatic aldehydes from acetaldehyde upwards do not undergo the reaction is due to the fact that the aldol condensation (mentioned above), in virtue of its much greater velocity, takes precedence over the Cannizzaro reaction. [Pg.221]

Renzetti and Btyan measured total aldehydes, formaldehyde, and... [Pg.185]

The peroxyalkylnitrates and peroxyarylnitrates have been monitored by directly injecting the air at the sampling site into a specifically designed gas chromatograph. Aldehydes (formaldehyde is the major one in... [Pg.272]

Redox reaction between aromatic aldehydes, formaldehyde or other aliphatic aldehydes without a-hydrogen. Base is used to afford the corresponding alcohols and carboxylic acids. [Pg.107]

Nitrosamines (NDMA) Aldehydes (Formaldehyde) Ketones (Dimethy Igly oxal)... [Pg.97]

One way to create a carbon-carbon bond is to react a Grignard reagent with a carbonyl compound. The result of this reaction is an alcohol derived from an aldehyde. Formaldehyde gives a primary alcohol, but any other aldehyde gives a secondary alcohol. Ketones and esters both react to form tertiary alcohols. [Pg.251]

Epoxide Containing Compound Hydrolysis to 1,2-Dihydroxy Derivative Oxidation to Terminal Aldehyde Formaldehyde... [Pg.241]

Formaldehyde and acetaldehyde are the most common aldehydes. Formaldehyde is a gas at room temperature, so it is often stored and used as a 40% aqueous solution called formalin. When dry formaldehyde is needed, it can be generated by heating one of its solid derivatives, usually trioxane or paraformaldehyde. Trioxane is a cyclic trimer, containing three formaldehyde units. Paraformaldehyde is a linear polymer,... [Pg.821]

Suggest mechanisms for these two reactions of the smallest aldehyde, formaldehyde (methanal, CH2=0). [Pg.359]

At first sight formaldehyde (methanal, CH2=0) seems the ideal electrophilic partner in a mixed aldol reaction. It cannot enolize, (Usually we are concerned with oc hydrogen atoms in an aldehyde. Formaldehyde does not even have a carbon atoms.) And it is a super aldehyde. Aldehydes are more electrophilic than ketones because a hydrogen atom replaces one of the alkyl groups. Formaldehyde has two hydrogen atoms. [Pg.712]

The most important cotton etherification treatments are those that produce wrinkle resistance in fabrics [331,333,334]. The aldehydes, formaldehydes, and glyoxals, react with the OH groups of two cellulose chains as well as those of one chain. Reaction in which a bond is established between the two cellulose molecules is called cross-linking and is the basis for profound changes in the cotton fiber. Cross-linking produces resiliency in the fiber to give the needed dimensional stabilization, wrinkle resistance, and crease retention for modern durable-press cellulosic fabrics. Cross-links based on etherification reactions traditionally have been used because of their durability to repeated laundering and wear. [Pg.87]

The mechanism of the addition of HLi, CHsLi and their dimers to aldehydes (formaldehyde, acetaldehyde) has been studied by ab initio methods . For the thf cleavage. [Pg.25]

Iu the oils, beuzeue aud tolueue are the major compoueuts [11]. Beduas [39] fiuds aldehydes (formaldehyde aud acetaldehyde) as major compoueuts at 700°C. If the temperature rises 900°C, the amouut of acetaldehyde decreases aud carbou mouoxide becomes more importaut iu proportiou theu carbou dioxide [39]. This is explaiued by the decompositiou of acetaldehyde iu methaue aud carbou mouoxide. [Pg.266]

Oxidation of Aldehydes. Formaldehyde and acetaldehyde are major oxidation products of propylene that participate in smog reactions in... [Pg.31]

The capping of N3S3-semiclathrochelate [Co(ten)]3+ cation via a template-assisted mixed aldehyde (formaldehyde/propanal) condensation (Scheme 47) made it possible to obtain NsSs-sarcophaginates with both regular and contracted cavities in fairly high yield, as well as to isolate the corresponding free ligands [124]. [Pg.83]

Apart from the environmental factors, chemical compounds also induce cross-linking of gelatin. Supporting this is the mechanism in Fig. 5, which highlights the role of external aldehydes. Among the low molecular weight aldehydes, formaldehyde is most important as it is released in dosage forms from plasticizers and preservatives, fats, and polyethylenated... [Pg.1866]


See other pages where Aldehydes formaldehyde is mentioned: [Pg.469]    [Pg.2172]    [Pg.60]    [Pg.156]    [Pg.169]    [Pg.149]    [Pg.29]    [Pg.890]    [Pg.36]    [Pg.426]    [Pg.269]    [Pg.324]    [Pg.277]    [Pg.110]    [Pg.68]    [Pg.411]    [Pg.652]    [Pg.282]    [Pg.107]    [Pg.224]    [Pg.443]    [Pg.817]    [Pg.848]    [Pg.29]    [Pg.29]    [Pg.469]    [Pg.1928]    [Pg.166]    [Pg.591]    [Pg.193]    [Pg.632]   
See also in sourсe #XX -- [ Pg.311 ]




SEARCH



Aldehyde formaldehyde, derivatized

Aldehydes Crotonaldehyde Formaldehyde

Aldehydes reaction with formaldehyde

Estimation of Aldehydes (other than Formaldehyde)

Formaldehyde aromatic aldehydes

Hydroxy aldehydes from formaldehyde

© 2024 chempedia.info