Acetyl chloride Acrolein

Acetic Acid Acetic anhydride Acetoacetanilide Acetone cyanhydnn Acetyl chloride Acrolein Acrylonitrile Alcohols Alkaloids... 

Acetyl chloride, see 1.1.1-Trichloroethane Acetyl-CoA, see Cyclohexane Acetylene, see Benzene. Ethylenimine, Hexachloroethane, TCDD Acrolein, see Acrylonitrile, Allyl alcohol, Atrazine. Acrylamide, see Acrylonitrile Acrylic acid, see Acrylamide, Ethyl acrylate. Methyl acrylate... 

Problem 15.50 Show steps in the following syntheses (a) acetyl chloride to acetal (CH,CH(OC,H,)j), (b) allyl chloride to acrolein (propenal), (c) ethanol to 2-butene. ... 

Ethylenediamine-bisborane is a white crystalline solid which is quite stable on standing and can be stored at room temperature in a desiccator for several months. It evolves hydrogen slowly on warming and decomposes rapidly at about 90°C. The use of this compound for the reduction of acetone, acrolein, cinnamaldehyde, and acetyl chloride to the corresponding alcohols (isopropyl alcohol, allyl alcohol, cinnamyl alcohol, and ethyl alcohol) has been described.1 Its solubility characteristics and its thermal and hydrolytic stability have been reported.1-4... 

Acetyl chloride acephate, azaconazole, chlorfenvinphos, cyhalotrin, dimethomorph, dinoseb acetate, fenitropan, fluxofenim, furconazole, mefluidide, propiconazole Acetyl chloride (dichloro) see dichloro Acetyl chloride phenyl carbinol bromadiolone Acetylene aldrin, 2,4 DB Acetyl hydrazine metamitron Acetylide (sodium) pronamide Acetyl magnesiun bromide empenthrin Acetyl morpholine dimethomorph Acetyloxy propionaldehyde furmecyclox Acrolein 8 hydroxy quinoline sulfate Acrylic acid propaquizafop Acryloyl chloride propaquizafop Acrylonitrile fenpiclonil, fludioxonil, nipyraclofen Aldrin dieldrin, endrin... 

Mixed vapors of acrolein and ethyl alcohol were passed over the catalyst in a heated stainless steel tube at atmospheric pressure. Products were condensed and fractionated in a 20-plate bubble tray column. Fractions taken were acetaldehyde, 20-36°, and acrolein-ethyl alcohol, 36-78.4°. At this point water was added to the distillation kettle and an ethyl alcohol-aUyl alcohol-water fraction, 78-95°, was taken overhead. Fractions were analyzed for aldehydes by the hydroxylamine hydrochloride method, for im-saturation by reaction with bromine in aqueous potassium bromide, for alcohol by the nitrite ester method, and for water with Fischer reagent. Propyl alcohol in the water-free allyl alcohol recovered from the azeotrope was calculated by difference from the total alcohol determined by reaction with acetyl chloride and the unsaturated alcohol determined by reaction with aqueous bromine solution. Fresh catalyst was used for each experiment. 

Acrolein Acetyl chloride Acetylene-arsenic trichloride Acetyl fluoride Aluminum chloride Aluminum arsenide Ammonium cyanide... 

Trivial name Acetaldehyde Acetamide Acetic acid Acetic anhydride Acetoacetic acid Acetone Acetonitrile Acetophenone Acetyl chloride Acetylene Acrolein Acrylamide Acrylic acid Acrylonitrile Adipic acid Amyl acetate Amyl alcohol tert-Amy alcohol Aniline Azelaic acid Benzoic acid Benzoyl peroxide Benzyl alcohol Bisphenol A... 

Acetyl-d-mcthyl-5-phcnyi-1,3-oxaro idinc-2-lhione, 4 3-Acely]>2-oxazoUdonc. 351 (o-Acetylphenoxy)phenylacetyl chloride, 5 Acrolein, 7. 193, 348... 

Dihydropyran derivatives were synthesized as follows 2-(tosyloxymethyl)-3,4-dihydro-2H-pyran was prepared by the reaction of tosyl chloride with 2-(hydroxymethyl)-3,4-dihydro-2H-pyran, which was obtained by reduction of 2-formyl-3,4-dihydro-2H-pyran, Diels-Alder product of acrolein, with the aid of NaBH4. Syntheses of 2-(nucleic acid base methyl)-3,4-dihydro-2H-pyrans were achieved by treatment of sodium salts of the corresponding nucleic acid bases with 2-(tosyloxymethyl)-3,4-dihydro-2H-pyran in dimethylformamide. In order to facilitate its copolymerization with maleic anhydride, the amino group of adenine was blocked by acetyl group. 

Epichlorohydrin, 6—CihCH—CH2CI, can be obtained by the oxidation of allyl chloride with peracids, by the high-temperature chlorination of propylene with subsequent addition of chlorine/water and elimination of hydrogen chloride, or by a three-stage process starting with acrolein. Elastomers resistant to oil, ozone, and cold can be obtained from the homopolymerization of epichlorohydrin with, for example, Et3Al/H20/acetyl acetone as initiator ... 

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