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Chlorine chloro

Chlor-. of or combined with chlorine, chloro (as Chlorbenzoeadure, chlorobenzoic acid), chloride of (as Chlorzink, zinc chloride), chlorahnlich, a. like chlorine, chlorinous. Chlor-alaun, m. chloralum, -alkalien, n.pl. alkali-metal chlorides, -allyl, n, allyl chloride, -aluminium, n. aluminum chloride, -ammon, m., -ammonium, n. ammonium chloride, -amyl, n, amyl chloride, -antimon, n, antimony chloride, -arsenlk, n. chloride of arsenic, -arsenikldsung, /, (Pkarm.) solution of arsenious add, hydrochloric solution of arsenic, -arsinkampfstoff, m. chlorodi-phenylarsine, adamsite, chlorartig, a. like chlorine, chlorinous,... [Pg.90]

An alkyl halide is named as an alkane with a halogen substituent— that is, as a halo alkane. To name a halogen substituent, change the -ine ending of the name of the halogen to the suffix -o (chlorine chloro). [Pg.232]

Metallic derivatives frequently provide substrates for electrophilic chlorination. Chloro-demer-curation using sulfur monochloride gave a 65% yield of 5-chlorouracil <85CHE322, 88BAP499>. Similarly, ipso chlorination of 6-trimethylsilyl derivatives occurs on treatment with NCS <84TL3325, 93AHC(58)271>. [Pg.121]

Carbethoxylation Carboxylic acid-Carboxylic acids, branched Chlorine Chloro-... [Pg.365]

CH2CI-CO-CH3. Colourless lachrymatory liquid b.p. 119°C. Manufactured by treating propanone with bleaching powder or chlorine. It is used as a tear gas and is usually mixed with the more potent bromoacetone. chloro acids Complex chloroanions are formed by most elements of the periodic table by solution of oxides or chlorides in concentrated hydrochloric acid. Potassium salts are precipitated from solution when potassium chloride is added to a solution of the chloro acid, the free acids are generally unstable. [Pg.93]

MCPA, l-methyl-A-chlorophenoxyacetic acid, Methoxone, CgH ClOj. Made by chlorination of o-cresol followed by reaction with chloroethanoic acid. While crystals, m.p. 118-119 C. As usually obtained, crude MCPA contains both 4- (60%) and 6- (40%) chloro-isomers, and is a light brown solid. Selective weedkiller. [Pg.252]

The anhydrous chloride is prepared by standard methods. It is readily soluble in water to give a blue-green solution from which the blue hydrated salt CuClj. 2H2O can be crystallised here, two water molecules replace two of the planar chlorine ligands in the structure given above. Addition of dilute hydrochloric acid to copper(II) hydroxide or carbonate also gives a blue-green solution of the chloride CuClj but addition of concentrated hydrochloric acid (or any source of chloride ion) produces a yellow solution due to formation of chloro-copper(ll) complexes (see below). [Pg.410]

Dinitrophenylhydrazine is a very important reagent for the identification of aldehydes and ketones (pp. 342, 346). It is readily prepared from chloro-2,4-dinitrobenzene (I). In the latter compound the chlorine is very reactive in... [Pg.262]

The conversion of an aliphatic carboxylic acid into the a-bromo- (or a-chloro ) acid by treatment with bromine (or chlorine) in the presence of a catal3rtic amount of phosphorus tribromide (or trichloride) or of red phosphorus is known as the Hell-Volhard-Zelinsky reaction. The procedure probably involves the intermediate formation of the acyl halide, since it is known that halogens react more rapidly with acyl haUdes than with the acids themselves ... [Pg.427]

The substance is examined in a dilute solution in a solvent. A wide choice of solvents, transparent to ultraviolet radiation, is available. The paraffin hydrocarbons are all suitable, as are the ahphatic alcohols and the chlorinated hydrocarbons, such as chloroform and carbon tetrachloride. The most useful solvents are re-hexane, cycZohexane, chloro-... [Pg.1143]

Gr. chloros, greenish yellow) Discovered in 1774 by Scheele, who thought it contained oxygen. Chlorine was named in 1810 by Davy, who insisted it was an element. [Pg.41]

Treatment of a-thiocyanatoketones at low temperature with dry hydrogen chloride in ether solution gives satisfactory yields of 2-chloro-thiazole derivatives (188). The use of phosphorus pentachloride leads to the same results, but in this case chlorination can also occur at the 5-position (Scheme 97) (18, 68). [Pg.273]

FIGURE 4 2 Electro static potential maps of methanol and chloro methane The electrostatic potential is most negative near oxygen in methanol and near chlorine in chloromethane The most positive region is near the O—H proton in methanol and near the methyl group in chloromethane... [Pg.147]

Write the structures of the enol forms of 2 butanone that react with chlorine to give 1 chloro 2 butanone and 3 chloro 2 butanone... [Pg.758]

Rule 2. When atoms attached directly to a double-bonded carbon have the same priority, the second atoms are considered and so on, if necessary, working outward once again from the double bond or chiral center. For example, in l-chloro-2-methylbutene, in CH3 the second atoms are H, H, H and in CH2CH3 they are C, H, H. Since carbon has a higher atomic number than hydrogen, the ethyl group has the next highest priority after the chlorine atom. [Pg.45]

As part of the research described in Fig. 7.5, Winston and Wichacheewaf measured the percentages of carbon and chlorine in copolymers of styrene (molecule 1) and 1-chloro-l,3-butadiene (molecule 2) prepared from various feedstocks. A portion of their data is given below ... [Pg.498]


See other pages where Chlorine chloro is mentioned: [Pg.167]    [Pg.113]    [Pg.885]    [Pg.901]    [Pg.74]    [Pg.77]    [Pg.230]    [Pg.225]    [Pg.167]    [Pg.113]    [Pg.885]    [Pg.901]    [Pg.74]    [Pg.77]    [Pg.230]    [Pg.225]    [Pg.21]    [Pg.21]    [Pg.92]    [Pg.93]    [Pg.94]    [Pg.96]    [Pg.135]    [Pg.160]    [Pg.165]    [Pg.182]    [Pg.205]    [Pg.430]    [Pg.316]    [Pg.262]    [Pg.1057]    [Pg.153]    [Pg.176]    [Pg.502]    [Pg.534]    [Pg.535]    [Pg.31]    [Pg.476]   
See also in sourсe #XX -- [ Pg.93 ]

See also in sourсe #XX -- [ Pg.93 ]




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2- Chloro-6-hydroxy pyrazine chlorination

2-Chloro-3-methylpyrazine chlorination

2-Chloro-5-hydroxypyrazine chlorination

Pyruvic acid, chlorination to chloro

Quinoxaline a-chloro-, displacement of chlorine

Sulfides, a-chloro via sulfide chlorination

Varying Si-Chlorinated 2-Methyl-2-chloro-l,3-disilapropanes

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