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Dichlorobenzenes

Production of o-dichlorobenzene is around 80,000 tpa. The largest producers are the United States, Japan and West Germany. [Pg.229]

Another herbicide based on 3,4-dichloroaniline, produced in similar quantities, is diuron Du Pont), which can be obtained by the reaction of 3,4-dichloroaniline, urea and dimethylamine accompanied by the liberation of ammonia. [Pg.230]

4-Dichloroaniline and propionic acid react together in the presence of thionyl chloride to yield propanil, a herbicide introduced by Rohm Haas. [Pg.230]

The reaction of 3,4-dichloronitrobenzene with KF in aprotic solvents such as sulfolane gives 3-chloro-4-fluoronitrobenzene, which is converted into the Shell herbicide flamprop-methyl by reduction, reaction with chloropropionic acid, esterification and subsequent acylation with benzoyl chloride. [Pg.230]

Polyphenylene sulfide is used in the manufacture of thermoplastic resins, which are marked by high long-term temperature stability (260 °C) and good chemical resistance (Phillips Petroleum, USA Kureha, Japan). [Pg.231]


Two other types of equilibrium curves are occasionally encountered with the system of two components forming a continuous series of solid solutions. These are shown in Figs. 1,16, 3 and 1,16, 4. In the former the freezing or melting curve passes through a minimum (examples p-chloroiodobenzene, m.p. 57° - p-dichlorobenzene, m.p. 53° naphtha-... [Pg.34]

The observation of nitration in nitromethane fully dependent on the first power of the concentration of aromatic was made later. The rate of reaction of /)-dichlorobenzene ([aromatic] = 0-2 mol [HNO3] = 8-5 mol 1 ) obeyed such a law. The fact that in a similar solution 1,2,4-trichlorobenzene underwent reaction according to the same kinetic law, but about ten times slower, shows that under first-order conditions the rate of reaction depends on the reactivity of the compound. [Pg.33]

In acetic acid the rates of nitration of chlorobenzene and bromo-benzene were fairly close to being first order in the concentration of aromatic, and nitration fully according to a first-order law was observed with O, m-, and/i-dichlorobenzene, ethyl benzoate and 1,2,4-trichloro-benzene. [Pg.35]

Using the partial rate factors for nitration of chlorobenzene, Ridd and de la Mare calculated the relative rates of nitration of the dichlorobenzenes, with respect to /)-dichlorobenzene, with the results shown below. Also given are results based on more recent nitrations in mixed... [Pg.187]

Which one of the dichlorobenzene isomers does not have a dipole moment" Which one has the largest dipole moment" Compare your answers with the dipole moments calculated using the molecular modeling software in Learning By Modeling... [Pg.472]

From among the compounds chlorobenzene o dichlorobenzene and p dichlorobenzene choose the one that... [Pg.580]


See other pages where Dichlorobenzenes is mentioned: [Pg.134]    [Pg.134]    [Pg.134]    [Pg.134]    [Pg.134]    [Pg.545]    [Pg.546]    [Pg.546]    [Pg.41]    [Pg.41]    [Pg.179]    [Pg.179]    [Pg.187]    [Pg.187]    [Pg.212]    [Pg.216]    [Pg.211]    [Pg.433]    [Pg.503]    [Pg.570]    [Pg.570]    [Pg.570]    [Pg.286]    [Pg.286]    [Pg.286]    [Pg.402]    [Pg.402]    [Pg.402]    [Pg.424]    [Pg.452]    [Pg.452]    [Pg.452]    [Pg.471]    [Pg.471]    [Pg.471]    [Pg.500]    [Pg.518]    [Pg.518]    [Pg.518]    [Pg.547]    [Pg.547]    [Pg.547]    [Pg.590]   
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1.2- dichlorobenzene

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