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1,4-Dichlorobenzene (1,4-DCB, p-DCB, or para-dichlorobenzene, sometimes abbreviated as PDCB or para) is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring.
A polymer is a substance composed of macromolecules. The latter usually have a range of molar masses (unit g mol −1), the distributions of which are indicated by dispersity (Đ). It is defined as the ratio of the mass-average molar mass (M m) to the number-average molar mass (M n) i.e. Đ = M m /M n. [4]
In short-term toxicity studies in animals, the typical effects are anorexia and wasting, and even after a huge dose animals die only 1 to 6 weeks after the TCDD administration. [36] Seemingly similar species have varying sensitivities to acute effects: lethal dose for a guinea pig is about 1 μg/kg, but to a hamster it is more than 1,000 μg/kg.
Rate 1 is the rate of effusion for the first gas. (volume or number of moles per unit time). Rate 2 is the rate of effusion for the second gas. M 1 is the molar mass of gas 1 M 2 is the molar mass of gas 2. Graham's law states that the rate of diffusion or of effusion of a gas is inversely proportional to the square root of its molecular weight.
1,2-Dichlorobenzene, or orthodichlorobenzene (ODCB), is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colourless liquid is poorly soluble in water but miscible with most organic solvents.
Once again, the molar volume is used to calculate the mass concentration, or mass density, but the reference fluid is a single component fluid, and the reduced density is independent of the relative molar mass. In mathematical terms this is
p-Xylene (para-xylene) is an aromatic hydrocarbon.It is one of the three isomers of dimethylbenzene known collectively as xylenes.The p-stands for para-, indicating that the two methyl groups in p-xylene occupy the diametrically opposite substituent positions 1 and 4.
Related salts are also known, such as 1-butylpyridinium chlorochromate, [C 5 H 5 N(C 4 H 9)][CrO 3 Cl] and potassium chlorochromate. PCC is commercially available. Discovered by accident , [ 3 ] the reagent was originally prepared via addition of pyridine into a cold solution of chromium trioxide in concentrated hydrochloric acid : [ 4 ]