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Developed in the Philippines, this method (abbreviated HPSD) consists of a cylinder pressure cap made from a 3 mm thick mild steel plate secured with 8 sets of bolts, a 2-HP diesel engine, and a pressure regulator with 1.4–14 kg/m 2 capacity. The cap is placed over the stump of a pole, tree or bamboo and the preservative is forced into the ...
Structures of the three isomers of tolyl group. In organic chemistry, tolyl groups are functional groups related to toluene. [1] They have the general formula CH 3 C 6 H 4 −R, the change of the relative position of the methyl and the R substituent on the aromatic ring can generate three possible structural isomers 1,2 (ortho), 1,3 (meta), and 1,4 (para).
CH 3 OC 6 H 5 + (CH 3 CO) 2 O → CH 3 OC 6 H 4 C(O)CH 3 + CH 3 CO 2 H. Unlike most acetophenones, but reflecting the influence of the methoxy group, methoxyacetophenone undergoes a second acetylation. Many related reactions have been demonstrated. For example, phosphorus pentasulfide (P 4 S 10) converts anisole to Lawesson's reagent, [(CH 3 OC ...
Pages in category "4-Tolyl compounds" The following 25 pages are in this category, out of 25 total. This list may not reflect recent changes. A. Acrivastine; B.
This process is similar to the Les Bois Perdure treatment in that it uses a steam environment at atmospheric pressure to treat the wood. However, this process can also be used on "green" wood and was the most widely used commercial process as of 2004. [5] [10] Genuine industrial scale ThermoWood process was developed in Finland in 1990's.
The mixture is infused into wood at high pressure. [4] In the treated wood, arsenic is believed to be in the form of chromium (III) arsenate CrAsO 4 and/or copper(II) arsenate Cu 3 (AsO 4) 2, or fairly stable chromium dimer-arsenic clusters. [4]
ch 3 c 6 h 4 so 3 h + 2 naoh → ch 3 c 6 h 4 oh + na 2 so 3 + h 2 o Other methods for the production of p -cresol include chlorination of toluene followed by hydrolysis. In the cymene-cresol process, toluene is alkylated with propene to give p -cymene , which can be oxidatively dealkylated in a manner similar to the cumene process .
In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3. It consists of a tolyl group, −C 6 H 4 −CH 3, joined to a sulfonyl group, −SO 2 −, with the open valence on sulfur. This group is usually derived from the ...