A propane tank perched on concrete blocks looked out of place in the antiquated setting.
The cis 1.2-cyclo-propane dicarboxylic acid is formed by eliminating carbon dioxide from cyclo-propane tricarboxylic acid -1.2.3 (from 43-dibrompropionic ester and sodio-malonic ester).
Soc., 1891, 59, p. 79 8); by the action of trimethylene bromide on disodio-propane tetracarboxylic ester; and by the reduction of isophthalic acid with sodium amalgam, the tetrahydro acids first formed being converted into hydrobromides and further reduced (A.
Propane, CH 3 CH 2 CH 3, can give rise to two alcohols - a primary alcohol, CH 3 CH 2 CH 2 OH (normal propyl alcohol), formed by replacing a hydrogen atom attached to a terminal carbon atom, and a secondary alcohol, CH 3.
Thus ethane gives H3C CH2 CH3, propane; ethylene gives H 2 C:CH CH 3, propylene; and acetylene gives HC: C CH 3, allylene.
Equally well we may derive it from methane by replacing a hydrogen atom by the monovalent group CH 2 CH 31 named ethyl; hence propane may be considered as " ethylmethane."
In propane, on the other hand, the hydrogen atoms attached to the terminal carbon atoms differ from those joined to the medial atom; we may therefore expect to obtain different compounds according to the position of the hydrogen atom substituted.
The identity of the four valencies of the carbon atom follows from the fact that the heats of combustion of methane, ethane, propane, trimethyl methane, and tetramethyl methane, have a constant difference in the order given, viz.
In the difference between C - C - C - C C-C-C and With this compound C 4 H 10, named butane, C isomerism is actually observed, being limited to a pair, whereas the former members ethane, C 2 H 6, and propane, C 3 H 8, showed no isomerism.
POLYMETHYLENES, in chemistry, cyclic compounds, the simplest members of which are saturated hydrocarbons of general formula C 7, H 2nj where n may be r to 9, and known as tri-, tetra-, penta-, hexa-, and hepta-methylene, &c., or cyclo- propane, -butane, -pentane, -hexane, -heptane, &c.: - CH 21 CH 2 CH 2 CH2.CH2 CH2 CH2 CH2?C1H,, I I H ?
Cyclo-propane, -butane, -pentane, -hexane.
C02R CH 3 CH: CBr CO 2 R+NaCH (CO 2 R) 2 --->CH 3 C. I C(C02R)2 by the action of diazomethane or diazoacetic ester on the esters of unsaturated acids, the pyrazoline carboxylic esters so formed losing nitrogen when heated and yielding acids of the cyclo- propane series (E.
Cyclo-propane Group. Trimethylene, Calls, obtained by A.
Cyclo-propane carboxylic acid, C 3 H 5 CO 2 H, is prepared by heating the 1.1- dicarboxylic acid; and by the hydrolysis of its nitrile, formed by heating y-chlorbutyro-nitrile with potash (L.