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Bicyclo[1.1.0]butane is an organic compound with the formula C 4 H 6. It is a bicyclic molecule consisting of two cis -fused cyclopropane rings, and is a colorless and easily condensed gas. [ 1 ] Bicyclobutane is noted for being one of the most strained compounds that is isolatable on a large scale — its strain energy is estimated at 63.9 ...
2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials, usually as an alternative to bisphenol A (BPA).
The prefix consists of three numbers that are arranged in descending order, separated by dots: [2.2.1]. Before the numerical prefix is another prefix indicating the number of rings (e.g., "bicyclo+"). Thus, the name is bicyclo[2.2.1]heptane. Cycloalkanes as a group are also known as naphthenes, a term mainly used in the petroleum industry. [4]
The bridged bicyclic norbornane, formally bicyclo[2.2.1]heptane The spirocyclic compound spiro[5.5]undecane DABCO (1,4-diazabicyclo[2.2.2]octane) is often incorrectly depicted with one skewed ethylene group for the sake of clarity. A bicyclic molecule (from bi 'two' and cycle 'ring') is a molecule that features two joined rings. [1]
2,2,4,4-Tetramethylcyclobutanedione is the organic compound with the formula (CH 3) 4 C 4 O 2. The compound is a diketone of cyclobutane, bearing four methyl groups . It is a white solid that is used as a precursor to diverse industrial products.
2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol or tri-tert-butylcarbinol is an organic compound with formula C 13 H 28 O, ((H 3 C) 3 C) 3 COH, or t Bu 3 COH. [1] It is an alcohol that can be viewed as a structural analog of a tridecane isomer ( 2,2,4,4-tetramethyl-3- t -butylpentane ) where the central hydrogen has been replaced by a hydroxyl group ...
2 pb(c 2 h 5) 4 + 27 o 2 → 16 co 2 + 20 h 2 o + 2 pbo Pb and PbO would quickly over-accumulate and foul an engine. For this reason, 1,2-dichloroethane and 1,2-dibromoethane were also added to gasoline as lead scavengers—these agents form volatile lead(II) chloride and lead(II) bromide , respectively, which flush the lead from the engine and ...
2 and triethylborane generates the less substituted (and less stable) enolate. After reaction with methyl iodide the former mixture gives 2,2-dimethylcyclohexanone in 90% yield while the latter produces 2,6-dimethylcyclohexanone in 93% yield. [7] [8] The Et stands for ethyl group CH 3 CH 2 −.