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4-tert-Butylbenzaldehyde is notable as a rare example of industrial-scale electrochemistry. It is produced by BASF and Givaudan (typically as its methanol acetal) through a double anodic oxidation of 4-tert-butyltoluene on greater than 10,000 ton per year scale. [2] [3]
Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...
Diacetylene (also known as butadiyne) is the organic compound with the formula C 4 H 2. It is the simplest compound containing two triple bonds . It is first in the series of polyynes , which are of theoretical but not of practical interest.
CAS Number. 4748-78-1 ... C 9 H 10 O: Molar mass: 134.178 g·mol −1 Appearance clear colourless to slightly yellow liquid Density: 1.001 g/mL
[2] [3] [4] The aldol reaction is paradigmatic in organic chemistry and one of the most common means of forming carbon–carbon bonds in organic chemistry . [ 5 ] [ 6 ] [ 7 ] It lends its name to the family of aldol reactions and similar techniques analyze a whole family of carbonyl α-substitution reactions , as well as the diketone ...
C 6 H 6 + C 2 H 4 → C 6 H 5 C 2 H 5. The diethylbenzene is an inadvertent side product. C 6 H 5 C 2 H 5 + C 2 H 4 → C 6 H 4 (C 2 H 5) 2. Using shape-selective zeolite catalysts, the para isomer can be produced in high selectivity. Much diethylbenzene is recycled by transalkylation to give ethylbenzene: [1] C 6 H 4 (C 2 H 5) 2 + C 6 H 6 → ...
The Tishchenko reaction is an organic chemical reaction that involves disproportionation of an aldehyde in the presence of an alkoxide.The reaction is named after Russian organic chemist Vyacheslav Tishchenko, who discovered that aluminium alkoxides are effective catalysts for the reaction.
Aminoacetaldehyde is the organic compound with the formula OHCCH 2 NH 2.Under the usual laboratory conditions, it is unstable, tending instead to undergo self-condensation. [1]