And the conversion of benzaldehyde increased with the elevation of sulfonation temperature. This reaction is known as nitration of benzene. No formation of the product was observed inthepresenceofonlyA1orDABCO(Table 1,entry 3).Hou and co-workerspreviously observed the generation of sulfinic anions from tosylimines under NHC catalysis. Because three of them place a positive charge on a carbon atom … 14 • In Friedel-Crafts alkylation, treatment of benzene with an alkyl halide and a Lewis acid (AlCl3) forms an alkyl benzene. Benzaldehyde can be oxidized to benzoic acid; in fact "[B]enzaldehyde readily undergoes autoxidation to form benzoic acid on exposure to air at room temperature"[16] causing a common impurity in laboratory samples. Benzaldehyde has been used as a standard in the quantification of Achillea ligustica essential oil by GC-MS (Gas Chromatography-Mass Spectrometry). [22] Benzaldehyde does not accumulate in human tissues. Removal of a proton from carbocation intermediate. Reaction of benzaldehyde with anhydrous sodium acetate and acetic anhydride yields cinnamic acid, while alcoholic potassium cyanide can be used to catalyze the condensation of benzaldehyde to benzoin. Via aldol condensations, benzaldehyde is converted into derivatives of cinnamaldehyde and styrene. Benzaldehyde may be used in the following studies:• Preparation of optically active 1-phenylpropan-1-ol. This protocol works well for aldehydes including aromatic and aliphatic aldehydes. In some cases, a COA may not be available on-line. 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