![India rubber world. ning alundum,and after the acetone and the ethyl acetate have been expelledby warming the boat for several hours in the drying oventhe nitrosite is burned in a current India rubber world. ning alundum,and after the acetone and the ethyl acetate have been expelledby warming the boat for several hours in the drying oventhe nitrosite is burned in a current](https://c8.alamy.com/comp/2CEG0H5/india-rubber-world-ning-alundumand-after-the-acetone-and-the-ethyl-acetate-have-been-expelledby-warming-the-boat-for-several-hours-in-the-drying-oventhe-nitrosite-is-burned-in-a-current-of-oxygen-and-the-carbondioxide-formed-is-absorbed-in-soda-lime-and-weighed-the-method-proposed-is-to-grind-a-sample-to-20-mesh-ifpossible-and-weigh-out-vz-gram-and-extract-with-acetone-in-awiley-or-cottle-extractor-transfer-to-a-50-cc-flask-anddissolve-or-swell-in-40-cc-of-chloroform-nitrogen-trioxideis-made-from-arsenic-trioxide-with-13-sp-gr-nitric-acid-andthis-is-passed-through-the-rubber-so-2CEG0H5.jpg)
India rubber world. ning alundum,and after the acetone and the ethyl acetate have been expelledby warming the boat for several hours in the drying oventhe nitrosite is burned in a current
![Diluente Nitro Antinebbia Lt.25 UN1993, Liquido infiammabile N.A.S. (Acetone; N-eptano),3, II (D/E) Pericoloso per l'ambiente – Gst Italia Diluente Nitro Antinebbia Lt.25 UN1993, Liquido infiammabile N.A.S. (Acetone; N-eptano),3, II (D/E) Pericoloso per l'ambiente – Gst Italia](https://www.gst-italia.com/wp-content/uploads/2021/12/Kem-DNAEK0025-000-3861.jpg)
Diluente Nitro Antinebbia Lt.25 UN1993, Liquido infiammabile N.A.S. (Acetone; N-eptano),3, II (D/E) Pericoloso per l'ambiente – Gst Italia
![Figure 2 | Synthesis and Conformational Assignment of N-(E)-Stilbenyloxymethylenecarbonyl-Substituted Hydrazones of Acetone and o-(m- and p-) Chloro- (nitro-) benzaldehydes by Means of and NMR Spectroscopy Figure 2 | Synthesis and Conformational Assignment of N-(E)-Stilbenyloxymethylenecarbonyl-Substituted Hydrazones of Acetone and o-(m- and p-) Chloro- (nitro-) benzaldehydes by Means of and NMR Spectroscopy](https://static.hindawi.com/articles/jspec/volume-2013/197475/figures/197475.fig.002.jpg)
Figure 2 | Synthesis and Conformational Assignment of N-(E)-Stilbenyloxymethylenecarbonyl-Substituted Hydrazones of Acetone and o-(m- and p-) Chloro- (nitro-) benzaldehydes by Means of and NMR Spectroscopy
![Synthesis of 4-Hydroxy-4-(4-nitrophenyl)butan-2-one using p-Nitro Benzaldehyde and Acetone in Aqueous Micellar Media using L-Proline | Semantic Scholar Synthesis of 4-Hydroxy-4-(4-nitrophenyl)butan-2-one using p-Nitro Benzaldehyde and Acetone in Aqueous Micellar Media using L-Proline | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/fb3525c5cdbe6f070e4892f4cb2b282dcdced579/2-Figure1-1.png)
Synthesis of 4-Hydroxy-4-(4-nitrophenyl)butan-2-one using p-Nitro Benzaldehyde and Acetone in Aqueous Micellar Media using L-Proline | Semantic Scholar
![Mechanism and rate constant of proline-catalysed asymmetric aldol reaction of acetone and p-nitrobenzaldehyde in solution medium: Density-functional theory computation - ScienceDirect Mechanism and rate constant of proline-catalysed asymmetric aldol reaction of acetone and p-nitrobenzaldehyde in solution medium: Density-functional theory computation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2090123218300365-fx1.jpg)