The Absolute Best Science Experiment for 2144-40-3

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 2144-40-3. In my other articles, you can also check out more blogs about 2144-40-3

Synthetic Route of 2144-40-3, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 2144-40-3, Name is (cis-Tetrahydrofuran-2,5-diyl)dimethanol, molecular formula is C6H12O3. In a Article£¬once mentioned of 2144-40-3

Switchable synthesis of 2,5-dimethylfuran and 2,5-dihydroxymethyltetrahydrofuran from 5-hydroxymethylfurfural over Raney Ni catalyst

Raney-type metals (Cu, Co and Ni) were employed to catalyze hydrogenation of 5-hydroxymethylfurfural. Switchable synthesis of 2,5-dimethylfuran and 2,5-dihydroxymethyltetrahydrofuran was achieved with 96% and 88.5% yield respectively over Raney Ni, demonstrating high feasibility for industrialization. The excellent yields can be explained by the fact that Raney Ni facilitates the hydrogenation reaction but has limited deoxygenation ability at low temperature, while high temperature promotes the deoxygenation step. The reaction pathway was analyzed by time course experiments and HMF hydrogenation over model catalysts was performed. The reaction mechanism related to the respective catalytic sites was discussed and proposed, which has great implications in the design of efficient and non-noble metal catalysts.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 2144-40-3. In my other articles, you can also check out more blogs about 2144-40-3

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem