Related Experiment Video
Updated: May 1, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Selective oxidation of cyclohexane using Ce1-xMnxO2 nanocatalysts
Abstract:
The Ce1-xMnxO2 nanocatalysts (x = 0.25, 0.50 and 0.75 wt.%) were synthesized by sol-gel method. The catalysts were characterized using various techniques such as XRD, N2 sorption study, DRSUV-Vis, TPR, SEM and TEM. The incorporation of Mn ions into the ceria lattice was confirmed by XRD analysis. DRUV-Vis spectra confirm the presence of Ce3+ ions in the lattice of Ce1-xMnxO2. H2-TPR study revealed the oxygen storage capacity of the catalyst. The 3D flowerlike morphology of the nanocatalysts was confirmed from FESEM and HRTEM images. The catalytic activity was tested for the vapor phase oxidation of cyclohexane using air as an oxidant. The key reaction parameters were varied to study the stability, activity and selectivity of the catalysts. The study concluded that suitable amount of manganese content is essential for the selective oxidation of cyclohexane at low temperature and Ce0.25Mn0.75O2 is the most suitable catalyst for high conversion and selectivity under the given reaction conditions. The activity of the catalyst is correlated with the characterization results.
Related Concept Videos
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy...
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

