Related Experiment Video
Updated: Apr 5, 2026

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
Published on: February 7, 2017
Controlling tunnelling in methane loss from acetone ions by deuteration
Andras Bodi1, Tomas Baer2, Nancy K Wells3
1Molecular Dynamics Group, Paul Scherrer Institute, Villigen 5232, Switzerland. andras.boedi@psi.ch.
Abstract:
Energetic acetone cations decay by methane or methyl radical loss. Although the methane-loss barrier to form the ketene cation is higher and the activation entropy is lower, it has a significant branching ratio at low energies thanks to quantum tunnelling. H-atom tunnelling can be selectively quenched and the methane-loss channel suppressed quantitatively by deuteration.
Related Concept Videos
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
¹H NMR of Labile Protons: Deuterium (²H) Substitution
Microbes and Methanogenesis
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Chemical Ionization (CI) Mass Spectrometry

