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Isotopic branching in methane oxidation: fate of deuterium in CH3D + OH

Ascertain whether, in the grain-surface reaction involving deuterated methane (CH3D) and OH within H2O-rich ices, the deuterium atom preferentially transfers to the methyl radical (forming CH2D) or to water (forming HDO), and determine whether this methane-oxidation pathway can subsequently produce deuterated methanol via CH3 + OH → CH3OH under prestellar core conditions.

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Background

Methanol can form in H2O-rich ices before CO freeze-out via CH4 + OH → CH3 + H2O followed by CH3 + OH → CH3OH. If CH3D or OD is present, deuteration could occur along this route.

The isotopic fate of D in the initial CH4 + OH step (to CH2D vs. HDO) critically determines whether this pathway contributes to deuterated methanol formation.

References

However, it is not known, if the D atom in CH$_3$D prefers to go into CH$_2$D or into HDO in Eq. \ref{eq:Qasim1}; and thus, if it even has the potential to form deuterated methanol.

First Detection of CH3OD in Prestellar Cores (2511.03581 - Kulterer et al., 5 Nov 2025) in Section 5.1 (Origins of Prestellar Methanol Deuterium Fractionation Patterns)