Apply the Felkin-Anh model to the stereocentre alpha to the ketone. Its large group is the chain continuing through the phenyl-bearing carbon, its medium group is methyl, and its small group is hydrogen. In the preferred transition-state arrangement, put the large group approximately perpendicular to C=O and approach from the opposite face, passing the small hydrogen along a Bürgi-Dunitz trajectory. The remote ether cannot form the usual small alpha-alkoxy chelate, and the coordinating solvent further supports using an open-addition prediction.[ref]
Felkin-Anh and Cram Chelate by University of Windsor. pp. 1–2: perpendicular large group and nucleophilic approach past the small group
The predicted new stereocentre is . In the question's zigzag projection, this corresponds to the new OH bond directed behind the page and the newly introduced methyl toward the reader, with the original stereocentres unchanged. The new-centre priority order is OH phenyl the substituted alpha-carbon chain methyl. This is a model-based major-product prediction, rather than a quantitative diastereomeric ratio.
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