Epoxide reacting with Tosylic Acid and Water

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Epoxide rings can be opened by water in an acidic environment, leading to the formation of diols. The expected product from the reaction with tosyl acid and water is 1-methyl-1,2-cyclohexanediol. The discussion focuses on determining the stereochemistry of this product. Participants are encouraged to provide insights on the stereochemical outcomes of the reaction. Clarification on stereochemistry is sought to complete the understanding of the reaction's product.
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Homework Statement


I was given the reaction in the attachment, and asked to find the product.

2. The attempt at a solution
My understanding is that water can open epoxide rings, in an acidic environment. And so, I would figure that the product is 1-methyl-1,2-cyclohexanediol. I don't know what the stereochemistry would be.

Any help?
Thanks,
Peter
 

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Any suggestions for the stereochemistry of this reaction?
 

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