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Can you explain how the J values on HNMR support an E or Z configuration as...

Can you explain how the J values on HNMR support an E or Z configuration as it relates to the reaction of 2,3-dibromo-3-phenylpropanoic acid with acetone as the solvent, then with water as the solvent, to yield Beta-Bromostyrene. J values for Acetone give a ratio of 1:2 98%-cis 2%-trans. For Water it's 1:4 20%-cis, 80%-trans. Thank you.

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