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The reaction of benzil with sodium borohydride (NaBH4) in the presence of water results in the reduction of the carbonyl groups to hydroxyl groups. This forms a mixture of diastereomers, hydrobenzoin, which is the major product, and iso-hydrobenzoin, which is the minor product. The reaction proceeds through a hydride transfer mechanism, where NaBH4 donates a hydride ion (H-) to the carbonyl group, leading to the formation of an alkoxide intermediate. This intermediate is then protonated by water to yield the final product.