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One would expect that the reaction between an alkene and cold, dilute potassium dichromate is an oxidation to a bifunctional alcohol at the carbons in the double bond. The result is also called a vincinal diol or a glycol.

The reaction should be similar to the reaction of an alkene with cold, dilute potassium permangante, however, dichromate is a milder oxidizing agent and may not be as effective.

The mechanism for this reaction involves the formation of an intermediete 'ester' with the metal at the carbons of the double bond, breaking the double bond. The it can be shown that the resonance structure of the intermediete complex transfers electron density to the ester linkage and protonates from water at both of the ester sites completing the oxidation.

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Q: What happens when hexene reacts with cold neutral and dilute potassium dichromate?
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