Answer to Question 1The easiest way to determine if the reaction had gone to completion would be to wash a small sample of the Magtrieve mixture with a volatile solvent such as diethyl ether after 30 minutes and then analyze the mixture by TLC versus authentic samples of the starting material and product. If only the product is present, the oxidation is complete, but not all of the product has evaporated. If both starting material and product are present, then the reaction has not gone to completion, assuming an excess of Magtrieve was used.
Answer to Question 2The product would be the carboxylic acid, because such aqueous-acidic oxidations of primary alcohols lead to an over-oxidized product.
Answer to Question 3Although both are polar compounds, the alcohol can act as both a hydrogen bond donor and acceptor. The aldehyde can act only as a hydrogen bond acceptor. Therefore, the alcohol will have stronger interactions with the stationary phase resulting in a smaller Rf value relative to the aldehyde.