dc.contributor.advisor | Guido Bugni | |
dc.contributor.author | Daly, Thomas | |
dc.date.accessioned | 2020-04-30T09:39:11Z | |
dc.date.available | 2020-04-30T09:39:11Z | |
dc.date.issued | 1967-04-01 | |
dc.identifier.uri | https://scholars.carroll.edu/handle/20.500.12647/186 | |
dc.description.abstract | Polyvinyl alcohol is a high molecular weight polymer whose repeating unit is CH2-CHOH. From this the expected monomer from which polyvinyl alcohol would be produced is vinyl alcohol, CH2=CHOH, however, vinyl alcohol does not exist in the free state, for it is very unstable in nature. Apparently, all reactions which would yield vinyl alcohol undergo a rearrangement to the more stable acetaldehyde or keto form. double bond in vinyl alcohol. This is caused by the desire to relieve the strain of the Rearrangements of this enol-keto type take place particularly easily because of the polarity of the 0-H bond and the very high electron density that attempts to become more stable by shifting a hydrogen. To relieve this strain, a hydrogen ion separates readily from oxygen, but when a hydrogen ion (most likely a different one) returns it may attach itself either to oxygen or to carbon. If it returns to oxygen, it may readily come off again; but if it attaches itself to carbon it tends to stay there. | |
dc.title | A Study Of The Synthesis Of Polyvinyl Alcohol | |
dc.type | thesis | |
carrollscholars.object.degree | Bachelor's | |
carrollscholars.object.department | Chemistry & Physics | |
carrollscholars.object.disciplines | Chemistry | |
carrollscholars.legacy.itemurl | https://scholars.carroll.edu/chemphys_theses/38 | |
carrollscholars.legacy.contextkey | 12930147 | |
carrollscholars.object.season | Spring | |
dc.date.embargo | 12/31/1899 0:00 | |