{"id":{"repo_id":"wku-diss","oai_identifier":"oai:digitalcommons.wku.edu:theses-2014"},"canonical_url":"https://search.dev.ndltd.org/etd/wku-diss/oai:digitalcommons.wku.edu:theses-2014","repository":{"repo_id":"wku-diss","name":"Western Kentucky University","base_url":"https://digitalcommons.wku.edu/do/oai/"},"display":{"title":"The Reduction of Carbonyl Compounds by Sodium Naphthalenide","abstract":"The purpose of this investigation was to study the reactions of sodium naphthaienide with various aromatic carbonyl compounds, particularly aromatic aldehydes and ketones. Although sodium naphthalenide was first investigated in 1936 by Scott et al, the synthetic utility of this alkali metal adduct in organic chemistry has only recently been explored. It was thought that sodium naphthalenide might provide a synthetic advantage, as compared to sodium metal solutions, in the reduction of carbonyl functions to their respective glycols and/or alcohols.","abstract_html":"The purpose of this investigation was to study the reactions of sodium naphthaienide with various aromatic carbonyl compounds, particularly aromatic aldehydes and ketones. Although sodium naphthalenide was first investigated in 1936 by Scott et al, the synthetic utility of this alkali metal adduct in organic chemistry has only recently been explored. It was thought that sodium naphthalenide might provide a synthetic advantage, as compared to sodium metal solutions, in the reduction of carbonyl functions to their respective glycols and/or alcohols.","abstract_has_math":false,"creators":["Stinnett, James"],"institution":null,"degree_name":"Master of Science","degree_level":null,"degree_discipline":"Department of Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1971,"date_issued":"1971-11-01T08:00:00Z","date_published":"1971-11-01T08:00:00Z","updated_at":"2026-07-24T06:08:02Z","subjects":["Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.wku.edu/theses/1011","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Stinnett, James"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Department of Chemistry"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Chemistry"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.wku.edu/theses/1011"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The purpose of this investigation was to study the reactions of sodium naphthaienide with various aromatic carbonyl compounds, particularly aromatic aldehydes and ketones. Although sodium naphthalenide was first investigated in 1936 by Scott et al, the synthetic utility of this alkali metal adduct in organic chemistry has only recently been explored. It was thought that sodium naphthalenide might provide a synthetic advantage, as compared to sodium metal solutions, in the reduction of carbonyl functions to their respective glycols and/or alcohols."]},{"key":"dc:title","label":"Title","values":["The Reduction of Carbonyl Compounds by Sodium Naphthalenide"]}]}],"canonical_facts":{"dc:creator":["Stinnett, James"],"dc:description.abstract":["The purpose of this investigation was to study the reactions of sodium naphthaienide with various aromatic carbonyl compounds, particularly aromatic aldehydes and ketones. Although sodium naphthalenide was first investigated in 1936 by Scott et al, the synthetic utility of this alkali metal adduct in organic chemistry has only recently been explored. It was thought that sodium naphthalenide might provide a synthetic advantage, as compared to sodium metal solutions, in the reduction of carbonyl functions to their respective glycols and/or alcohols."],"dc:identifier":["https://digitalcommons.wku.edu/theses/1011"],"dc:subject":["Chemistry"],"dc:title":["The Reduction of Carbonyl Compounds by Sodium Naphthalenide"],"dc:type":["Thesis"],"thesis:degree_discipline":["Department of Chemistry"],"thesis:degree_name":["Master of Science"]},"updated_at":"2026-07-24T06:08:02Z"}