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Description
The use of thallium in carrying out difficult organic reactions and the role of 'synthetic methods' as an important area of research in chemistry.
Metadata describing this Open University video programme
Module code and title: S304, The nature of chemistry
Item code: S304; 25
First transmission date: 30-07-1977
Published: 1977
Rights Statement:
Restrictions on use:
Duration: 00:24:00
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Producer: David Jackson
Contributors: Alexander,1944 McKillop; Richard Taylor
Publisher: BBC Open University
Keyword(s): Organic; Synthesis; Thallium
Footage description: Footage - Periodic table (1'03"-1'10") - Blackboard with the position of thallium in the periodic table. Hypotheses for thallium (2'33"-6'30") - Diagram of the reaction of anisole with thallium triacetate & bromine leading to para bromoanisole. Demonstration of reaction (6'35"-8'34") - Diagram of mercuration reaction, thallium reaction & Friedel Crafts mechanism. Diagram of para bromoanisole (9'03"-10'19") - Diagram of an aromatic compound treated with thallium trifluoroacetate to form an arylthallium di trifluoroacetate (11'19"-11'40") - Diagram of metaxylene treated with thallium trifluoroacetate. Diagram of arylthallium di trifluoroacetate treated with potassium iodide to form the corresponding aromatic iodide & thallous iodide (12'05"-12'40") - Demonstration of thallation of metaxylene. Addition of aqueous potassium iodide to arylthallium di trifluoroacetate (12'51"-14'57"). Diagram of arythallium compounds (15'18"-17'05") - Diagram of oxythallation (18'29"-18'57") - Diagram of cyclohexene reacting with thallium trinitrate in methanol solution. Demonstration of oxythallation reaction. 2 4 di nitrophenol hydrozene added to cyclopentanecarboxaldehyde and methanol (19'09"-21'33") - Chemical equation of the direct oxidative rearrangement of acetephones to methyl aryl acetates (21'51"-22'17").
Master spool number: 6HT/72496
Production number: 00525_1233
Videofinder number: 908
Available to public: no