Quiz #1 Attempt 1 Written: Jul 7‚ 2012 9:48 AM - Jul 7‚ 2012 9:50 AM Submission View Your quiz has been submitted successfully. Question 1 1 / 1 point At what time do you have to complete your online prelab assignment to be allowed to participate in the lab? Question options: A week before the lab Day before the lab at 10 pm The morning of lab day at 8 am One hour before the lab Question 2 1 / 1 point Which materials/chemicals belong in the desiccator? Question options: Drying
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benzoin was obtained. The MP of benzoin was 127O-130O C and the IR spectra displayed a carbonyl peak at 3415 cm-1 ‚‚which represents and OH functional group. The second step of the reaction was to oxidize benzoin to form benzil; this reaction yielded 27.04% benzil. The MP of the benzil was 91O-93O C and the IR spectra revealed no OH functional groups. The last step of the synthesis was a double aldol condensation reaction to form tetraphenylcyclopentadienone; this reaction had a yield of 76.56% and
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Using Selective Media to Monitor the Fermentation Process of Cabbage and Cucumber‚ for Fourteen Days Abstract: Introduction: The goal of the ecological succession lab is to demonstrate succession with the fermentation of cabbage and cucumbers. The cabbage will ferment into sauerkraut and the cucumber will ferment to pickles during fermentation process that will changes the species structure and the community of time. During the fermentation process we watched the pH become more acidic‚ since
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Designation: D2972 – 08 Standard Test Methods for Arsenic in Water1 This standard is issued under the fixed designation D2972; the number immediately following the designation indicates the year of original adoption or‚ in the case of revision‚ the year of last revision. A number in parentheses indicates the year of last reapproval. A superscript epsilon (´) indicates an editorial change since the last revision or reapproval. 1. Scope 1.1 These test methods2 cover the photometric and atomic
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couple days. Determine the mass and mp of the recrystallized benzil and obtain an IR spectrum. Part C: Base-catalyzed aldol condensation of benzil and 1‚3-diphenylacetone (Week 4) Add 0.50 g of 1‚3-diphenylacetone‚ 0.50 g of benzil and 5 mL of triethylene glycol to a 50 mL round bottom flask. Add a stir bar and heat the mixture at setting 4-5 on heating manual for ~ 10-15 min (will not reflux boiling point too high). The benzil should dissolve during this time. Remove the heating mantle and
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was then in turn purified and used to synthesize Benzil in the next experiment through Copper (II) ion oxidation. The Benzil was obtained by catalytic oxidation of the Benzoin using the Copper (II) ion as the catalytic oxidant. The Benzil produced was then purified and used as the reactants in the third and final experiment of the sequence which was this one‚ to produce Tetraphenylcyclopentadienone which is a five-membered carboxylic ring. The Benzil was reacted with 1‚3- Diphenylacetone to undergo
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Jewellyn G. Diola; ladyjewellyndiola@yahoo.com Abstract Synthesis of 3‚4-dihydro-3-(p-methylphenyl)-1‚2-(2h)-benzoxazine involves the nucleophillic addition of the 1 °amine group upon the carbonyly group of the salicylaldehyde‚ the reduction of imine to amine and the addition of paraformaldehyde to proceed ring closure. The experiment prepared the product through Mannich reaction‚ a multicomponent condensation synthesis between ketone‚ aldehydes‚ enols and amines. Biosynthesis of benzoaxazines
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chromatography 3. Separation of a three – component mixture by extraction 4. Completion of experiments from day 1 to 4 5. NMR workshop 6. Sandmeyer Reaction: Preparation of p-chloronitrobenzene 7. Synthesis of benzilic acid from benzil 8. Aldol Condensation: Preparation of ethyl cinnamate 9. Isolation of caffeine from tea 10. Completion of isolation of caffeine from tea 11. Catchup day and completion of experiments School of Chemistry University
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Experiment II. Separation Of a Sample Mixture By Liquid-Liquid Extraction Reading assignment: Techniques in Organic Chemistry 2nd ed pages 75-99. 3rd ed pages 113-140. Topics and Techniques i) identification of solvent layers of two immiscible solvents ii) partioning of a compound between two immiscible solvents and determination of KD iii) liquid-liquid extraction with aqueous acids and bases with organic solvents. iv) use of drying agents Introduction Liquid-liquid extraction is a method
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Paracetamol - a curriculum resource Frank Ellis RSeC ROYAL SOCIETY OF CHEMISTRY Paracetamol - a curriculum resource Compiled by Frank E llis Edited by Colin Osborne and Maria Pack Designed by lmogen Bertin Published by the Royal Society of Chemistry Printed by the Royal Society of Chemistry Copyright 0 Royal Society of Chemistry 2002 Registered charity No. 207890 Apart from any fair dealing for the purposes of research or private study‚ or criticism or review‚ as permitted under
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