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    3 Perylenepentanon

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    3-perylenepentanol‚ M4 39‚ 51 To a solution of 3-perylenepent-4-ynol‚ M3 (0.32 g‚ 0.957 mmol) in THF (20 mL)‚ Pd/C (600 mg‚ 3 wt% on activated carbon) was added. Nitrogen gas was turned off‚ hydrogen gas balloons were used to supply H2 gas to the flask. The reaction mixture was stirred for 15 h under hydrogen atmosphere at room temperature. Ethyl acetate was added to the reaction mixture and the Pd/C was removed by filtration. Solvent was removed in vacuo to afford 3-perylenepentanol as yellow solid

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    A simple‚ rapid‚ specific and highly sensitive spectrofluorimetric method has been developed for the quantification of dabigatran etexilate mesylate (DAB) in bulk and capsule dosage form. A linear relationship was found between fluorescence intensity and DAB concentration in the range of 0.01-1.0 μg/ml in DMSO as solvent at an emission wavelength of 391 nm after excitation at 334 nm‚ with a good correlation coefficient (0.989). The detection and quantification limits were found to be 0.005 and 0

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    accomplished by lining the developing chamber with filter paper. Place a trimmed sheet of filter paper in the jar. Perform the following 3 TLC experiments: Stationary phase Mobile phase TLC 1 Silica gel 95% ethanol TLC 2 Silica gel 1:1 water : acetic acid TLC 3 alumina 95% ethanol 4. Place the TLC strip into the developing chamber with the spotted end at the

    Free Chromatography Thin layer chromatography Ethanol

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    Yoyoma

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    The Preparation of Methyl Salicylate Introduction: Esters have various smells that differ due to the types of carboxylic acids and alcohols one mixes together. This is called esterfication. The reaction is catalyzed by an inorganic acid usually H2SO4 Purpose: In this lab Methanol alcohol and Salicylic acid were reacted together to form Methyl Salicylate. This was done to determine the characteristic odour of the Methyl Salicylate. Safety: Safety goggles must be worn at all times. Methanol: Toxic

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    behaviour? What is going on? “Drink driving is usually defined as driving with a specific amount of alcohol in the blood‚ known as an individual’s BAC – which can be measured from blood‚ urine‚ and breath tests that estimate the number of grams of ethanol per 100ml of blood.” (Reference: article 1) How is the behaviour performed? When? Where? Drink driving is performed when an individual drives a vehicle whilst over the legal BAC limit of 0.05 and 0.00 for Provisional drivers. It can be performed

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    3.1. Biochemical analysis of plant Due to the presence of bioactive compounds‚ medicinal plants have special properties of treatment of various chronic diseases. Lonicera quinquelocularis is used medicinally in the treatment of different diseases as “alternative medicine”. Due to the medicinal uses of the plant‚ it is very important to explore the biochemical composition of the plant. 3.1.1. Plant Collection Plant of Lonicera quinquelocularis was collected from the area Kakki of district Bannu‚ Khyber

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    different reagents; sodium iodide in acetone and silver nitrate in ethanol. Below the reaction equations 1. RX+NAIRI+NAX (X=Cl or Br) in the presence of acetone 2. RX+AgNO3+EtOHROEt+AgX+HNO3 We used three substrates primary secondary and tertiary compounds are 1-bromobutane‚ 2-bromobutane and 2-bromo-2-methylpropane respectively to react with the two nucleophiles that are sodium iodide with acetone solvent and silver nitrate with ethanol solvent. Based on lab analysis and the reaction mechanism we

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    genotoxicity of TE in terms of: mitotic index chromosomal aberrations micronuclei formation assess the developmental toxicity and teratogenicity potential of TE to zebrafish embryos; and verify the potential of TE to rescue zebrafish embryos from ethanol-induced teratogenicity. Place and Time of Study: The genotoxicity and teratogenicity/antiteratogenicity studies will be conducted in Caranglaan District‚ Dagupan City‚ and Don Mariano Marcos Memorial State University (DMMMSU) SLUC in Agoo‚ La Union

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    Photochemical Synthesis of Benzopinacol and its Acid-Catalyzed Rerrangement Product Benzopinacolone M.E.G. Balita Institute of Chemistry‚ University of Philippines‚ Diliman‚ Quezon City Date Performed: February 18‚ 2011 Date Submitted: March 4‚ 2011 Abstract In this experiment it is aimed to synthesize benzopinacol through photochemical reaction of benzophenone and‚ benzopinacolone via acid-catalyzed rearrangement of benzopinacol. In this experiment‚ mixture of benzophenone‚ isopropyl

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    Hbr To 1-Hexene

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    Discussion and Interpretation of Results The addition of HBr to 1-hexene created a 2-bromohexane‚ as indicated from the ethanol silver nitrate test and sodium iodide/acetone test. The observations when the product was subjected to these tests were similar to what were observed with the 2° bromide compound. When subjected to the silver nitrate test‚ the product produced a precipitate at the same rate of the 2° bromide compound‚ and the product produced a hue of yellow that was also similar to the

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