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    unknown mixture of colored compounds. The mixture will have three compounds from the following: azobenzene‚ azulene‚ 4-(p-nitrophenylazo)resorcinol‚ methyl red‚ bromocresol green. You can identify the components by separating them using thin layer chromatography (TLC) and comparing their Rf values with those of the

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    Drug Delivery System

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    contents; thin epidermal cells; lignified narrow spiral and annular vessels; scattered starch grains; rhomboid crystals of calcium oxalate; sclereids of the epidermis and dry scales. Identication (Thin Layer Chromatographic Identification Test for Crude Plant Drugs) – Test solution—Transfer 1.0g of dried allii sativi Bulbus Pulveratus to a suitable glass apparatus. Extract with 10mL of a mixture of methanol and water (95:5)‚ using any suitable method as described in Test Solution under Thin Layer Chromatographic

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    CRM PROJECT

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    opposition to‚ external forces like gravity Capillary action is sometimes called capillarity‚ capillary motion‚ or wicking Capillarity Types:- Capillarity Rise:- The upward movement of a liquid against the force of gravity inside narrow spaces and thin tubes is called capillary rise . This property of liquid is called capillarity. A common apparatus used to demonstrate capillarity is the capillary tube. Reason:- Capillarity occurs because of intermolecular forces between the liquid and surrounding

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    Medicine Analysis – Synthesising Aspirin results After recrystallisation differences between the crude and purified aspirin were noted. The impure (crude) aspirin was powered and fluffy with small clumps and was slightly yellow in colour whereas the pure aspirin has a less fluffy crystalline powder and was whiter. This showed distinct differences in the two substances but similarities were also apparent showing aspirin‚ in some level‚ was created. Before recrystallisation the crude aspirin could

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    between benzonitrile oxide and styrene. 2. Plan: Each student in a group of three will work to create a reaction with the Benzonitrile Oxide with‚ cis-stilbene‚ trans-stilbene‚ or styrene in an Erlenmyer flask. With this Reaction solution thin layer chromatography will be performed using each reaction solution. The different reactions will then be compared by running co-spot TLC’s. An NMR of the crude products from each reaction will be taken. 3. References: * Chemistry 173Q Organic Chemistry

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    Aspirin Preparation

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    melting point*Capillary tube *Tesco aspirin*Melting apparatus * synthesised aspirin | Apparatus for chromatography Materials for chromatography *Chromatography tank *Ethanol dichloromethane *Capillary tubes * Tesco pure aspirin *Weighing boat

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    Amino Acids

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    Separation of Amino Acids by Paper Chromatography Chromatography is a common technique for separating chemical substances. The prefix “chroma‚” which suggests “color‚” comes from the fact that some of the earliest applications of chromatography were to separate components of the green pigment‚ chlorophyll. You may have already used this method to separate the colored components in ink. In this experiment you will use chromatography to separate and identify amino acids‚ the building blocks of proteins

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    Chromatograph Lab

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    Chromatography Lab Questions Pre-Lab Questions 1. A pencil is used rather than a pen to mark the “starting line” in step two because a pen or marker while be used to place a small dot of ink in the center of the X that is made with a pencil. 2. Capillary action is filling of pores in a solid with a liquid. Capillary action is caused by spotting or absorption and is allowed to seep or flow through. 3. The type of pen that will probably give better separation in this paper chromatography

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    1. In table format‚ provide the Rf values you recorded for each of the 3 compounds in Part I. List compound on one axis of your table and solvent system on the other. If multiple spots were present for a compound‚ give Rf value for each component and state if the component was major or minor. | 100% hexane | 25% EtOAc in hexane | 10% EtOAc in hexane | Fluorene | 0.34 cm | 0.94 cm | 0.67 cm | 9 - fluorenol | 0.00 cm | 0.49 cm | 0.05 cm | 9 - fluorenone | 0.00 cm | 0.69 cm | 0.21 cm |

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    Chem Lab

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    physical properties. Paper chromatography will be used to separate the dye colors from M&M candy to see which colors contain yellow #5. Gravimetric separation will be used to separate salt and sand from a mixture. Procedure The procedure for this lab can be found on pages 16 – 30 in “General Chemistry CHE110L Laboratory Manual Fall 2013”. Data Tables Carbon copies of data tables have been attached to the back of this lap report. Calculations Paper Chromatography- 1. Yellow M&M’s Rf Value:

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