-1Determination of an Unknown Liquid (2-butanol) Through Fundamental Analysis Lee Billips Department of Chemistry‚ Shippensburg University‚ 1871 Old Main Drive. Shippensburg‚ PA‚ 17257. Abstract: The identification and characterization of unknowns are an important part of organic chemistry. It is fundamental to know experimental methods to deductively identify compounds (1) . The determination of unknown #6 (2-butanol) was identified by a series of test; first taking the boiling point (94-96
Premium Chemistry Atom Temperature
EXPERIMENT NO. 6 LIPIDS I NUR 4 GROUP 9 POLICARPIO‚ JOHN PAUL (A & B) QUERUBIN‚ KIMBERLY (C & D) QUILALA‚ REGENE (E & F1) RAMOS‚ PRACCEDES (F2a & F2b) SABALDICCA‚ VENZ (F2c & F2d) INTRODUCTION Lipids are organic compounds found in living organisms that are insoluble or slightly soluble in water but soluble in non-polar organic solvents. Lipids can be classified into four groups which are -fats‚ oils‚ and waxes‚ -compound lipids‚ -steroids‚ and -derived lipids. Various
Premium Fatty acid Solvent Glycerol
six-membered ring structures. The process of a DielsAlder reaction involves a substituted alkene reacting with a conjugated diene in the cis conformation to create two new carbon-carbon σ bonds which results in the formation of a six-membered ring‚ as shown below: Figure 1: Example Diels-Alder reaction + 1‚3-butadiene ethene cyclohexene In the case of the reaction outlined in this report‚ the substituted alkene is maleic anhydride‚ and the conjugated diene is cyclopentadiene. The two undergo
Premium Chemistry Chemical reaction Organic chemistry
Chirality of Ethyl-3-hydroxybutanoate Generated from a Biological Pathway Jake Zimny LaSalle University Philadelphia‚ PA 19141 Submitted February 10‚ 2006 Abstract: The reaction being studied is a reduction of a ketone into an alcohol with a chiral center. Because a biological agent‚ bakers ’ yeast‚ is being used to drive this reaction‚ the optical purity that results in the product is so stereo-selective that the major product‚ (+)‚ is formed for 89% of the product. Introduction: This
Premium Alcohol Nuclear magnetic resonance
cyclo-alcohol to become a cyclo-ene. In this case 4-methylcyclohexanol was protonated using phosphoric acid to become 4-methylcyclohexene. This demonstrates the loss of an alcohol group by protonation‚ the loss of a proton from the cyclohexane to form an alkene through elimination. This also demonstrates Le Chatelier’s principle‚ by using distillation to remove the product as it is formed the equilibrium of the reaction will constantly be in favor of the product. Reaction: Side Reaction: Due to a
Premium Oxygen Alcohol Chemistry
Final Organic Study Guide: Be able to develop an Experiment Beginning to End * Find a good reaction * Good reaction is defined by high yield‚ green chemistry (less waste‚ less harmful chemicals) * Reaction found on Reaxys * Find MSDS Sheet for all Compounds (Reactants‚ Products and Side Products) * It is important to know what you are working with * The toxicity category numbers are there to gauge how toxic the chemical is‚ 4 being most severe and 1 being least
Premium Distillation Solubility Solvent
Cyclic dienes added to alkene dienophiles also lead to two new form of stereoisomeric products‚ the endo and exo products (Kilway‚ “Lecture”). In cases where dienes and dienophiles align above one another‚ the endo product is formed (Hunt). The endo product will have two axial substituent groups (Kilway‚ “Lecture”). This formation typically forms the major product because it takes less kinetic energy to be formed due to secondary orbital interactions with the substituents in transition states (Hunt)
Premium Alkene Oxygen Chemical reaction
PHYTOCHEMICALS AS NUTRACEUTICALS 08/08/2006 12:22 AM Phytochemicals as Nutraceuticals by Ben Best CONTENTS: LINKS TO SECTIONS BY TOPIC I. Introductory Remarks II . Terpenoids = Isoprenoids A . Carotenoid Terpenoids 1. Lycopene 2. Beta-Carotene 3. Alpha-Carotene 4. Lutein 5. Zeaxanthin 6. Astaxanthin B . Non-Carotenoid Terpeniods 1. Perillyl Alcohol 2. Saponins 3. Terpeneol 4. Terpene Limonoids III. Polyphenolics A . Flavonoid Polyphenolics 1. Anthocyanins 2. Catechins
Premium Cancer Antioxidant Atherosclerosis
SYLLABUS – ADVANCED PLACEMENT CHEMISTRY Required Texts 1. Chemistry: The Central Science by Brown‚ LeMay and Bursten‚ 10th ed.‚ Pearson Education. Inc.‚ Upper Saddle River‚ NJ‚ 2006‚ ISBN: 0131464892 Includes: Text book‚ Laboratory Manual‚ Student Study Guide‚ AP Test Prep Series‚ Solutions to Practice Problems 2. Barrons AP Chemistry‚ Jespersen‚ Neil D‚ 4th ed.‚ Barron’s Educational Series‚ Inc‚ 250 Wireless Boulevard‚ Hauppauge‚ New York 11788
Premium Chemistry Ion Chemical reaction
Groups/Pages: 1. PHDp: https://www.facebook.com/groups/PHD.Platform1/ 2. CRHPG (HUMLog): https://www.facebook.com/groups/CRPHC.HUMLOG/ 3. Pharma Tips: https://www.facebook.com/groups/pharmatips/ 4. BANGLORE/PUNE/HYDRBD JOB SEEKERS:https://www.facebook.com/groups/244121658956541/ 5. CDM & SAS: https://www.facebook.com/groups/clinicaldatamanagement/ 6. Indian Clinical Research & Health Care Professionals:https://www.facebook.com/groups/icrhcp/ 7. Pharma-Trend Setter: https://www.facebook.com/groups/pharmarockz/
Premium Infrared spectroscopy Nuclear magnetic resonance Spectroscopy