Acetaminophen KBr pellet provided a handful of strong peaks and hints that helped us to hypothesize what functional groups might be in Acetaminophen. The peaks that were at the highest wavenumbers were analyzed first. The strong peak at 3325.82 cm-1 was an indicator that there was stretching occurring between a Hydrogen and Nitrogen atom. This signified that Acetaminophen could contain an amide group. The next defined peak is located at 3162.26 cm-1‚ and the section between these two peaks has a slight
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UNIVERSITY TUNKU ABDUL RAHMAN FACULTY OF SCIENCE BACHELOR OF SCIENCE(HONS)BIOCHEMISTRY YEAR 1 SEMESTER 1 UDEC1164 ORGANIC CHEMISTRY Name: Cheong Wai See Student ID: 1404057 Practical Group: 1 Title of Experiment: Name of Tutor: Dr. Mohammod Aminuzzaman Date: 24 February 2016 Tiltle: Nitration of Methyl Benzoate Objectives: -To prepare methyl-3-nitrobenzoate from nitration of methyl benzoate by electropilic aromatic substitution. -To calculate the percentage yield and get the melting point of methyl-3-nitrobenzoate
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Richard F. Daley and Sally J. Daley www.ochem4free.com Organic Chemistry Chapter 2 Introduction to Organic Nomenclature and Functional Groups 2.1 Drawing Organic Structures 73 2.2 Alkanes 77 2.3 Structural Isomerism 77 2.4 IUPAC Nomenclature 79 2.5 Naming Alkanes 80 2.6 Naming Cycloalkanes 87 2.7 Naming Complex Alkyl Groups 2.8 Functional Groups 97 2.9 Naming Alkenes and Alkynes 2.10 Naming Alkenes‚ Part II 108 2.11 Arenes 109 2.12 Organohalogens 113 2.13 Using Molecular
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Anhydride Product IR Data: Functional Group or Bond Peak Location(s) (cm-1) Peak Intensity Symmetric C=O Stretch 1840 Weak Asymmetric C=O Stretch 1765 Strong C-O Stretch 901 Very strong Table 3: Dicarboxylic Acid Product IR Data: Functional Group or Bond Peak Location(s) (cm-1) Peak Intensity C=O Stretch 1702 Strong O-H Stretch 3200-2500 Broad‚ medium Sp2 C-H Stretch(s) 3021‚ 3082 Medium Table 4: Lactone (Unknown) Product IR Data Functional Group or Bond Peak Location(s)
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1. The following compound A‚ is used as an artificial sweetener. Compound A (April 2009) (a) Name all functional groups in A (b) For each of the carbon X‚ Y and Z in compound A‚ determine (i) the type of hybridization (ii) the bond angle (c) A is optically active. Mark on the structure the chiral centre(s) in A. 2. (a) Draw structural formula of (i) a haloalkane
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SUBJECT: Organization Behavior Case-1- A WINDOW ON LIFE For Gilbert La Crosse‚ there is nothing quite as beautiful as a handcrafted wood-framed window. La Crosse’s passion for windows goes back to his youth in Eau Claire‚ Wisconsin‚ where he learned from an elderly carpenter how to make residential windows. He learned about the characteristics of good wood‚ the best tools to use‚ and how to choose the best glass from local suppliers. La Crosse apprenticed with the carpenter in his small workshop
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Research Article Vol: 2; Issue: 1 SYNTHESIS AND ANALYSIS OF BENZOPINACOL FROM BENZOPHENONE BY PHOTOREDUCTION IN GREEN CHEMISTRY. 1 Lata.C.Potey‚ 2* Dr. Satish B. Kosalge‚ 3 Rajeshwari S. Sarode 1 2 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Principal‚ Hi-Tech College of Pharmacy‚ Chandrapur 3 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Date Received: 11 TH Jan 2014 Date of Accepted: th 16 Jan 2014 Date Published: 18th
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everyday life‚ and to become familiar with the principles of bonding‚ nomenclature of various organic groups‚ terminology‚ structure/properties (physical and chemical) relationship‚ molecular geometries as well as simple reaction mechanism. Detailed objectives are as follows. 1. The student will be able to distinguish between organic and inorganic compounds and recognize important organic functional groups. 2. The student will be able to draw Kekulé‚ condensed‚ and skeletal structures for organic compounds;
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(–C(O)–OH) as a functional group are called carboxylic acids. The –C (O)-OH group which itself is made up of a carbonyl group (>C=O) and a hydroxyl group (-OH) is called a carboxyl group (carb from carbonyl and oxyl from hydroxyl group). Carboxylic acid may be an aliphatic or an aromatic depending upon whether –C–OH is attached to an alkyl group ( or a hydrogen atom) or an aryl group. Their general formulas are; ALIPHATIC CARBOXYLIC ACID: R–C (O)–OH where R=H or an alkyl group. Example: AROMATIC
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Amines and Amides Amine - an ammonia molecule (NH3) in which one or more H atoms are substituted by an alkyl or aromatic group. Amide - an organic compound with a carbonyl functional group (C=O) bonded to a nitrogen atom. Amines are the smaller and simpler products of the decomposition of larger and more complex organic compounds like proteins. They often have foul odours‚ as do many nitrogen compounds‚ such as the smell of rotting fish and decomposing animal tissue and are produced by
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