NMR Project Sample 35 and 40 Chemical Engineering Chemical Analysis Aim The two samples are 35 and 40. Analytical techniques are vital in everyday science and so NMR procedure is an absolute essential to deduce compounds and chemical structures; this assignment requires the identification of two samples using an NMR software program. Background NMR spectroscopy is a well established method for structure determination of various organic molecules ranging from small molecules all the
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The 13C NMR spectrum was useful to help finding the structure of the unknown. It showed six different signals in the spectrum. Signal 1 had an observed peak value of 19.242 ppm‚ and its peak calculated value was 19.1 ppm. This signal was first to most upfield and shielded in the spectrum because of the high electron density of carbon. This signal was agreed to a literature value for a CH3 group between 5-30 ppm. Signal 2 was branched to signal 1‚ and had the same value‚ but it was agreed for the
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Epoxidation Reactions Lab Report 2 Abstract An oxygen atom is transferred from a peroxy acid to the carbon=carbon double bond thus forming an epoxide. Scheme 1. Oxone Epoxidation. Scheme 2. mCPBA Epoxidation. The percent yield for the Oxone epoxidation reaction was 65% yield and the mCPBA epoxidation reaction was 70% yield. Oxone is the greener alternative because using mCPBA is twice as expensive as Oxone and leaves behind the epoxide plus m-chlorobenzoic acid while Oxone creates non-toxic
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General Papers ARKIVOC 2006 (i) 109-118 Synthesis and primary antiviral activity evaluation of 3-hydrazono-5-nitro-2-indolinone derivatives Nalan Terzioğlu *a‚ Nilgün Karalı a‚ Aysel Gürsoy a‚ Christophe Pannecouque b‚ Pieter Leysen b‚ Jan Paeshuyse b‚ Johan Neyts b‚ and Erik De Clercq b a Istanbul University‚ Faculty of Pharmacy‚ Department of Pharmaceutical Chemistry‚ 34116‚ Istanbul‚ Turkey b Rega Institue of Medical Research‚ Katholieke Universiteit Leuven‚ B-3000 Leuven‚ Belgium E-mail:
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Abstract Chemically active extraction was used to separate two unknown compounds from each other and to determine what compound class each compound belongs. The solid unknown was purified by recrystallization and its melting point range was determined to be 109-111°C. The liquid unknown was purified by simple distillation and its boiling point was determined to be 95°C. An IR spectrum was collected for each of the purified compounds; the solid was determined to be 3-toluic acid and the liquid was
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Experiment 1: Preparation of 1-Bromobutane and Reactivity of Alkyl Halides Objective: The purpose of this lab is to prepare 1-bromobutane from 1-butanol in an acid-catalyzed substitution reaction. While the reaction would be expected to occur as SN2 due to the primary nature of the substrate‚ because H2SO4 is used as a solvent‚ the conditions are very polar and the reaction can proceed via an SN1 reaction. The main objective is to obtain test results to determine the mechanism of the reaction
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Organic Chemistry II Laboratory (ABCT357) Although studying fundamental theories of chemistry in the class is important to understand the concept of chemistry‚ carrying out experiments to corroborate the theories is also important. It is very important for students to get used to experiments in order to speed up their experiments. Expt.1. Acetylation of α-D-glucopyranose Add slowly 2.5 g (0.014 mol) of powdered D-glucose in small portions (roughly in 7-10 portions and 5 min for each addition)
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Thiamine-Catalyzed Benzoin Condensation I.Conclusion Benzoin was produced by reacting 2 mols of benzaldehyde with the catalyst thiamine to form a new C-C bond. A total of 2.626 grams were recovered. There was a 33% recovery of benzoin. The low percent recovery could be due to the purity of the limiting reactant‚ benzaldehyde. Upon filtration‚ the mother liquid appeared oily making it more likely that the low recovery was due to the solution ‘oiling out.’ This could be avoided in the future
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L09 Tree Balancing CX1007 Data Structures 2013/14 S2 Mark Yong Today • Importance of balance for BSTs • Balancing operaGons in self-‐balancing BSTs • Pseudocode + worked examples CX1007 Data Structures 2013/14 S2 2 Recall: Why use BSTs? • BSTs are a special form of BT L • At every
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Organic Chemistry II Laboratory (ABCT357/ABCT3757) Lab Manual 2014-2015 Lee Hang Wai‚ Alston (alston.lee@polyu.edu.hk) Dr. Lee Cheng Hao‚ Samuel (chenghao.lee@polyu.edu.hk) Organic Chemistry II Laboratory (ABCT357‚ ABCT3757) (Group one) Contact: Alston Lee (alston.lee@polyu.edu.hk) Tuesday 8:30-11:30 ‚ Laboratory: Y1315 Lab supporting staffs: YK Au / Kan Chan/Arnold Demonstrators: Dr. Samuel Lee‚ Alston Lee‚ Fu Wai Chung‚ Guo Shuai‚ Yuen On Ying‚ Sep 16 Tue Acetylation of α-D-glucopyranose (Expt
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