The goals of this experiment are to determine if the products derived from amide synthesis and Williamson Ether Synthesis are identical‚ and if one of the synthetic routes is more advantageous than the other. In Part 1‚ an attempt to synthesize acteophenetidin crystals by amide synthesis was made. We began by removing the colored impurities from the p-Phenetidine (reddish-brown) by placing 2g of the sample in 38 mL of hydrochloric acid and heating the solution to boiling point. Upon reaching just
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Purpose Acetophenetidin can be formed through two methods‚ Williamson ether synthesis and amide synthesis. By working in groups of two we were able to complete both methods of synthesis routes. The end result should be the synthesis of a similar product‚ by verification between the two individuals. Reaction Experiment and Observations Amide Synthesis of Acetophenetidin The Synthesis reaction began by removing the colored impurities from the p-phenetidine‚ accomplished by mixing
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The Basics of NMR Chapter 1 INTRODUCTION [pic] NMR Spectroscopy Units Review [pic] NMR Nuclear magnetic resonance‚ or NMR as it is abbreviated by scientists‚ is a phenomenon which occurs when the nuclei of certain atoms are immersed in a static magnetic field and exposed to a second oscillating magnetic field. Some nuclei experience this phenomenon‚ and others do not‚ dependent upon whether they possess a property called spin. You will learn about spin
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Binding curves: CD can be used to monitor the binding if s substrate to a protein. The substrate can give a very different CD spectrum when free in the solution relative to when bond in solution. Outside of farUV: 180-240nm. 1. Near UV CD: 240n-320nm‚ Aromatic amino acids and disulphide bonds. 2. Visible CD: d-d transition in some metal protein complexes for eg Cu (II) prion. Principles of Chromatography
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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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Preparation of a mixture of methyl‚ ethyl and 2-propyl salicylates and determination of % ratio by GC and HNMR spectroscopy INTRODUCTION: Figure 1: Formation of ester from carboxylic acid. MECHANISM: When the carboxylic acid is treated along with the acid catalyst and alcohol[R-OH]‚ It gives rise to the formation of ester along with water. Furthermore alcohol is used in an excess amount
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Bull NMR Post Lab Report Abstract Viewed as one of the most significant tools in analytical chemistry‚ the Nuclear Magnetic Resonance (NMR) is a spectroscopy tool often used by chemists to determine the molecular profile – quality and quantity of the major components - of any given organic substance. Operating on basis of spectroscopy (study of the interaction between matter and radiated energy - Harris)‚ the NMR can be either a one (1H NMR) or two (1H/13C NMR) dimensional spectral analysis that
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8. Terfenedine is an amino diol that is the active ingredient in the antihistamine Seldane. Mass spectral analysis of terfenedine shows a molecular ion at m/z = 471 and a peak at m/z = 472 which is 35.5% the height of the molecular ion. Terfenedine is known to contain C‚ H‚ O and N. (a) Suggest five molecular formulas for terfenedine. (b) Terfenedine has an even number of carbons and contains nine double bonds and four rings. Based on this additional information‚ what is the formula for terfenedine
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Abstract – This multi-step synthesis uses aniline as the starting reagent to synthesize five compounds employing several reactions such as acetylation‚ diazo coupling‚ nitration‚ bromination‚ and hydrolysis. The isolated products were analyzed with TLC and spectral data that determined most products were pure while some had a few impurities indicated by GC‚ LC‚ and a wide melting point range was shown for products 2 and 3. The presence of water in product 2 and 7 was indicated by the IR. Acetanilide
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Discussion & Error Analysis: By examining the unknown alcohol’s H NMR spectra‚ it can be deduced that the alcohol is 1-(3-methoxyphenyl)ethanol. There are three peaks that have a shift of ~7.0-7.5‚ one with integration values of 1‚ 2‚ and 1.This shows that the alcohol is a meta-substituted benzene ring. The singlet peak with a chemical shift of~ 4.7 ppm with an integration of 1 is from the hydrogen on the OH group. The peak at ~ 1.7 ppm corresponds to the hydrogen of the carbon that is attached
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