Medicinal plants constitute an important natural wealth of a country. They play a important role in providing primary health care services to rural people. They serve as therapeutic mediators as well as important raw materials for the manufacture of traditional and modern medicine. Substantial amount of foreign exchange can be earned by exporting medicinal plants to other countries. In this way indigenous medicinal plants play significant role of an economy of a country. Past century there has been
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flavor industries. The equilibrium of the reaction was changed by adding an excess amount of acetic acid. The reaction was refluxed and product was purified by extraction and distillation. Isopentyl acetate was analyzed by infrared spectroscopy and 1H NMR spectroscopy. Reaction Scheme: Mechanism: Key features of the Fischer Esterification mechanism are: a. protonation of the carbonyl group‚ b. the formation of the tetrahedral intermediate‚ and c. regeneration of acid to show its role of catalyst
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Introduction Chemists often find a method to determine the level of “greenness” of a chemical reaction‚ or its “atom economy”. A higher atom economy is preferable because a greater amount of the reactants will be present in the product as opposed to the byproduct.1 A Suzuki reaction is classified as an organic‚ coupling reaction that includes boronic acid and a halide that are catalyzed by a palladium complex under basic conditions. Other palladium- catalyzed coupling mechanisms include the Heck
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1.4 Formulation-related contaminations A few contaminations in a medication item or API can emerge from communications with excipients used to plan the medication item. During the time spent definition‚ a medication substance is subjected to different conditions that can prompt its debasement or different pernicious responses. For instance‚ if warmth is utilized for drying or for different reasons‚ it can encourage debasement of thermally labile medication substances. Arrangements and suspensions
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Borohydride Reduction of a Ketone Results 1. Draw a three-dimensional structure of the stereoisomer formed in the reaction. Name the compound. meso-Hydrobenzoin 2. Include other results as suggested by your data. * The attached IR and NMR spectroscopy data. * The melting point that ranges from 135.6-137.90C. Spectroscopic Analyses Data tables IR Spectroscopy Hydrobenzoin Peaks (cm-1) | Stretches | Intensity | 3332 (cm-1) | O—H stretch | Strong and broad | 3027 | C—H
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Experiment 4 Spectroscopic study of Cu(II) Complexes: Crystal Field Theory Objective: To study the effect of ligands on crystal field splitting energy ( E) Theory The color of coordination compounds of the transition elements is one of their characteristic properties. These colors are due to the absorption and subsequent emission of light in the visible part of the spectrum. Light in this region of the spectrum caused promotion of d–electrons from a lower to a higher energy level. The
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prepare 2-butanone from 2-butanol. Chromic acid was used in this experiment to in order to prepare 2-butanol. Cr (VI) is rather orange‚ but Cr (III) is dark green - therefore by oxidizing the alcohol (2-butanol)‚ an orange Cr (IV) is reduced to green. NMR and IR tests were taken to determine the result‚ and the crystallized derivative of this product was obtained. PROCEDURE: The experiment followed the instructions in the lab manual‚ except for the empty heating mantle‚ which our TA advised us to use
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indicative of a ketone. There are no bands that would be indicative of an NO2 group. This indicates that the nitrate group disappeared and was replaced with an amine group. NMR is a technique that measures both the molecular structure and the purity of the compound4. It does so by taking advantage of the polarity of the molecules4. NMR applies an external magnet to the molecule and‚ based on the change in energy of the protons‚ identifies if they are equivalent protons or not4. The larger the peak on
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where energy is proportional to frequency ( ) E~ f Electromagnetic Radiation • Electric field- responsible for most phenomena (transmission reflection‚ refraction and absorption) • Magnetic field responsible for absorption of RF waves in NMR Wave Properties of EM Radiation • Velocity‚ c = 3.0 × 108 m/s (vacuum) • Wavelength‚ λ characterizes type of radiation‚ units of length (e.g.‚ nm for Vis and UV‚ Aº for Xray) 1 • Wavenumber υ = ‚ cm-1 λ • Frequency‚ ν = c/λ‚ measured in s–1 (Hz)
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grade benzaldehyde together in a round bottom flask in propionic acid. This solution is then refluxed for about 30 minutes and the precipitate is dried by suction filtration. This product will be analyzed and classified by UV-Vis‚ FT-IR‚ and H1 FT-NMR. Once the product is determined to be TPP‚ it will be reacted with ZnCl2 and CuCl2 separately. An excess amount of the metal chloride will be added to a round bottom flask‚ along with the TPP‚ and will be refluxed for 30 minutes in the presence of DMF
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