"Carbonyl" Essays and Research Papers

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    Experiment # 45: Benzocaine Abstract The local anesthetic‚ benzocaine‚ was synthesized via the esterification of p-aminobenzoic acid with ethanol. The percent yield of crude product was determined to be 21% and the melting point was recorded at 86.2°C ± 0.2°C‚ with a 6.3% error from 92°C‚ the literature melting point of pure benzocaine. The crude product was then recrystallized to improve the purity of benzocaine and 57.4% was recovered. The new melting point range was measured at 89.1°C ±

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    Radiations of GSM Base Station Antenna And Its Health Consequences- A Research conducted in Nigeria In Nigeria 98% of Global System for Mobile (GSM) base stations (cell sites) are sited within 20 meters from residential‚ offices‚ schools‚ business buildings. Cell phone antennas emit microwave frequencies‚ which are non-ionizing radiation. A research was conducted by measuring field data of radiation from GSM base antennas in Nigeria for supporting evidence public health risks from gsm radiations

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    Our data displayed supports the notion that by increasing the acidity of the catalyst‚ the production of aspirin will increase. Our hypothesis was proven correct. In our data‚ we calculated the percent yield and percent error of each trial. We also calculated the average of the percent yields and the percent errors of each catalyst. In the end‚ we saw that for the sulphuric acid catalyzed aspirin‚ we saw an average of 69.7% percent yield and an average 30.3% percent error. As for the phosphoric acid

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    Organic chemistry

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    Chapter 17—Alcohols and Phenols SHORT ANSWER Drawing Instructions: Draw structures corresponding to each of the given names. 1. Draw: cis-4-tert-butylcyclohexanol ANS: 2. Draw: 3-methyl-2-buten-1-ol ANS: 3. Draw: 2-phenyl-2-propanol ANS: 4. Draw: glycerol ANS: 5. Draw: 2‚ 4‚ 6-trinitrophenol ANS: IUPAC Naming Instructions: Provide proper IUPAC names. 6. Name: ANS: (E)-2-ethylbut-2-en-1-ol 7. Name: HOCH2CH2OH ANS:

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    Orgo 1 Study Guide

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    Introduction to Alkane Nomenclature A. Determining the Priority of Functional Groups. What’s in a name? 3-ethyl-5-(1-methylpropyl)-4‚4-dimethylnonane Too big a subject to cover on one sheet! This paper will focus on alkanes. Determining functional group priority will be the subject of a subsequent sheet. suffix http://masterorganicchemistry.com D. Applying the Lowest Locator Rule F. Dealing With Branched Substituents (the IUPAC Way) Number the chain from one end so as

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    Preparation of 4-bromoaniline Introduction Aromatic compounds tend to undergo electrophilic aromatic substitutions rather than addition reactions. Substitution of a new group for a hydrogen atom takes place via a resonance-stabilized carbocation. As the benzene ring is quite electron-rich‚ it almost always behaves as a nucleophile in a reaction which means the substitution on benzene occurs by the addition of an electrophile. Substituted benzenes tend to react at predictable positions. Alkyl groups

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    placement of atoms; they are enatomers of each other. Organic chemistry create plentiful necessities like medications and other inventions. For instant‚The breath analyzer that detects drunk drivers uses the reaction of alcohol with chromium to form carbonyl

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    adol condensation and therefore produce Tetraphenylcyclopentadienone. The first step of the reaction to from the Tetraphenylcyclopentadienone requires the loss of -hydrogen to the base‚ resulting in a negatively charged carbon that bonds with the carbonyl group from the benzil. The bonding then

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    SCH4U Exam Study Notes

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    Compiled SCH4U Course Review Unit 1: Atomic Structure and Bonding Section 3.3 Electron Configurations and Periodic Trends (pg. 139-157) Feb. 11 For single electron system all orbitals with the same value of have the same energy Atoms with more than 1 electron with the same value of n have different energies (sublevels) Because of interactions between additional electrons All orbitals within a sublevel have the same energy The Fourth Quantum Number: A property of the electron (spin quantum

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    grignard synthesis

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    Lab 3: Grignard Synthesis Objective: The goal of this lab is to synthesize a Grignard reagent from bromobenzene and magnesium metal in diethyl ether. This same Grignard reagent would then be used to prepare a tertiary alcohol and then purify and characterize the product. Table of Reagents: Name Chemical formula Melting Point Boiling Point Density Safety Hazards Diethyl ether C4H10O -116.3°C 34.6°C 0.7134 g/ml Flammable Bromobenzene C6H5Br -30.6°C 156°C 1.5 g/ml

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