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    Gringard Synthesis

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    Gringard Synthesis detailed procedure and scheme of the apparatus any changes to the original procedure‚ actual masses‚ and obs yield calculations and mp Discussion outline Grignard rxn (what is it used for‚ why important‚ the mechanism) Reaction set up (important details) How can the rxn be activated Second step: rxn of the Grignard reagent with acetophenone‚ quenching with ammonium chloride Isolation of the product‚ identification Possible or actual sources of error Part one of our experiment

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    Investigating How Concentration of Acid Affects the Reaction Between Calcium Carbonate and Hydrochloric Acid Introduction ============ According to the collision theory temperature‚ concentration‚ surface area and catalysts all affect rates of reaction as shown in the diagrams below. Increasing any of these should increase the number of collisions and so increase the reaction rate up to an optimum point. Increasing the temperature causes the particles to collide with more

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    Benzoic Acid

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    BENZOIC ACID & BENZOATES (210 –218) • Retards growth of bacteria and yeasts • Occurs naturally in many foods – a similar distribution to salicylate (but at a lower dose than as an additive) • Common food sources: Soft drink‚ cordial‚ fruit juice and cider Liquid essences and syrups Iceblocks‚ jelly‚ low joule jam‚ dips‚ pickles‚ olives Fish marinades and preserves • PABA (para-amino-benzoic-acid)

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    Determining Order from Rates of Reactions AP Chemistry Purpose The focus of this experiment is to recognize that when aqueous solutions of potassium iodate ion (KIO3-) and bisulfite ion (HSO3-) are mixed‚ a series of reactions will occur‚ and the final reaction is signaled by the appearance of a dark blue color. My partners and I investigate how the concentration of the reactants affects the rate of reaction. The purpose of this lab is to find

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    Alum Synthesis

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    Alum Synthesis: The Chemical Process of Recycling Aluminum Introduction By recycling aluminum cans‚ the costs and energy savings are dramatically more resourceful and efficient than producing aluminum from what it is naturally found in‚ bauxite ore. The process of recycling aluminum to produce potassium aluminum sulfate‚ a common alum‚ will be done through a serious of chemical reactions. Through this reaction‚ percent yield will be determined. Materials and Methods The mass of a 250 mL

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    Synthesis

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    Synthesis “The kingdom of heaven is within the mind of a person‚ not within the collective mindlessness of a crowd.” In the articles‚ “The Only True God and Jesus Christ Whom He Hath Sent”‚ by Jeffery R. Holland and “Propaganda under a dictatorship”‚ by Aldous Huxley are two totally different topics. This paper will be a breaking down of the two articles and finding the similarities between the two of them. It will be interesting‚ but nothing is impossible. The two topics are Hitler wanting so

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    Macrocyclic Synthesis

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    Lab Report Macrocyclic Synthesis (Heme Analog) I. Purpose of Experiment and Introduction The purpose of this lab experiment is to prepare meso-tetraphenylporphin (TPP) and its copper‚ cobalt or zinc complex by condensing benzaldehyde with pyrrole in boiling propanoic acid. II. Introduction and Background There are two types of proteins that function as oxygen carriers: myoglobin (stores the oxygen) and hemoglobin (present in red blood cells and is responsible for oxygen transport)

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    Synthesis of Acetanilide

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    Synthesis of Acetanilide By: Rick Whitely April 9‚ 2013 Organic Chemistry Lab 1; Professor J. Hutchison Recrystallization is a common method of purifying organic substances through the differences in solubility at different temperature. In this experiment‚ acetanilide was produced by acetylation of aniline with acetic anhydride. The crude acetanilide was dissolved in a solvent in a heated water bath. The solution was cooled slowly in an ice bath as crystals form out. As the compound crystallizes

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    ethers from alcohols H2SO4 R O R + H2O 2ROH  2. Williamson Ether Synthesis R O Na - - + + + R’X R O R’ + NaX     Ar O Na + RX Ar O R + NaX Involves a nucleophilic substitution reaction. Halide ion is displaced by the alkoxide or phenoxide ion. Gives best results when 1o alkyl halides are used. Mechanism is SN2.  Alkoxides may be prepared by reacting an alcohol with NaH or by reacting an alcohol with Na metal.  Phenoxides may be prepared by reaction of phenols

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    Abstract Introduction The acylation of the α carbon position of a carbonyl group is one of the greatest breakthroughs that has benefited chemists in organic synthesis particularly when in need of building a carbon skeleton of interest in a molecule. For one to be able perform this acylation technique‚ there are two mar approaches which are employable. The first method involves the deprotonation of the α-Carbon atom which has a pKa known to be ̴20 through the use of a strong base for instance

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