Chemistry Laboratory Report (Magnesium Oxide) INTRODUCTION: As we learned before on how to determine the empirical formula of a compound based on the test and also chemical analysis on it. Hence this experiment is mainly goes around with how to determine the empirical formula of Magnesium Oxide following various tight procedures in order to get the knowledge and apply it onto another compounds. We are investigating the empirical formula of Magnesium Oxide in this experiment. RESEARCH QUESTION:
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test the law of definite proportions for the synthesis reaction of combusting magnesium. In this lab‚ the polished magnesium ribbon was placed in covered crucible and was heated in order for it to react with Oxygen presented in air and in water provided. The result showed that Magnesium oxide formed through chemical reaction was made up of 60.19% magnesium and 39.81% oxygen‚ which is approximate proportion of both particles in every Magnesium oxide compound. From this lab it can be concluded that the
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Exercise No. 8 CARBOXYLIC ACIDS AND ACID DERIVATIVES I. OBJECTIVES: • To investigate the physical and chemical properties of Carboxylic acid and its derivatives • To understand the reactions of carboxylic compounds and derivatives. II. EXPERIMENTAL RESULTS Solubility of Carboxylic acids in 10% NaHCO¬3 Acetic acid - formation of bubbles Benzoic acid - formation of bubbles Test for Acetic acid NaOH + Acetic acid - blue litmus paper turned red NaOH + Acetic acid + FeCl3 - red colored
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Stereochemistry of Butenedioic Acid Objective: To study the interconversion of two geometric isomers‚ maleic acid (cis isomer) to fumaric acid (trans isomers)‚ the differences in physical properties between this pair of cis-trans isomers and determine the stereochemistry of addition of bromine to butenedioic acid. Chemicals and Apparatus: 2 grams of maleic acid‚ 10 cm3 of concentrated hydrochloric acid‚ 10 cm3 of bromine water[1]‚ one 50 cm3 beaker‚ one 100 cm3 beaker‚ one 250 cm3
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CARBOXYLIC ACID Introduction: Organic compounds containing (–C(O)–OH) as a functional group are called carboxylic acids. The –C (O)-OH group which itself is made up of a carbonyl group (>C=O) and a hydroxyl group (-OH) is called a carboxyl group (carb from carbonyl and oxyl from hydroxyl group). Carboxylic acid may be an aliphatic or an aromatic depending upon whether –C–OH is attached to an alkyl group ( or a hydrogen atom) or an aryl group. Their general formulas are; ALIPHATIC CARBOXYLIC ACID: R–C
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Chemistry Practical Report: Topic: Determining the Empirical Formula of Magnesium Oxide Patrick Doan 11 CHEM 11 26/9/08 Table of contents 1.0 Aim 1 2.0 Theory 2-3 3.0 Materials 4 4.0 Method 4 5.0 Results 4 - 5.1 Qualitative Observations 4 - 5.2 Example Calculations for each Calculated Value 5-7 -5.21 Experimental Values and Associated Errors 5-7 - 5.3 Accumulated Raw Data 8 - 5.4 Mean Experimental
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Acid Property #1: The word acid comes from the Latin word acere‚ which means "sour." All acids taste sour. Well known from ancient times were vinegar‚ sour milk and lemon juice. Aspirin (scientific name: acetylsalicylic acid) tastes sour if you don’t swallow it fast enough. Other languages derive their word for acid from the meaning of sour. So‚ in France‚ we have acide. In Germany‚ we have säure from saure and in Russia‚ kislota from kisly. Base Property #1: The word "base" has a more complex
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Kinetics Kinetics 6.1 Rates of reaction 6.2 Collision theory 6 16.1 Rate Expression (AHL) 16.2 Reaction mechanism (AHL) 16.3 Activation energy (AHL) 6.1 Rates of reaction 6.1.1 Define the term rate of reaction. 6.1.2 Describe suitable experimental procedures for measuring rates of reactions. 6.1.3 Analyse data from rate experiments. © IBO 2007 Figure 601 An explosion is a quick reaction D ifferent chemical reactions occur at different rates (i.e. speeds)
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Amino Acids Glycine is the smallest of the amino acids. It is ambivalent‚ meaning that it can be inside or outside of the protein molecule. In aqueous solution at or near neutral pH‚ glycine will exist predominantly as the zwitterion. Alanine is a hydrophobic molecule. It is ambivalent‚ meaning that it can be inside or outside of the protein molecule. The α carbon of alanine is optically active; in proteins‚ only the L-isomer is found. Serine differs from alanine in that one of the methylenic
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Preparation and properties of boric acid Result The mass of borax‚ g | 10.0734 | The mass of watch glass‚ g | 36.2842 | The mass of watch glass with product‚ g | 39.9803 | The mass of product‚ borix acid‚ g | 3.6961 | Test | Result | Boric acid is dissolved in water and methyl red indicator is added. | Pink solution is observed | Mannitol is dissolved in water and methyl red indicator is added. | Pink solution is observed | Both solution is added together | The colour of solution
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