Limiting Reagents and Percentage Yield Worksheet 1. Consider the reaction I2O5(g) + 5 CO(g) -------> 5 CO2(g) + I2(g) a) 80.0 grams of iodine(V) oxide‚ I2O5‚ reacts with 28.0 grams of carbon monoxide‚ CO. Determine the mass of iodine I2‚ which could be produced? 80 g I2O5 1 mol I2O5 1 mol I2 1 333.8 g I2O5 1 mol I2O5 28 g CO 1 mol CO 1 mol I2 253.8 g I2 1 28 g CO 5 mol CO 1 mol I2 b) If‚ in the above situation‚ only 0.160 moles‚ of iodine‚ I2 was produced
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FOUNDATION IN SCIENCE INTRODUCTION TO PRACTICAL ORGANIC CHEMISTRY – MAKING AND PURIFYING ORGANIC COMPOUNDS Stage 1 – Deciding how much reagent to use Most organic reactions do not go to completion; most reach an equilibrium position with significant quantities of reactants still remaining. In addition‚ separating the desired product from the rest of the reaction mixture‚ and then purifying it‚ will result in the loss of more of the product. The amount of product obtained expressed as a percentage
Free Distillation Sulfuric acid Acetic acid
out an order that if there is any influences and which of these temperatures make the biggest influence. Objects Experiment A: There will be six test tubes are set up‚ which contains one control variable and five different types of substrates: Cyclohexanol‚ (1‚ 4) - Cyclohexandiol‚ (1‚ 2) - Cyclohexanediol‚ Catechol‚ Resourcinol. The darkness of these five test tubes will be the depended variables. Experiment B: There will be eleven test tubes are set up‚ which contains one control variable and
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Alkane‚ Alkene‚ Alkyne & Aromatic Learning Objectives 1. 2. 3. Determine the IUPAC name‚ common name and structure of an alkanes‚ alkenes and cycloalkanes. Identify the physical properties of alkanes. Describe briefly natural sources and importance of alkanes Describe reactions of alkanes Propose a mechanism on free radicals substitution 4. 5. 6. Describe the preparation and reactions of alkenes. 7. Propose mechanism on preparation; dehydration of alcohol 8. Define carbocation
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Paul Hermann Diels and Kurt Alder first documented this type of reaction‚ hence the name Diels-Alder reactions. Their reaction is one of the more useful reactions done in chemistry because it does not require very much energy in order to make the cyclohexene ring and the result can create four stereo centers‚ making it compatible for a variety of functional groups which still has double bonds in the products. Dimethyl Tetraphenylphthalate. Tetraphenylcyclopentadienone (0.100g)‚ dimethyl acetylene-dicarboxylate
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H.B Fuller and the Street Children Of Central America (Honduras) Introduction Background of the case is the misuse one of the adhesives‚ Resistol‚ a toluene base glue‚ by the street o children of america‚ where the social economic were taken part of this situation. The resistol were produced by H.B Fuller company‚a global manufacture of adhesives‚ selalants‚ and other specialty chemicals‚ and had operations in over 40 countries in North America‚ Europe‚ Asia and Latin America. H.B Fuller 1994 total
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Synthesis and Structure of Alcohols Alcohols can be considered organic analogues of water. H O H R O H Alcohols are usually classified as primary‚ secondary and tertiary. H R H OH H primary R R OH R R OH OH R secondary tertiary phenol Alcohols with the hydroxyl bound directly to an aromatic (benzene) ring are called phenols. Nomenclature of Alcohols (Normally any compound’s name which ends in –ol is an alcohol of some sort) IUPAC rules that:
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Production of materials 1B – identify the industrial source of ethylene from the cracking of some of the fractions from the refining of petroleum Industrial source of ethylene (ethene) * Obtained from Crude oil – fractional distillation * Heated to high temps * Components vaporise and rise up tower where condense and collect * Lower the boiling point‚ higher up tower compound rises * Separates crude oil into fraction each with different boiling range - Catalytic Cracking
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Bromination of Trans-Cinnamic Acid Christopher B. Martin CHEM 3411 1 Mechanism of Bromine Addition to Alkenes Understanding the chemical mechanism (order of bonds broken and made as well as intermediates formed) has a great value in chemical synthesis. The chemical mechanism of a reaction will influence the rate of the reaction‚ the stereochemistry of the product(s)‚ and the extent of possible undesired side reactions. Organic reaction mechanisms investigate the path towards a desired product
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Abstract The bromination of trans-cinnamic acid was completed to determine dibromide’s stereochemical structure and its mechanism. After the addition of bromine to trans-cinnamic acid‚ the product was identified by its melting point and infrared spectrum resulting in erythro-2‚3-Dibromo-3-phenylpropanoic acid after comparing similar properties. Introduction In this lab‚ the bromination of trans-cinnamic acid was completed to determine dibromide’s stereochemical structure‚ and from there determine
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