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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Acid rain is considered precipitation in the form of rain‚ snow‚ or fog. It is not regular precipitation. It is precipitation that is polluted by acid. Emissions of sulfur dioxide and nitrogen oxide into the atmosphere cause this precipitation to become acidic. These emissions are released into the atmosphere by human activity‚ such as automobiles‚ industries‚ and electrical power plants that burn fossil fuels like coal and oil. When these gases are released‚ they mix with water vapor in the clouds
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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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Lauric Acid Lauric acid‚ also known as Dodecanoic Acid‚ was discovered in 1849 by Marrsson T. It was first discovered in Lauraceae seeds‚ but it is also commonly found in soaps‚ vegetable oil‚ coconut oil‚ and breast milk. Lauric Acid is a clear‚ solid compound that is insoluble in water. It also comes in the form of a white powdery substance. The chemical formula is C12H24O2. It has a molecular weight of 200.32 g/mol. Lauric Acid also has a melting point of 44 C and a boiling point of 289.9
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of Shikimic Acid‚ intermediate for the production of Oseltamivir‚ the Avian Flu drug Supervised by: Dr. Reza Yegani Dr. Mohammad Hossein Sarrafzadeh Mr. Habibollah Ramezanzade by: Kaveh Yazdifard Presented on: 1385/10/3 Contents Acknowledgement Introduction Shikimic Acid & its Natural Properties Derivatives of Shikimic Acid Avian Flu Sickness‚ Medications Oseltamivir and Shikimic Acid’s Role in Synthesis Production of Shikimic Acid Extracting Shikimic Acid from the Plant
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Suggested time allotment: 5 to 6 hours MODULE 2 ACIDS AND BASES In Module 1‚ you identified common properties of solutions using different methods. You learned how to report the amount of the components in a given volume of solution. You also found out that not all solutions are liquid. Some of them are solids and others are gases. Towards the end of the module‚ you investigated the factors that affect how fast a solid dissolves in water. Most of the solutions you studied in Module 1
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Jennifer Everett Phase 4 DB Instructor: Clement Yedjou 3/10/2015 Acid rain Acid rain is a result of air pollution that is harmful to the environment‚ generally caused by fuels being burnt. When any type of fuel is burnt‚ many different chemicals are produced. These gases that are released react with the water in clouds‚ and the rain from these clouds is acid rain. This type of acid disposition can appear in many other forms besides just rain‚ such as sleet‚ snow‚ and fog (Editorial Board‚ 2013)
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Acid Rain and the Effects of our Monuments and Churches The two controlled experiments that I chose to do‚ do not involve trees or plants‚ which I think a lot of people will be doing. I wanted to explore the devastation that acid rain does to our historic monuments and beautiful churches. My first controlled experiment is based on the Statue of Liberty. It is made of copper so I am using pennies in my experiment. (nps.gov. n.d.) My observation is that acid rain corrodes metals
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alcohol‚ triphenylmethanol. The purity of the final product will then be considered by melting point and IR spectroscopy. Final purified triphenylmethanol weighed 8.02 grams and melted at 158.5-162 degrees Celsius. Introduction: Grignard reagents are the most useful way to form primary‚ secondary or tertiary alcohols from a carbonyl group. The Grignard reaction involves the nucleophilic addition of an organomagenesium complex to a carbonyl carbon followed by acid work-up. This reaction involves
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dielectric constant and dielectric loss were measured within the frequency range from 10 Hz to 106 Hz and the temperature ranging from 50°C to 300°C. The results showed that the dielectric constant and dielectric loss of the sample are frequency dependent and temperature dependent. Dielectric constant and dielectric loss increases with decreasing frequency and increasing temperature due to interfacial polarization. Introduction: Dielectric materials with high dielectric constant‚ good thermal
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