Contents 1) Sulphuric Acid----------------------------------------------------------------(1-6) a. Uses of sulphuric b. Manufacture of sulphuric acid c. Sulphur dioxide and environmental pollution 2) Ammonia and Its Salt-----------------------------------------------------(7-10) d. Uses of ammonia e. The properties of ammonia f. Manufacture of ammonia g. Preparation of ammonium fertilisers 3) Alloys------------------------------------------------------------------------(11-14)
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Atmosphere –Water Interactions C. P. Huang Stumm W. and J. J. Morgan. Chapter 5. Aquatic Chemistry 1 Environmental Systems 2 5.2 Atmospheric generation of acidity 3 Genesis of acid rain 4 Chemical processes and Chemical Composition of Water Droplets 5 uM ueq/L NO360 60 SO4244 88 Cl 25 25 S(X) 173 Mg2+ 4.5 9 Ca2+ 16 32 NH4+ 85 85 K+ 2 2 Na + 5 5 H+ 50 50 S(M) 183 CH3COOH 5 5 6 7 8 Total Annual
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Hexagon: Cyclohexane ISO Isopropyl- a side chain off of the main chain that has a duel end -< Isobutyl- \/< Isopentyl- -/\< Aromatic Hydrocarbons: Doesn’t react like an unsaturated molecule. Ortho- Meta- Para- Toluene- Phenol- Addition Vs Substitution: Substitution reactions occur when molecules contain saturated chains (No double or triple bonds) or
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Question 1 Motor vehicles in Malaysia are increasing rapidly nowadays. Almost every household have at least 2 cars and a motorcycle. It shows that Malaysians lifestyle also increasing. But from 1980 till 2010‚ the statistics of motor vehicle theft are increasing. Statistics shows that it increased year by year. The graph shows that from year 1980 till year 1995‚ the number of cases is still maintained. But‚ starting from that year till 2010 increased rapidly. The green line that indicates all
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Name Lab Section GTA Station # 5. Extraction Pre-lab questions Complete the following questions and submit before beginning the experiment. 1. Which layer will be the aqueous layer when using dichloromethane (methylene chloride) as the solvent (i.e.‚ top or bottom)? Which layer will be the aqueous layer when using ether as the solvent? 2. When everything has been separated in Part D‚ which compounds will be in test tubes 1‚ 2‚ and 3?
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Keystone Pipeline Project The United States is a fossil fuel hungry nation whose economy‚ markets‚ and transportation is highly dependent on the abundance of crude oil and petroleum. Although there is roughly 85.9 billion barrels of undiscovered technically recoverable crude oil currently in the form of oil shale located beneath our soil‚ we still rely on imports from foreign countries. With a crude oil and petroleum product net import of 7‚270 thousand barrels per day the United States is one
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4 3 Material Safety Data Sheet Acetaldehyde MSDS Section 1: Chemical Product and Company Identification Product Name: Acetaldehyde Catalog Codes: SLA1309 CAS#: 75-07-0 RTECS: AB1925000 TSCA: TSCA 8(b) inventory: Acetaldehyde CI#: Not applicable. Synonym: Ethyl Aldehyde; Ethanal; Acetic Aldehyde Chemical Name: Acetaldehyde Chemical Formula: CH3CHO Contact Information: Sciencelab.com‚ Inc. 14025 Smith Rd. Houston‚ Texas 77396 US Sales: 1-800-901-7247 International Sales: 1-281-441-4400 Order Online:
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Fall 2013 Drug Ed Exam 2 The use of cocaine by members of the general public in Europe was initially in the form of coca powder. pills. drinks‚ such as coca wine. cigarettes. Dr. W. S. Halsted‚ the "father of American surgery‚" experimented with cocaine’s ability to produce dependence. a deep sleep. psychosis. local anesthesia. Which famous physician studied cocaine as a treatment for morphine dependence and depression? Benjamin Rush Sigmund Freud Johns Hopkins Parke Davis
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spectroscopy. The unknown ketone is from a homologous series of methyl ketones. CH3CO (CH2) nCH3 The first step in the lab is the preparation of the solvent used in the developing chamber for thin layer chromatography. The solvent used is a 3:1 mixture of toluene and petroleum. After the developing chamber is prepared‚ it is essential to begin preparation of the unknown DNPH derivative[6]. The preparation of the 1‚2 DNPH derivative of a ketone is in fact a small organic synthesis which produces a fraction
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An early observation of fluorescence was described in 1560 byBernardino de Sahagún and in 1565 by Nicolás Monardes in theinfusion known as lignum nephriticum (Latin for "kidney wood"). It was derived from the wood of two tree species‚ Pterocarpus indicus andEysenhardtia polystachya.[2][3][4][5] The chemical compound responsible for this fluorescence is matlaline‚ which is the oxidation product of one of the flavonoids found in this wood.[2] In 1819 Edward D. Clarke[6] and in 1822 René Just Haüy[7] described
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