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College Chemistry I PHS 1025 Fall 2012 Practice Exam 3A
College Chemistry I PHS 1025 Fall 2012 Practice Exam 3A

... MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. 1) Balance the chemical equation given below, and determine the number of grams of MgO needed 1) _______ to produce 15.0 g of Fe2O3. ___ MgO(s) + ___ Fe(s) → ___ Fe2O3(s) + ___ Mg(s) A) 11.4 g ...
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... has the lowest possible number. • Number the other substituents on the carbon chain. • An italic “N” is used as a prefix for a substituent on nitrogen. Examples: ...
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... g. Which one of the following will always DECREASE the amount of O2 dissolved in water? increasing the temperature and increasing the pressure of O2 above the water increasing the temperature and decreasing the pressure of O2 above the water decreasing the temperature and increasing the pressure of ...
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... • In step 1, the nucleophile attacks an electron-deficient carbon, thus cleaving the C—O bond and relieving the strain of the three-membered ring. • In step 2 the alkoxide is protonated with water to generate a neutral product with two functional groups on adjacent atoms. • Common nucleophiles that ...
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... form. The crystals have six water molecules for each unit of cobalt chloride. The formula for this compound is CoCl2 • 6H2O. The compound’s name is cobalt chloride hexahydrate. The prefix hexa- means “six,” so hexahydrate means “six waters.” You can remove water from these crystals by heating them. ...
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... the highly exothermic enthalpy change of hydration by water. (ii) Inorganic by-product : Br2(g) + SO2(g) NaBr + H2SO4 à NaHSO4 + HBr 2HBr(g) + H2SO4(l)  Br2(g) + SO2(g) + 2H2O(l) Organic by-product: But-1-ene CH3CH2CH2CH2OH à CH3CH2CH2C=CH2 + H2O It was expected that candidates would consider the w ...
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... For the chlorinated derivatives of enthanol (ClCH2CH2OH, Cl3CCH2OH), the inductive electron-withdrawing effect of the local halogens enhances the acidity of the parent alcohols; this effect is additive, with trichloroethanol being more acidic than chloroethanol and ethanol. Phenol (an aromatic ring ...
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Organosulfur compounds



Organosulfur compounds are organic compounds that contain sulfur. They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin. Nature abounds with organosulfur compounds—sulfur is essential for life. Of the 20 common amino acids, two (cysteine and methionine) are organosulfur compounds, and the antibiotics penicillin (pictured below) and sulfa drugs both contain sulfur. While sulfur-containing antibiotics save many lives, sulfur mustard is a deadly chemical warfare agent. Fossil fuels, coal, petroleum, and natural gas, which are derived from ancient organisms, necessarily contain organosulfur compounds, the removal of which is a major focus of oil refineries.Sulfur shares the chalcogen group with oxygen, selenium and tellurium, and it is expected that organosulfur compounds have similarities with carbon–oxygen, carbon–selenium and carbon–tellurium compounds, which is true to some extent.A classical chemical test for the detection of sulfur compounds is the Carius halogen method.
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