budullewraagh

yeah, while the honours chem teacher is afraid of me, the ap chem teacher is so cool...perhaps thats because when i met her i asked to borrow the ap chem book so i could study for the exam. finished through page 200 the day i got it

polymerized tetrafluoroethylene perhaps? ok, GO HOME. we're not here to tell you how to blow things up, especially if you're some random kid who JUST showed up and didn't even confirm with the confirmation email.

i get respect from my peers my former chem teacher think i'm insane though and is somewhat afraid of me :\ is there ANYTHING i could add to my paper? is there ANYTHING i should change?

well, one example of a specific pH you need could be demonstrated by the inside of the mitochondria. you need a high concentration of hydronium cations so they will diffuse over the membrane via ATP synthase or else the electron transfer series will not work

well, im just saying. you can't know the molar mass if you don't know the formula. thus, if you're just given any sample of a hydrate and you don't know the potential hydrates, you cannot quantitatively solve this problem

-displacement reactions can be defined as either "single replacement" or "double replacement". an example of a single replacement reaction: 2KI(aq)+Cl2(g) --> 2KCl(aq)+I2(s) as you see, the chlorine displaces the iodide anion, oxidizing it to iodine and reducing to the chloride anion an example of a double replacement reaction: NaNO3(aq)+KCl(aq) -->NaCl(aq)+KNO3(aq) the most active anion is the nitrate and the most active cation is the potassium. upon distillation, one can find that NaCl and KNO3 are present. -sulfur dioxide is not very soluble. when it does dissolve some of it hydrolyzes to form sulfurous acid (H2SO3) much of which dissociates, not sulfuric (H2SO4). -nitric acid oxidizes metals. when any acid reacts with carbonates or bicarbonates, the following reaction occurs (let X=anion at -1 charge): Na2CO3(aq)+HX(aq)-->CO2(g)+NaX(aq)+H2O(l) Note: this works for any acid, monoprotic, diprotic, triprotic, tetraprotic etc.

if you don't have that you can't find the answer

mmm, banana oil...enrages bees... it isnt necessary actually. i take it you are doing the esterfication of isopentanol and acetic acid? they say they want an excess of acetic acid i believe because you want the hydronium cations as a catalyst. do it in the presence of another (prefferably mineral) acid and you'll be set

???what are the potential answers?

well...if you take for example, a sample of Al(NO3)3*9H2O there will be 9 water molecules per aluminum nitrate molecule

yeah no worries. a ctually this isn't getting graded. in fact it's not for a class. speaking of classes, im not even taking chem this year. i'm taking AP physics and AP bio and i'll be taking the AP chem EXAM at the end of this year and the actual class next year. i wrote this paper for apps for summer college

actually, as mentioned in my paper, calcium fluoride was used to lower the melting point of metal ores. fluorine was first used (as calcium fluoride) in this way. i have sources and it turns out that fluorine comes from the "flux" meaning of "fluere". thanks for your input though

yeah but i don't do nuclear...and i'm sane! and i actually speak to my parents. eek, rdx is crazy stuff man

it is finished. i would appreciate feedback if possible. if there is anything i could possibly add, let me know. without further adieu, i present my fluorine paper: One night in the Sarbonne region of France in the year 1886 Henri Moissan nervously prepared his apparatus. Having already spent a great amount of money on custom made parts, featuring a platinum U-tube, Moissan knew success was necessary to his professional career, if not his life. The skittish Moissan thought over the procedure of his experiment one last time. This could not fail he thought, a nagging doubt nonetheless in his mind as he turned on his direct current battery. Soon Moissan noticed a pale yellow gas appear at the anode. Success was indeed apparent after almost a century of constant experimentation. The tiger had finally been isolated. Fluorine (Latin, fluere, translation to "flux") always proved to be an elusive element. First isolated in 1886 by the French chemist Henri Moissan, fluorine was originally referred to as the "gas of Lucifer" and the great "tiger" of chemistry. Such names were true to its remarkable properties, which is what left fluorine as a mysterious, almost mythological element for decades, as most chemists chose not to attempt to isolate it for fear of death. In fact, many of the first chemists who isolated fluorine suffered significant physical harm, some of which proved fatal, as fluorine attacks the heart and bones rapidly. Fluorine has been mentioned in realistic fictional writings such as The Ernest Glitch Chronicles. In these writings, one can see the mystery this chemical proved to be in the years following its discovery. In a fictional letter written to Michael Farraday on July 8, 1856, Ernest Glitch wrote "Your concern about Hodges` health and employment exasperates me Faraday! However, in accordance with your wishes, I have reinstated him. I may say Faraday, that finding Hodges afforded me no end of trouble, and not inconsiderable expense. The wretch had travelled to Newcastle town moor, and was attempting to eke out an existence with a carnival show. Hodges` earning potential had recently plummeted, like a stooping peregrine, after an unfortunate incident involving the mayors wife. The carnival owner forbade him to further display his fluorine scars, and his electrical scarification is hardly of the shocking nature lucifers gas, the tiger of chemistry, had afforded him. He is still maintaining blindness in one eye, and I have had to reduce his previous workload because of frailness." Fluorine was always considered to be a remarkable element, even in its salt forms. In 1529, Georgius Agricola discovered that fluor lapis, (now known as fluorspar or CaF2) with its low melting point of 1403 Celsius could be used as a flux to lower the activation energy of the melting of ores for smelting. One and a half centuries later in 1676, it was found that flux, when heated on a metal plate, shines with a blue-white luster. This would later be found to be a result of catalytic action of the fluoride anion on ozone, which causes colourless diatomic oxygen to oxidize to the pale blue ozone (O3) molecule. At about the same time, a glass cutter found that heating fluorspar with strong acids created agents that etched glass. In 1771, Carl Wilhelm Schelle discovered hydrofluoric acid (HF) after heating fluorspar with oil of vitriol (sulfuric acid, H2SO4). Schelle also found that this acid was capable of dissolving glass and silaceous earth. In discovering this acid he helped Humphry Davy disprove Antoine Lavoisier’s theory that all acids contain oxygen. André-Marie Ampère proposed to Davy that the acid must contain hydrogen and a new undiscovered element. In the experimentation the ensued, Davy, Joseph Louis Gay-Lussac and Louis Thenard suffered greatly from inhalation of the acid vapours which predominantly attack the heart and bones. The Reverend Thomas Knox and his brother George made an apparatus with fluorspar. The Reverend barely escaped with his life and George was bedridden for three years before he regained his health. Paulin Louyet of Brussels, Belgium nonetheless continued his experimentation and died, as did Jérôme Nicklès of Nancy, France. Edmond Fremy attempted to replicate Louyet’s experiments but instead of using hydrated fluorspar he electrolyzed anhydrous fluorspar. Unfortunately, the gas produced at the anode reacted instantly. In 1869 George Gore produced a small amount of fluorine through electrolysis. Unfortunately for Gore, he had not realized that fluorine would react explosively when combined with hydrogen and the two gases produced at opposite electrodes exploded violently. Gore narrowly escaped injury. Fluorine was not successfully isolated until 1886 when Ferdinand-Frédéric-Henri Moissan, a student of Fremy’s successfully electrolyzed dry potassium acid fluoride in anhydrous liquid hydrogen fluoride in a platinum U-tube using platinum-iridium electrodes using methyl chloride to cool the apparatus to -50 Celsius. Although an advocate of extreme cleanliness in his laboratory, Moissan was subjected to fluorine poisoning many times and died prematurely as a result. For one to understand the dangers and true beauty of fluorine, one must consider its remarkable properties. Fluorine, element number 9, has the greatest electronegativity of all elements according to the Pauling scale as well as the Allred-Rochow scale. According to Linus Pauling, electronegativity can be defined as the relative attraction of an atom for the valence electrons in a covalent bond. It is proportional to the effective nuclear charge and inversely proportional to the covalent radius. Pauling’s electronegativity formula is as follows: X=(0.31(n+1+or-c))/r+0.50 where the variable "n" represents the number of valence electrons, "c" represents any formal valence charge on the atom, where the sign before it corresponds to the sign of this charge and "r" represents the covalent radius in angstroms. One can easily calculate the electronegativity of fluorine using Pauling’s formula: X(F)=(0.31(7+1-1))/0.64+0.50 X(F)=3.890625 Pauling realized that because electronegativity is not concerned with atoms in isolation, but rather atoms in molecules, it is not possible to define precise electronegativity values. All of Pauling’s figures were based on bond energy data measured using heats of dissociation and formation. It was because of the lack of precision of electronegativity values that Pauling originally gave fluorine an arbitrary electronegativity of 4.0. For cations, however, this formula has proven to be less than accurate. A new formula was proposed for the electronegativity of cations: X=0.44(phi)-0.15 where (phi) represented the work function, or the energy necessary to remove an electron from the metal surface in thermoelectric or photoelectric emissions. According to this formula, the electronegativity of calcium is equal to 1. According to Pauling’s formula, X(Ca)=0.31(2+1+2))/1.74+0.5 X(Ca)=1.390804598 Now, considering fluorine’s electronegativity, one can understand how fluorspar is able to catalyze the oxidation of diatomic oxygen to ozone. According to the Gordy formula, the degree of ionic character is equal to the absolute value of the difference of the electronegativities of bonded atoms divided by 2: DIC=|Xa-Xb|/2 DIC=|3.890625-1.390804598|/2 DIC=1.249910201 More accurately: DIC=|3.890625-1|/2 DIC=1.4453125 A more sophisticated formula was proposed by Hannay-Smyth: DIC=0.46*(|Xa-Xb|)+0.035*(Xa-Xb)^2 DIC=0.46*(|3.890625-1|)+0.035*(3.890625-1)^2 DIC=4.254187012 Calcium fluoride proves to be very ionic, and at high temperatures proves to be even more ionic due to the increased rate of collisions between molecules. The bond stretching force constant for stable molecules exhibiting their normal covalencies can be estimated (in units of 10^5 dynes per cm^-1) by the formula: K=1.67N((XaXb)/D^2)^(3/4)+0.3 where "N" represents the bond order and "D" represents the internuclear distance in angstroms. K=1.67*1((3.980625-1)/(.64+1.74)^2)^(3/4)+0.3 K=1.331766779 These extreme numbers are simply numerical representations of the physics of the fluorine atom. It is the combination of these physical properties that gives fluorine its characteristic bonding abilities. Fluorine is atomic number nine and has a valence shell containing two electrons in its 2S shell and five electrons in its 2P orbital. Because its valence shell is only one electron short of satisfying the octet rule, there is the maximum possible number of protons present before the electrons must be placed significantly farther away in a 3S orbital (disregarding the inert gas neon). With covalent radius of 64 picometers, fluorine is quite small compared to other halogens. The radii (in picometers) of chlorine, bromine and iodine, respectively, in a diatomic molecule are 99, 114.2 and 133.3. Despite the fact that chlorine has more protons than fluorine, bromine has more protons than chlorine and iodine has more protons than bromine and the fact that the effective nuclear charges of the halogens increases down group 17, the protons lose their attractive force and control over the increased distance from the nucleus to the valence shell, leaving fluorine as the element with the greatest forces to attract electrons. This property is clearly evident in its reduction potentials which are, (in E^(theta)/V): F2 __2.866__ F-(aq) F2 __2.979__ HF2- F2 __3.053__ HF(aq) as well as its ionization energies (in kJ/mol^-1) the first of which is 1,681. These atomic and valence properties give fluorine its remarkable bonding properties. Such properties made fluorine remarkably difficult to isolate during the early years of its experimentation. When pumped into an ionic aqueous solution, fluorine will displace any anion, sometimes resulting in decomposition of this anion. Examples can be demonstrated by the following reactions: F2(g)+2NaCl(aq)à2NaF(aq)+Cl2(g) F2(g)+2KMnO4(aq)à2KF(aq)+2MnO2(s)+2O2(g) While completely dry fluorine cannot attack completely pure amorphous silicon dioxide, it is almost impossible to completely dry fluorine and eliminate impurities in glass. As a result, there are multiple ways in which fluorine is able to self-catalyze. If the fluorine is wet at all, it hydrolyzes somewhat to form hydrogen fluoride, which attacks glass. If the fluorine is dry, it finds impurities in the glass, which ideally has the tetrahedral structure: O O O | | | O-Si-O-Si-O-Si-O | | | O O O | | | O-Si-O-Si-O-Si-O | | | O O O Of course, this is not a possible structure, as all of the oxygen atoms bordering the outside of the structure are lacking one bond. The above would be more similar to the quartz lattice structure of silicon dioxide than glass. Glass itself is an amorphous solid, which contains various impurities. One example of an impurity is SiO(OH)2. While dry fluorine is not capable of attacking a double bond between silicon and oxygen, it is able to attack the hydroxyl radicals which are repelled by the doubly bonded oxygen, which is situated 1.7595 angstroms away form the silicon atom. Because it is so far away from the silicon, the doubly bonded oxygen does not effectively repel fluorine as it attacks the silicon and hydroxyl radicals. Diatomic fluorine immediately forms hydrogen fluoride on contact with the hydroxyl radicals. The oxygen of the hydroxyl radicals, having lost a bond, instantaneously bonds together and is displaced by the hydrogen fluoride, forming SiOF2H2 as an intermediate and O2 which is immediately attacked by more fluorine to form gaseous tetrahedral SiF4 and H2O. The water produced hydrolyzes fluorine to form yet more HF, which directly attacks even pure silicon dioxide. In this reaction, hydrogen bonds to oxygen and fluorine bonds to silicon (4HF+SiO2àSiF4+2H2O). Other products and intermediates of these reactions are tetrafluorosilicic acid and hexafluorosilicic acid. The ability of fluorine to attack many oxidized compounds has proven to be quite useful in the way it is able to amplify certain properties of some compounds. While sulfuric acid (H2SO4) is a very strong acid (pKa1=-3, pKa2=1.99) fluorosulfonic acid (HFSO3) is approximately 10,000 times stronger (pKa=-8.60). The ability of fluorine to increase dissociation in polyatomic anions can be best demonstrated by pentafluoroantimonic acid (HF:SbF5). Hydrofluoric acid alone is considered a weak acid, with a pKa of 3.20. When mixed in a solution with antimony pentafluoride however, the HF dissociates almost completely to form H+ and SbF6-. In this situation, the fluorine completely takes control of the hydrogen’s only atom and forms a coordinate covalent bond with the antimony pentafluoride, leaving the hydronium cation behind. When fluorine makes a covalent bond, it is likely to keep this bond and as a result, the equilibrium of this reaction almost exclusively favors the forward reaction. Toothpaste companies have capitalized on this property. While analyzing the enamel of elephants’ teeth in 1802, Domenico Pini Morichini found much calcium fluoride along with the predicted predominant presence of calcium phosphate. Bones are composed primarily of hydroxyapatite (Ca2(PO4)3(OH)). When in contact with the fluoride anion (in the form of aqueous sodium fluoride), the hydroxyl radical is displaced by fluoride which makes an even less soluble compound known as fluoroapatite. By fluorinating one’s teeth, one can prevent the corrosion of enamel, which is normally slightly susceptible to attack by strong acids. Chlorofluorocarbons (CFCs) were synthesized for use in refrigeration devices. These compounds were formed of one to two carbon atoms bonded with fluorine and some chlorine. While almost completely chemically inert, CFCs were found to be quite hazardous for the atmosphere if released. Ultraviolet rays from the sun were able to remove the chlorine from CFCs, one molecule of which could catalyze the decomposition of millions of ozone molecules in seconds. The fluorine however, is bonded so strongly to carbon that it cannot be removed by such rays. Another strong covalent fluorine compound is polytetrafluorethylene (PTFE), which has the formula (C2F4)n. The carbon in tetrafluoroethylene is SP^2 hybridized, with 120 degree bond angles. In polymerized tetrafluoroethylene, the carbon becomes SP^3 hybridized, forming 109.5 degree bond angles. With perfectly uniform highly negative fluorine strongly bonded to a long carbon backbone, polytetrafluoroethylene is not only practically chemically inert, but it also has a remarkably low Mu coefficient of friction with other PTFE, which happens to be 0.04. Considering the fact that friction is not actual contact between matter, but rather the conflict between repelling forces, the fluorine atoms of PTFE do not touch one another, and are rather passed, one slightly apart from the other, as they move, with the perfectly uniform PTFE molecules only forming slight "bumps" between one another in a perfectly symmetrical structure. Fluorine does indeed make strong covalent bonds, but it also makes somewhat weak covalent bonds with the lower "inert" group 18 gases. Such compounds as krypton difluoride are formed by pressurized fluorine and krypton gases. This compound hydrolyzes in water, forming hydrofluoric acid and krypton gas or, depending on pressure, K8(H2O)46, a clathrate complex of krypton. Much more experimentation of the action of fluorine on xenon has been documented. Such compounds made from xenon and fluorine are XeF2, [XeF]+[AsF6]-, XeF4, XeOF4, XeO2F2, XeF6 and XeO3F2. All fluorinated xenon compounds are strong oxidizing agents and most hydrolyze to form hydrofluoric acid or a lower xenon fluoride as well as xenon (and xenon clathrate complexes depending on pressure), and/or the corresponding xenon oxide. While fluorine tends to make strong covalent bonds, it also forms some unstable ionic bonds. Fluorine nitrate and permanganyl fluoride are incredibly unstable almost mythical compounds used as rocket propellants. There is almost no information on the latter, but the former has been reasonably well documented. Formed from the very negative nitrate anion and fluorine, the most negative element, the union of these two compounds is broken remarkably easily and it decomposes to form diatomic oxygen, nitrogen dioxide and fluorine gas. Fluorine, the most negative element in existence and the most negative element conceivable, truly lives up to its title of "gas of Lucifer". With self-catalytic properties, the ability to displace any aqueous anion and the ability to form particularly strong covalent bonds, fluorine is unique and capable of amplifying the properties of many compounds. These properties have fascinated many and resulted in the advancement of society.

pssh, what are parents for? i tell mine what the chems are that i'm buying, what i'll do with them, how i'll store them and they're ok with it

eek, methanol instead of ethanol? sounds deadly

ah, so N2(l) i read it again...whoops i still dont think it's accurate. (aq) means aqueous, or dissolved in water. he meant (l) which means liquid.

man that's awful. they sell to the hobbyist? i can see some lunatic ordering a few tons of KNO3 and heading towards junk yards to find old car batteries...

aqueous nitrogen???

ah i see. prices are ok then i suppose, altho some are really bad. it's a shame the dollar is so weak now

thats great altho i have no idea how expensive the chems are. the "pris" is in "i SEK" units. do you know the conversion factor?

nah, i'm not that stupid. plus i wouldnt waste sulfuric on organic peroxide synths...i'd just use 35% hydrochloric from drain cleaners. on second thought, that would be quite a sight, seeing my peroxide and sulfuric mix together...peroxymonosulfuric acid, anyone?

mods, dont hate me if this wasnt a good idea to post, but i thought it would be good to post a bunch of good sites to buy chems from. i've found that hobbyist sites are good, but some reagents of equal quality you can buy for much less at photography stores. pottery and ceramic sites aren't too bad either, but generally you can get similar items at photography stores if you happen to know of any other sites, list them below with some information about them if you wish. Pyro/Hobbyist Sites: http://www.unitednuclear.com ^high quality acs grade chems. rapidly growing so check every few weeks as they will probably have more chems. best thing about this site is they sell some uncommon catalysts and you can buy 2oz of a wide variety of chems for not too much. $7.50 flat shipping rate with no extra charges for hazmat. ideal for smaller orders. http://www.skylighter.com ^pyrotechnics supplier. really low prices on powdered metals and oxidizers. they sell in "bulk" (usually by the pound or more). compared to unitednuclear, their prices on aluminum powders and dust as well as magnesium and such oxidizers as potassium nitrate and barium chlorate are incredibly low. http://www.kno3.com ^good shipping policies. they sell some uncommon items, such as potassium persulfate, calcium, sodium and potassium metal, but in addition they sell red phosphorus. yes, high quality pure red phosphorus, and it's not too expensive either (100g for £19.50). their potassium perchlorate is absurdly expensive, but their potassium permanganate, potassium chlorate, iodine, and aluminum powder are quite reasonable. http://www.al-chymist.com ^they have some really nice discounts (i got 25g of sodium peroxide for $5), but they charge $25 for hazmat and then shipping, which tends to be expensive as well. Photography Sites: http://www.artcraftchemicals.com/ ^they sell some abstract chems like chloroauric acid, cesium chloride and palladium chloride. http://www.bostick-sullivan.com/main/index.htm http://www.silverprint.co.uk/ http://www.raycochemicals.f9.co.uk/ ^cheap iodine...altho the place looks like it will be sold very soon so i'd be careful with orders if i were you Other Sites http://www.uspigment.com/ ^cheap oxides and salts by the pound

ive actually had ice cream made that way before. it's incredibly good and far better than normal ice cream...altho liquid nitrogen is significantly more expensive to keep cold

the C=C bonds cause a bent shape btw