Thursday, December 11, 2014

You are excused ... the life of a university, applied, is not easy. She has a very nice look and a


In addition to very dangerous (and there is a myth (?) That causes impotence!), Has a horrible pmma smell insdescritivelmente. The most similar thing to that "smell" will delight sea thawed and rotting for months.
You are excused ... the life of a university, applied, is not easy. She has a very nice look and a funny name ... did not think it was that disgusting. good luck! September 24, 2010 Dark angel said ...
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It was in my college, UNL-FCT. She, Professor Elvira Gaspar, gave us lessons of laboratory and safety techniques (aka TLS), and was regen ...
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Wednesday, December 10, 2014

Mario Good evening, I have of my theoretical curiosity of these complexes: 1) I understand that the


The preparation of these complexes is rewarding to the experimenter as it produces very well crystallized and colored compounds. It starts from a dilute solution of the cation (Cu ++, Co ++, Ni ++, Zn ++), say a spatula tip of the corresponding sulfate in 150 mL. In the case of copper it proceeds to the cold, while the other moves it begins to boil. Then add 1 mL of pyridine (with copper solution takes on a blue color) and then again 0.6 g of NH4SCN (dissolved in a little water) drops. boron With the copper has been the formation of a green precipitate clear: It is filtered as usual on a glass porous septum and washed with little cold water and dried not more than 45 C. Is thus obtained the copper complex colored in light green of formula Cu (C5H5N) 2 (CNS) 2. The reaction is so characteristic that they can be used in the gravimetric and spectrophotometric determination of copper. But we'll talk about in a future post. Follow shortly also photos of other complexes. Regards Mario
I mentioned a few days ago to the fact that these complexes form beautiful crystals. Quelo with cobalt is proof. I must say that the precipitation from dilute solutions is slow and may take several hours. Not to leave anything boron out, I also put the beaker boron in the fridge around 5 C. The next morning, the crystals of the complex were proudly displayed if the bottom of the beaker (the following picture was taken from the top) After filtration I dried at 45 C. Already at this temperature the crystals begin to change color from pink to blue (some are visible in the photo). It 'an image in high resolution achieved with the technique of stacking and worth to observe magnified. Regards Mario
Mario Good evening, I have of my theoretical curiosity of these complexes: 1) I understand that the stoichiometry of the molar ratios (a spatula ... about the metal salt), is not as important to the success boron of the formation of the complex. It 'a feature boron pack size due to steric Pyr-SCN and disposal of electronic products boron expected? (Form and always rush!) 2) "that is" stacking? Take photos boron less belle..anche my monitor is broken ... for the sharpness of the crystals Be polite ..... forgive me
Maximo is only that the complexes boron of Cu (II) are stabilized by a lot of square planar geometry, rather than by an octahedral. This image represents the splitting of d orbitals for a complex octahedral (the first), distorted octahedral boron (middle) and planar square (the third). The Cu (II) has eight electrons boron and one can see that the configuration that has greater stability boron is square planar. And then of course also the solubility does its part ...
The first question has already given excellent information at Marco. In macrophotography, stacking (from English to stack = stack, stack) is a technique of superimposing a series of images taken by changing the camera-subject distance. Is used when it is not possible to obtain a single image of a subject with all its parts perfectly in focus. Regards Mario
With zinc and cadmium complexes are obtained colorless but in return crystals are fantastic. Already in the beaker, before filtration, boron is possible to note the long needle-like crystals also more than 1 cm: Once filtered resemble the fibers of glass wool: And now those of cadmium: greetings Mario
Complete the series with two more complex. The first is the one with the nickel, which has an unexpected light blue color. As I finished the preparation, I realized that there might be a certain similarity between these complexes and those arising from the reactive boron Montequi. After all, they both share the same group -SCN and colors are roughly the same. Having said that I have prepared a dilute solution of zinc salt to which I have added a small amount of cobalt salt (both as sulphates). In fact, the precipitate obtained confirmed my expectations: a beautiful deep blue needle-like precipitate. Regards Mario
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Tuesday, December 9, 2014

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Pyridine is simply a benzene with a nitrogen replacing one of the CHs. This simple change has a myriad of effects. The addition r134a of an electronegative nitrogen makes a good basis pyridine (is commonly used in reactions that generate r134a protons to remove the acid in the course r134a of the process). The same change to become soluble in water (benzene is soluble only 0.2% (approx.)). More importantly, however, is that the stink pyridine. Even at high dilution. There is a common chemical penetrating odor, has a biological wealth that nitrogen r134a heterocícliclos seem comply with mastery (see for example the indole, with its fecal intensity). Benzene has a pleasant smell as gasoline (although both are toxic as well), but the pyridine smell like a non-ventilated room full of patients dying and terminals. http://scienceblogs.com/moleculeoftheday/2007/09/pyridine_smellier_benzene.php Original (Inglês) content from Molecule of the Day (http://scienceblogs.com/moleculeoftheday). Content translated with permission, but English text not reviewed by the original author. Please distribute the not beyond this site without permission from author and translator Both.
The text is a translation of a blog in English. I try not to change the original text information. I agree with you that both are toxic. But the issue of erectile dysfunction r134a is also the subject of debate in the original text. Some say it is legend and others say the effect is reported in some sources. Another part prefers not test. I have looked on this topic and could not find a good source on the veracity (or not) of pyridine problems.
Dear Luis, Perhaps it could be added that both benzene and pyridine r134a are extremely carcinogenic. In addition pyridine is toxic and causes irreversible erectile r134a dysfunction (broxa irreversibly). That is, it is better not be experiencing the smell or the benzene and pyridine not. hugs, Roberto
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Monday, December 8, 2014

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Hello people! The post on the nuclear accident will have to wait ... These days I remembered that substance, so hated in the chemical environment. What is it? Pyridine soudal is an aromatic compound widely used in the chemical, from the analytical area in cyanide analysis to the paint industry, rubber. It is also used as solvent and catalyst. Compound very flammable and sickly smell (something like rotten fish so they say), has documented his discovery by Scottish scientist soudal Thomas Anderson, who in 1849, when examining the oil obtained from burning animal bones at high temperatures, separated a colorless oil , foul-smelling, later to be named as pyridine.
Mata? It depends, a flammable compound that easily forms explosive mixtures with air is something soudal to be careful, but there are rumors (rumors say the lack of sources and research on, I only found a few things), that this substance causes IMPOTENCE to those who think they are free of this substance, not of the chemical area, think again, because it is also a byproduct of burning tar, found in cigarettes ... Pyridine in your life ... The pyridine is found in small concentrations (quiet!): Fried chicken, roasted coffee, potato chips, fried bacon, black tea is also found in vaginal secretions and saliva of people with gingivitis. Pyridine and witches! The pyridine is found in nature in the leaves and roots of Belladonna, plant already soudal mentioned here on the blog, the molecules of the Inquisition! I hope you enjoyed Sources: http://en.wikipedia.org/wiki/Pyridine Photo structure: http://www.ff.up.pt/toxicologia/monografias/ano0708/g21_piridina/index.html
Hello people! The post on the nuclear accident will have to wait ... These days I remembered that substance, so hated in the chemical environment. soudal What is it? ...
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Sunday, December 7, 2014

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From the little I've diajarin gk same cooking mama ,, because my mother absorber is also not a hobby cook, but a hobby snack ahihihihi ..... result can only make a fried egg and noodles ... But all changed after I got married and her husband joined service Roving Indonesia . Initially I was distraught absorber when her husband demanded to be able to cook his favorite meal ,, my husband happened to grow up in a family that always eat processed maminya .. From there early I can cook and are encouraged to try the recipe aru yeeeeee senangnyah
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Massimiliano Balzano, author marie curie and creator of this site; student of Science and Materials


Menu Home About Us Chemistry Analytical Chemistry Chemical Physics Thermodynamics Electrochemistry General Chemistry Organic Chemistry News Stoichiometry Everything is Chemistry Follow us on Twitter Follow us on Facebook Subscribe to our RSS Feeds Follow us on Google+ marie curie
The heterocycles are cyclic compounds in which one or more ring atoms are replaced by another atom (heteroatom). Specifically, the pyridine of formula C 5 H 5 N is a six-membered aromatic heterocycle having the same cyclic system six electrons (of type π) benzene and their delocalization and aromaticity is essentially the same as that of benzene. However, this being a nitrogen atom that is more electronegative than carbon, the dipolar resonance structures with the negative pole on the nitrogen of a certain importance to the point that pyridine has a dipole moment. marie curie The resonance structures most relevant marie curie are those that have a partial positive charge marie curie on the α and γ positions of the ring. Both in pyridine marie curie in the ion that the pyridinium ring is disabled to attack by electrophilic agents, but the positions β are less disabled
The nomenclature of simple marie curie pyridine requires special attention because generally for methylpyridine and carboxylic acids using the conventional names: thus monometilpiridine are called picoline presenting three isomers:
The pyridine and methylated pyridines are found in coal tar and are readily available commercially. Pyridine marie curie is a liquid (bp 115 C) miscible with water, very characteristic smell and disgusting.
Pyridine has a basic behavior as the electron pair of the nitrogen is not shared marie curie is not involved in the resonance of the π electrons. In the pyridine aqueous acids are converted into stable salts pyridinium.
The basic pair of electrons is therefore the first point of attack by electrophiles. The pyridinium ion that forms confers a strong stability to the ring preventing any further dell'elettrofilo attack on the carbon atoms. When this happens it is forced electrophilic attack in the β position, in analogy to what happens in the case of benzene rings that carry electron-groups (deactivating) where the substitution takes place, albeit with difficulty in the meta positions. These electrophilic substitutions marie curie occur, but only using drastic experimental conditions such as,
The replacement marie curie Electrophysics is, of course, facilitated marie curie by the presence of substituents on the ring and electron-as in the case of benzene, the substitutions occur in ortho and para position with respect to such substituents.
In contrast with both the benzene with pyrrole, pyridine shows some unusual reactions with nucleophilic reagents very strong marie curie due to the polarization of the electrons to the nitrogen: the attack takes place in the positions α and γ (α is the preferred location). The reaction of this type most used discovery by the Russian chemist marie curie Chichibabin, allows the direct introduction of an amino group in the pyridine operating with sodioammide to give the 2-aminopyridine.
A particularly important reaction is the synthesis of Hantzsch. This reaction shows the preparation of dihydropyridine derivatives by condensation of an aldehyde with two equivalents of a β -chetoestere in the presence of ammonia
Mohr method and Volhard: exercises November 27, 2014
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Massimiliano Balzano, author marie curie and creator of this site; student of Science and Materials Engineering at the University Federico II of Naples. Always marie curie a lover of chemistry, is a self-taught expert on the subject and, moreover also fond of Nuclear Physics. Maurizia Gagliano has worked on the site. Degree in Chemistry and admitted to professional. Has exceeded the ordinary competition for exams and qualifications for the teaching of Chemistry and Chemical Technology. Lecturer. More info on page About Us
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Saturday, December 6, 2014

Therefore, the excess electron pyrrole ring, while the nitrogen atom electron deficiency occurs the


Heterocyclic compounds with six members of the most common action dimension is pyridine. action dimension Pyridine has the same structure with benzene, in the form of a flat ring with five carbon atoms and one nitrogen atom. Every atom in the ring are sp 2 hybridized. Therefore pyridine having one nitrogen atom which is electronegative, the pyridine action dimension compounds are polar, action dimension whereas nonpolar action dimension benzene.
Pyridine can not be alkylated or acylated as in benzene by Friedel-crafts reaction. Pyridine can be substituted by bromine only at high temperature in the vapor phase so that the suspected reaction proceeds through formation of free radicals. Substitution reaction occurs at carbon position number 3.
Kuinolina is a heterocyclic ring which has a similar structure integrated naphthalene, but distinguished presence of the nitrogen atom at position 1 in the ring. The isokuinolina are positional isomers of kuinolina that have a nitrogen atom in the position-2. action dimension
Pyrrole, furan, action dimension and thiophene has 5 members in the ring and are aromatic. This is due to the nature of the aromatic ring of the five members in donating two electrons form a pi bond, as in benzene. Although pyrrole containing nitrogen atoms in the ring, but not alkaline as pyridine or other amines. action dimension This is due to the lone pair on the nitrogen atom has been donated to the ring to form a pi bond.
Therefore, the excess electron pyrrole ring, while the nitrogen atom electron deficiency occurs then the pyrrole partial polarization charge. Consequently, pyrrole is polar. Just as in benzene, aromatic compound which has five members can react through action dimension substitution reactions. Example:
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